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Russian
Federation on readmission and is carried out in accordance with the legislation of the Russian Federation on citizenship of the Russian Federation. Information characterizing the physiological and biological characteristics of a person, on the basis of which it is possible to establish his identity (biometric personal data), can be processed without the consent of the subject of personal data in connection with the implementation of international agreements of the Russian Federation on readmission, administration of justice and execution of judicial acts, compulsory state fingerprinting registration, as well as in cases stipulated by the legislation of the Russian Federation on defense, security, anti-terrorism, transport security, anti-corruption, operational investigative activities, public service, as well as in cases stipulated by the criminal-executive legislation of Russia, the legislation of Russia on the procedure for leaving the Russian Federation and entering the Russian Federation, citizenship of the Russian Federation and notaries.
583: – used to diagnose or rule out a specific genetic or chromosomal condition. In many cases, genetic testing is used to confirm a diagnosis when a particular condition is suspected based on physical mutations and symptoms. Diagnostic testing can be performed at any time during a person's life, but is not available for all genes or all genetic conditions. The results of a diagnostic test can influence a person's choices about health care and the management of the disease. For example, people with a family history of polycystic kidney disease (PKD) who experience pain or tenderness in their abdomen, blood in their urine, frequent urination, pain in the sides, a urinary tract infection or kidney stones may decide to have their genes tested and the result could confirm the diagnosis of PKD. Despite the several implications of genetic testing in conditions such as epilepsy or neurodevelopmental disorders, many patients (specially adults) do not have access to these modern diagnostic approaches, showing a relevant diagnostic gap.
674: – determines the influence of genetic variation on drug response. When a person has a disease or health condition, pharmacogenomics can examine an individual's genetic makeup to determine what medicine and what dosage would be the safest and most beneficial to the patient. In the human population, there are approximately 11 million single nucleotide polymorphisms (SNPs) in people's genomes, making them the most common variations in the human genome. SNPs reveal information about an individual's response to certain drugs. This type of genetic testing can be used for cancer patients undergoing chemotherapy. A sample of the cancer tissue can be sent in for genetic analysis by a specialized lab. After analysis, information retrieved can identify mutations in the tumor which can be used to determine the best treatment option.
557: – used just after birth to identify genetic disorders that can be treated early in life. A blood sample is collected with a heel prick from the newborn 24–48 hours after birth and sent to the lab for analysis. In the United States, newborn screening procedure varies state by state, but all states by law test for at least 21 disorders. If abnormal results are obtained, it does not necessarily mean the child has the disorder. Diagnostic tests must follow the initial screening to confirm the disease. The routine testing of infants for certain disorders is the most widespread use of genetic testing—millions of babies are tested each year in the United States. All states currently test infants for
664:. Hereditary breast cancer along with ovarian cancer syndrome are caused by gene alterations in the genes BRCA1 and BRCA2. Major cancer types related to mutations in these genes are female breast cancer, ovarian, prostate, pancreatic, and male breast cancer. Li-Fraumeni syndrome is caused by a gene alteration on the gene TP53. Cancer types associated with a mutation on this gene include breast cancer, soft tissue sarcoma, osteosarcoma (bone cancer), leukemia and brain tumors. In the Cowden syndrome there is a mutation on the PTEN gene, causing potential breast, thyroid or endometrial cancer. Presymptomatic testing can determine whether a person will develop a genetic disorder, such as
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638:, which removes a sample of fluid from the mother's amniotic sac 15 to 20 or more weeks into pregnancy. The fluid is then tested for chromosomal abnormalities such as Down syndrome (trisomy 21) and trisomy 18, which can result in neonatal or fetal death. Test results can be retrieved within 7–14 days after the test is done. This method is 99.4% accurate at detecting and diagnosing fetal chromosome abnormalities. There is a slight risk of miscarriage with this test, about 1:400. Another method of prenatal testing is
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of genetic sciences and innovative modern techniques related to profiling and genetic sequencing, in order to identify the genetic footprint and prevent the most prevalent diseases in the country, such as obesity, diabetes, hypertension, cancer, and asthma. It aims to achieve personalized treatment for each patient based on genetic factors. Additionally, a study by
Khalifa University has identified, for the first time, four genetic markers associated with type 2 diabetes among UAE citizens.
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589: – used to identify people who carry one copy of a gene mutation that, when present in two copies, causes a genetic disorder. This type of testing is offered to individuals who have a family history of a genetic disorder and to people in ethnic groups with an increased risk of specific genetic conditions. If both parents are tested, the test can provide information about a couple's risk of having a child with a genetic condition like
1067:; however, genetic tests may be conducted outside Israel. The law also forbids discrimination for employment or insurance purposes based on genetic test results. Finally, the law takes a strict approach to genetic testing on minors, which is permitted only for the purpose of finding a genetic match with someone ill for the sake of medical treatment, or to see whether the minor carries a gene related to an illness that can be prevented or postponed.
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970:, which was a fifteen-year project that was discontinued in 2020. Over one million people participated in the DNA sampling from more than 140 countries, which made the project the largest of its kind ever conducted. The project asked for DNA samples from indigenous people as well as the general public, which spurred political controversy among some indigenous groups, leading to the coining of the term "biocolonialism".
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legal reasons, health care providers should be cautious in providing minors with predictive genetic testing without the involvement of parents or guardians. Within the guidelines set by AAP and ACMG, health care providers have an obligation to inform parents or guardians on the implication of test results. AAP and ACMG state that any type of predictive genetic testing should be offered with
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642:(CVS). Chorionic villi are projections from the placenta that carry the same genetic makeup as the baby. During this method of prenatal testing, a sample of chorionic villi is removed from the placenta to be tested. This test is performed 10–13 weeks into pregnancy and results are ready 7–14 days after the test was done. Another test using blood taken from the fetal umbilical cord is
698: – uses special DNA markers to identify the same or similar inheritance patterns between related individuals. Based on the fact that we all inherit half of our DNA from the father, and half from the mother, DNA scientists test individuals to find the match of DNA sequences at some highly differential markers to draw the conclusion of relatedness.
962:. These companies will send the consumer a kit at their home address, with which they will provide a saliva sample for their lab to analyze. The company will then send back the consumer's results in a few weeks, which is a breakdown of their ancestral heritage and possible health risks that accompany it. Other companies, like
1028:(GDPR). The GDPR is a set of rules/regulations that helps an individual take control of their data that is collected, used, and stored digitally or in a structured filing system on paper, and restricts a company's use of personal data. The regulation also applies to companies that offer products/services outside the EU.
901:-predictive genetic test for breast cancer stated: "There is no stronger antidote for fear than information." Apart from rare diseases that are directly caused by specific, single-gene mutation, diseases "have complicated, multiple genetic links that interact strongly with personal environment, lifestyle, and behavior."
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From the date that a sample is taken, results may take weeks to months, depending upon the complexity and extent of the tests being performed. Results for prenatal testing are usually available more quickly because time is an important consideration in making decisions about a pregnancy. Prior to the
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passed the
Genetic Information Law in 2000, becoming one of the first countries to establish a regulatory framework for the conducting of genetic testing and genetic counseling and for the handling and use identified genetic information. Under the law, genetic tests must be done in labs accredited by
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By the end of 2021, the UAE Genome
Project will be in full swing, as part of the National Innovation Strategy, establishing strategic partnerships with top medical research centers, and making sustainable investments in healthcare services. The project aims to prevent genetic diseases through the use
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Genetic testing is often done as part of a genetic consultation and as of mid-2008 there were more than 1,200 clinically applicable genetic tests available. Once a person decides to proceed with genetic testing, a medical geneticist, genetic counselor, primary care doctor, or specialist can order the
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procedure. Pre-implantation testing is used when individuals try to conceive a child through in vitro fertilization. Eggs from the woman and sperm from the man are removed and fertilized outside the body to create multiple embryos. The embryos are individually screened for abnormalities, and the ones
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gland). People with PKU do not have an enzyme needed to process the amino acid phenylalanine, which is responsible for normal growth in children and normal protein use throughout their lifetime. If there is a buildup of too much phenylalanine, brain tissue can be damaged, causing developmental delay.
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decisions. Although GINA protects against genetic discrimination, Section 210 of the law states that once the disease has manifested, employers can use the medical information and not be in violation of the law, even if the condition has a genetic basis. The legislation, the first of its kind in the
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DTC genetic testing involves many of the same risks associated with any genetic test. One of the more obvious and dangerous of these is the possibility of misreading of test results. Without professional guidance, consumers can potentially misinterpret genetic information, causing them to be deluded
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The physical risks associated with most genetic tests are very small, particularly for those tests that require only a blood sample or buccal smear (a procedure that samples cells from the inside surface of the cheek). The procedures used for prenatal testing carry a small but non-negligible risk of
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The variety of genetic tests has expanded throughout the years. Early forms of genetic testing which began in the 1950s involved counting the number of chromosomes per cell. Deviations from the expected number of chromosomes (46 in humans) could lead to a diagnosis of certain genetic conditions such
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Many of the risks associated with genetic testing involve the emotional, social, or financial consequences of the test results. People may feel angry, depressed, anxious, or guilty about their results. The potential negative impact of genetic testing has led to an increasing recognition of a "right
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Predictive and presymptomatic testing – used to detect gene mutations associated with disorders that appear after birth, often later in life. These tests can be helpful to people who have a family member with a genetic disorder, but who have no features of the disorder themselves at
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of children in the United States. Their guidelines state that performing pediatric genetic testing should be in the best interest of the child. AAP and ACMG recommend holding off on genetic testing for late-onset conditions until adulthood, unless diagnosing genetic disorders during childhood can
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In Israel, DNA testing is used to determine if people are eligible for immigration. The policy where "many Jews from the former Soviet Union (FSU) are asked to provide DNA confirmation of their Jewish heritage in the form of paternity tests in order to immigrate as Jews and become citizens under
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and home kit genetic tests because of concerns regarding the accuracy, interpretation and oversight of test content. Guidelines also state that parents or guardians should be encouraged to inform their child of the results from the genetic test if the minor is of appropriate age. For ethical and
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Russian law provides that the processing of special categories of personal data relating to race, nationality, political views, religious or philosophical beliefs, health status, intimate life is allowed if it is necessary in connection with the implementation of international agreements of the
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Another limitation to genetic testing for a hereditary linked cancer, is the variants of unknown clinical significance. Because the human genome has over 22,000 genes, there are 3.5 million variants in the average person's genome. These variants of unknown clinical significance means there is a
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acquire their patient's permission and then order the desired test, which may or may not be covered by health insurance. DTC genetic tests, however, allow consumers to bypass this process and purchase DNA tests themselves. DTC genetic testing can entail primarily genealogical/ancestry-related
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for legal purposes. Unlike the tests described above, forensic testing is not used to detect gene mutations associated with disease. This type of testing can identify crime or catastrophe victims, rule out or implicate a crime suspect, or establish biological relationships between people (for
828:(DTC) genetic testing (also called at-home genetic testing) is a type of genetic test that is accessible directly to the consumer without having to go through a health care professional. Usually, to obtain a genetic test, health care professionals such as physicians, nurse practitioners, or
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Genetic testing can provide only limited information about an inherited condition. The test often can't determine if a person will show symptoms of a disorder, how severe the symptoms will be, or whether the disorder will progress over time. Another major limitation is the lack of treatment
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in employment or insurance is also a concern. Some individuals avoid genetic testing out of fear it will affect their ability to purchase insurance or find a job. Health insurers do not currently require applicants for coverage to undergo genetic testing, and when insurers encounter genetic
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In June 2013 the US Supreme Court issued two rulings on human genetics. The Court struck down patents on human genes, opening up competition in the field of genetic testing. The
Supreme Court also ruled that police were allowed to collect DNA from people arrested for serious offenses.
814:—a discovery of some possible problem found while looking for something else. In 2013 the American College of Medical Genetics and Genomics (ACMG) recommended that certain genes always be included any time a genomic sequencing was done, and that labs should report the results.
668:(an iron overload disorder), before any signs or symptoms appear. The results of predictive and presymptomatic testing can provide information about a person's risk of developing a specific disorder, help with making decisions about medical care and provide a better prognosis.
539:(cffDNA) testing – a non-invasive (for the fetus) test. It is performed on a sample of venous blood from the mother, and can provide information about the fetus early in pregnancy. As of 2015 it is the most sensitive and specific screening test for
626:'s genes or chromosomes before birth. This type of testing is offered to couples with an increased risk of having a baby with a genetic or chromosomal disorder. In some cases, prenatal testing can lessen a couple's uncertainty or help them decide whether to
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Research testing – includes finding unknown genes, learning how genes work and advancing understanding of genetic conditions. The results of testing done as part of a research study are usually not available to patients or their healthcare
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DTC genetic testing has been controversial due to outspoken opposition within the medical community. Critics of DTC genetic testing argue against the risks involved in several steps of the testing process, such as the unregulated advertising and
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Some advertising for DTC genetic testing has been criticized as conveying an exaggerated and inaccurate message about the connection between genetic information and disease risk, utilizing emotions as a selling factor. An advertisement for a
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of their database by police investigating a murder. The warrantless search led to a search warrant to force the gathering of a DNA sample from a New
Orleans filmmaker; however he turned out not to be a match for the suspected killer.
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A genetics professional can explain in detail the benefits, risks, and limitations of a particular test. It is important that any person who is considering genetic testing understand and weigh these factors before making a decision.
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Under the
Genetic Information Law as of 2019, commercial DNA tests are not permitted to be sold directly to the public, but can be obtained with a court order, due to data privacy, reliability, and misinterpretation concerns.
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for specific conditions, or gain information that can be used to customize medical treatments based on an individual's genetic makeup. Genetic testing can also be used to determine biological relatives, such as a child's
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As part of its healthcare system, Estonia is offering all of its residents genome-wide genotyping. This will be translated into personalized reports for use in everyday medical practice via the national e-health portal.
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Within the framework of this program, it is also planned to include the peoples of neighboring countries, which are the main source of migration, into the genogeographic study on the basis of existing collections.
2812:"Deep Ancestry: Inside the Genographic Project Wells Spencer . Deep Ancestry: Inside the Genographic Project. 2006. National Geographic Society. Washington, DC. $ 12.95, paperback. 247 pp. ISBN 13: 978-1426201189"
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may be swished in the mouth to collect the cells. The sample is sent to a laboratory where technicians look for specific changes in chromosomes, DNA, or proteins, depending on the suspected disorders, often using
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The aim is to minimise health problems by warning participants most at risk of conditions such as cardiovascular disease and diabetes. It is also hoped that participants who are given early warnings will adopt
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not to know". In some cases, genetic testing creates tension within a family because the results can reveal information about other family members in addition to the person who is tested. The possibility of
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reduce morbidity or mortality (e.g., to start early intervention). Testing asymptomatic children who are at risk of childhood onset conditions can also be warranted. Both AAP and ACMG discourage the use of
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439:. Genetic testing of plants and animals can be used for similar reasons as in humans (e.g. to assess relatedness/ancestry or predict/diagnose genetic disorders), to gain information used for
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844:. Possible additional risks of DTC genetic testing are the lack of governmental regulation, the potential misinterpretation of genetic information, issues related to testing minors,
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information, it is subject to the same confidentiality protections as any other sensitive health information. In the United States, the use of genetic information is governed by the
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that will result from the better understanding of human heredity the rapid expansion of genetic risk assessment by genetic testing which would be facilitated by this project.
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1926:
1850:"Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies"
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Aledo-Serrano A, García-Morales I, Toledano R, Jiménez-Huete A, Parejo B, Anciones C, et al. (October 2020). "Diagnostic gap in genetic epilepsies: A matter of age".
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All policy statements from the
American Academy of Pediatrics automatically expire 5 years after publication unless reaffirmed, revised, or retired at or before that time
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testing, the doctor or genetic counselor who is requesting a particular test can provide specific information about the cost and time frame associated with that test.
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the time of testing. Predictive testing can identify mutations that increase a person's chances of developing disorders with a genetic basis, such as certain types of
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487:, there are tests available for more than 2,000 genetic conditions, and one study estimated that as of 2018 there were more than 68,000 genetic tests on the market.
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of chromosome structure and diagnosis of genetic disorders that involved large structural rearrangements. In addition to analyzing whole chromosomes (
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prohibits group health plans and health insurers from denying coverage to a healthy person or charging that person higher premiums based solely on a
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856:. As of 2019, the tests that have received marketing authorization by the FDA include 23andMe's genetic health risk reports for select variants of
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966:, have conducted public DNA surveys in an effort to better understand global ancestry and heritage. In 2005, National Geographic launched the
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DNA studies have been criticised for a range of methodological problems and providing misleading, interpretations on racial classifications.
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uses a small brush or cotton swab to collect a sample of cells from the inside surface of the cheek. Alternatively, a small amount of saline
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change in the DNA sequence, however the increase for cancer is unclear because it is unknown if the change affects the gene's function.
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Newborn screening can detect the presence of PKU, allowing children to be placed on special diets to avoid the effects of the disorder.
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848:, and downstream expenses for the public health care system. In the United States, most DTC genetic test kits are not reviewed by the
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reports that test for selected variants associated with metabolism of certain pharmaceutical compounds, a carrier screening test for
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32:
This article is about genetic tests for disease and ancestry or biological relationships. For use in genealogy and archaeology, see
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Holtzman NA, Murphy PD, Watson MS, Barr PA (October 1997). "Predictive genetic testing: from basic research to clinical practice".
840:. Possible benefits of DTC genetic testing are the accessibility of tests to consumers, promotion of proactive healthcare, and the
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1332:"UC Davis Veterinary Genetics Laboratory | Animal DNA testing | forensic testing | animal genetic research and diagnostics"
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King E, Mahon SM (October 2017). "Genetic
Testing: Challenges and Changes in Testing for Hereditary Cancer Syndromes".
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to developing a disease in the future. The legislation also bars employers from using genetic information when making
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2724:"New Orleans filmmaker cleared in cold-case murder; false positive highlights limitations of familial DNA searching"
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losing the pregnancy (miscarriage) because they require a sample of amniotic fluid or tissue from around the fetus.
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Hunter DJ, Khoury MJ, Drazen JM (January 2008). "Letting the genome out of the bottle--will we get our wish?".
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There are a variety of DTC genetic tests, ranging from tests for breast cancer alleles to mutations linked to
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2406:"Where are you going, where have you been: a recent history of the direct-to-consumer genetic testing market"
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889:, the potential reselling of genetic data to third parties, and the overall lack of governmental oversight.
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With regard to genetic testing and information in general, legislation in the United States called the
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3177:[The UAE promises to complete the strategic health project for the country’s people in 2021].
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2267:"The Geographical Origins and Population Relationships of Early Ancient Egyptians" In Egypt in Africa
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2571:"Valuable Genomes: Taxonomy and Archetypes of Business Models in Direct-to-Consumer Genetic Testing"
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762:. The laboratory reports the test results in writing to a person's doctor or genetic counselor.
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2622:"Policy Guidance for Direct-to-Consumer Genetic Testing Services: Framework Development Study"
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structure. Genetic testing can also include measuring the results of genetic changes, such as
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screening tests are done on a small blood sample obtained by pricking the baby's heel with a
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2895:"Genetic discrimination: emerging ethical challenges in the context of advancing technology"
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which can identify changes at the level of individual genes, parts of genes, or even single
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output. In a medical setting, genetic testing can be used to diagnose or rule out suspected
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2990:"Administration News: President Bush Signs Genetic Nondiscrimination Legislation Into Law"
2019:
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Antoniou A, Pharoah PD, Narod S, Risch HA, Eyfjord JE, Hopper JL, et al. (May 2003).
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Eltis D, Bradley KR, Perry C, Engerman SL, Cartledge P, Richardson D (12 August 2021).
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Fallat ME, Katz AL, Mercurio MR, Moon MR, Okun AL, Webb SA, et al. (March 2013).
3308:. The National Academies Collection: Reports funded by National Institutes of Health.
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745:(the fluid that surrounds a fetus during pregnancy), or other tissue. For example, a
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3519:"What is the cost of genetic testing, and how long does it take to get the results?"
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Articles 10 and 11 of the
Federal Law of July 27, 2006 No. 152-FZ "On Personal Data"
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2883:, Executive Office of the President, Office of Management and Budget, 27 April 2007
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Nisbet MC (2019). "DNA Is Not Destiny: Challenging the Hype over Genetic Testing".
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Effective as of 25 May 2018, companies that process genetic data must abide by the
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What is the cost of genetic testing, and how long does it take to get the results?
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2182:"Personal gene maps: Is there such a thing as too much information about our DNA?"
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2680:"Limitations of Direct-to-Consumer Advertising for Clinical Genetic Testing,"
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Thiebes S, Toussaint PA, Ju J, Ahn JH, Lyytinen K, Sunyaev A (January 2020).
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Ancient Egyptian society : challenging assumptions, exploring approaches
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2710:" Ancestry.com Hands Over Client DNA Test Results to Cops Without a Warrant"
2201:"What should be done with unsettling 'incidental findings' in gene screens?"
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Hunter ME, Hoban SM, Bruford MW, Segelbacher G, Bernatchez L (August 2018).
459:). In the 1970s, a method to stain specific regions of chromosomes, called
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3276:"Want to fully understand your family genealogy? Not without a court order"
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on April 24, 2008, on a vote of 95–0, and was signed into law by President
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3015:
2910:
2547:
2476:"23andMe gets FDA approval to report breast cancer risk without a doctor"
1225:
992:
935:
3372:"Ethical and policy issues in genetic testing and screening of children"
2512:
2333:. Vol. 2, AD 500-AD 1420. Cambridge University Press. p. 150.
1439:
Durmaz AA, Karaca E, Demkow U, Toruner G, Schoumans J, Cogulu O (2015).
634:, however. One method of performing a prenatal genetic test involves an
4304:
3967:
1104:
939:
795:(GINA) (see discussion below in the section on government regulation).
630:
the pregnancy. It cannot identify all possible inherited disorders and
566:
504:
496:
480:
399:
207:
121:
101:
76:
3806:
3525:. Bethesda (MD): National Library of Medicine (US). November 15, 2016.
3145:"Problems of Using DNA Test for Family Reunification and Repatriation"
2251:
2219:
2026:. Bethesda (MD): National Library of Medicine (US). November 15, 2016.
1404:
4616:
4583:
4458:
4117:
4110:
4049:
4044:
4003:
3985:
3759:
2621:
950:
Genetic testing has also been taken on by private companies, such as
908:
754:
704: – used to determine ancestry or ethnic heritage for
520:
516:
464:
460:
164:
3606:
3209:
3175:"الإمارات تعد بإنجاز المشروع الصحي الاستراتيجي لأبنــاء الدولة 2021"
1795:"Genetic testing Why it's done - Tests and Procedures - Mayo Clinic"
4606:
4573:
4376:
4371:
4248:
3507:
Is It Possible to Make Aliyah to Israel on the Basis of a DNA Test?
3075:
2772:"Estonia launches genetic-testing program for 8% of its population"
2305:
10.1002/1520-6505(2001)10:1<34::AID-EVAN1011>3.0.CO;2-P
1865:
1381:"Next-generation conservation genetics and biodiversity monitoring"
1195:
627:
512:
508:
476:
436:
223:
106:
96:
51:
3305:
Assessing Genetic Risks: Implications for Health and Social Policy
2943:"Kennedy in support of genetic information nondiscrimination bill"
2638:
2587:
2269:. Indianapolis, Ind.: Indianapolis Museum of Art. pp. 20–33.
1515:"NIH Fact Sheets - Genetic Testing: How it is Used for Healthcare"
612:
4601:
4578:
4158:
3908:
3880:
3875:
3651:
3247:
1160:
1059:
951:
853:
766:
573:
415:
3424:"Genetic citizenship: DNA testing and the Israeli Law of Return"
3301:
2966:"Genetic Discrimination by Insurers, Employers Becomes a Crime"
1895:
1893:
1664:
Beischer & MacKay's Obstetrics, Gynaecology and the Newborn
1331:
799:
strategies for many genetic disorders once they are diagnosed.
651:
524:
116:
91:
1988:. Vol. 28, no. 14. Mary Ann Liebert. pp. 6, 9.
2499:
Audeh MW (May 2008). "Letting the genome out of the bottle".
2354:
Candelora D, Ben-Marzouk N, Cooney K, eds. (31 August 2022).
1982:"Successful Genetic Tests Are Predicated on Clinical Utility"
1378:
1103:(ACMG) have provided new guidelines for the ethical issue of
730:
656:
623:
2620:
Onstwedder SM, Jansen ME, Cornel MC, Rigter T (2024-07-17).
2619:
1890:
1441:"Evolution of genetic techniques: past, present, and beyond"
833:
information, health and trait-related information, or both.
3302:
Andrews LB, Fullarton JE, Holtzman NA, Motulsky AG (1994).
1612:"Recent advances in prenatal genetic screening and testing"
1084:
1012:
on May 21, 2008. It went into effect on November 21, 2009.
852:, with the exception of a few tests offered by the company
738:
734:
616:
Small amounts of the chorionic villi are sampled during CVS
523:
for clinical purposes." It can provide information about a
3106:"It's your Data - Take Control: Data Protection in the EU"
2358:. Abingdon, Oxon: Taylor & Francis. pp. 101–122.
2353:
2828:
10.3398/1527-0904(2008)68[260:daitgp]2.0.co;2
2753:"Estonia offering 100,000 residents free genetic testing"
2326:
1847:
1438:
1186:
Pre-implantation genetic diagnosis to avoid birth defects
500:
471:), genetic testing has expanded to include the fields of
403:
395:
86:
81:
3472:"'Who is a Jew?' can now be answered by genetic testing"
2892:
2020:"What are the risks and limitations of genetic testing?"
1566:
1660:
1079:
Three to five percent of the funding available for the
3545:
What are the risks and limitations of genetic testing?
3369:
3572:
United States Department of Health and Human Services
3550:
United States Department of Health and Human Services
2786:"At-home DNA test kits for 2022 | Medical News Today"
2568:
820:
3891:
List of varieties of genetically modified maize/corn
3490:"Should Jewishness be determined by a genetic test?"
1731:. Mayo Foundation for Medical Education and Research
1693:
1691:
3076:"Processing of special categories of personal data"
2121:"Genetic Information and Medical Expense Insurance"
2039:"The right not to know: an autonomy based approach"
1824:
John A. Haugen Associates Obstetrics and Gynecology
2893:Chapman CR, Mehta KS, Parent B, Caplan AL (2020).
2533:
2386:. Bethesda (MD): National Library of Medicine (US)
1705:. Bethesda (MD): National Library of Medicine (US)
608:without abnormalities are implanted in the uterus.
2403:
1979:
1901:"Genetic Testing for Hereditary Cancer Syndromes"
1688:
4629:
3350:"New Guidelines for Genetic Testing in Children"
2463:. U.S. Food and Drug Administration. 2018-11-03.
2404:Borry P, Cornel MC, Howard HC (September 2010).
2217:
1544:"10 New Genetic Tests Reach the Market Each Day"
654:. For example, an individual with a mutation in
435:, or be used to broadly predict an individual's
3421:
3050:"Justices Allow DNA Collection After an Arrest"
919:
622: – used to detect changes in a
2858:"Indigenous Peoples Council on Biocolonialism"
2289:
2106:"Insurance Fears Lead Many to Shun DNA Tests,"
1609:
3822:
3622:
3365:
3363:
2380:"What is direct-to-consumer genetic testing?"
2292:"Apportionment of racial diversity: A review"
1973:
1792:
1722:
1434:
1432:
1308:"The limits of ancestry DNA tests, explained"
507:in order to detect heritable disease-related
483:"letters" of DNA sequence. According to the
368:
2886:
2527:
2492:
2451:
2449:
1986:Genetic Engineering & Biotechnology News
1090:
4464:Detection of genetically modified organisms
3142:
2874:
2698:. Vol. 43, no. 4. pp. 28–30.
2179:
2085:
2014:
2012:
2010:
1560:
729:Genetic tests are performed on a sample of
463:, was developed that allowed more detailed
3829:
3815:
3629:
3615:
3360:
3100:
3098:
3096:
3020:"Justices, 9-0, Bar Patenting Human Genes"
2935:
2769:
1907:. National Institute of Health. 2013-04-22
1661:Permezel M, Walker S, Kyprianou K (2015).
1429:
945:
644:percutaneous umbilical cord blood sampling
551:Newborn heel-prick blood sample collection
527:'s genes and chromosomes throughout life.
375:
361:
3447:
3387:
3217:
3198:Molecular Genetics & Genomic Medicine
3194:"Genetics and genomic medicine in Israel"
3191:
3185:
2918:
2655:
2637:
2596:
2586:
2446:
2429:
2303:
2136:
2062:
1873:
1637:
1627:
1491:"Karyotyping | Learn Science at Scitable"
1466:
1456:
1412:
985:Genetic Information Nondiscrimination Act
793:Genetic Information Nondiscrimination Act
687: – uses DNA sequences to
678:
3341:
2198:
2007:
1667:. Elsevier Health Sciences. p. 74.
1356:"Selective breeding and gene technology"
1074:
1019:
973:
907:, a company providing DTC DNA tests for
776:
611:
603:prior to the implantation as part of an
546:
3836:
3347:
3093:
2721:
2461:Center for Drug Evaluation and Research
2264:
2220:"Race and Three Models of Human Origin"
2036:
1305:
1085:social, ethical, and legal implications
978:
14:
4630:
3273:
3044:
3014:
2691:
2330:The Cambridge World History of Slavery
3810:
3636:
3610:
3422:McGonigle IV, Herman LW (July 2015).
2809:
2498:
1654:
1610:Van den Veyver IB (28 October 2016).
1252:
1250:
911:purposes, has reportedly allowed the
561:(PKU, a genetic disorder that causes
530:
3240:
2963:
2626:Journal of Medical Internet Research
2575:Journal of Medical Internet Research
2139:Clinical Journal of Oncology Nursing
1955:Cancer Treatment Centers for America
1191:Elective genetic and genomic testing
1101:American College of Medical Genetics
716:
495:Genetic testing is "the analysis of
431:(genetic mother and father) through
3494:The Jerusalem Post | JPost.com
3476:The Jerusalem Post | JPost.com
2957:
2536:The New England Journal of Medicine
2501:The New England Journal of Medicine
2473:
2180:Wendelsdorf K (17 September 2013).
1980:Allingham-Hawkins D (August 2008).
24:
4494:Genetic use restriction technology
3428:Journal of Law and the Biosciences
2899:Journal of Law and the Biosciences
2881:Statement of Administration policy
1854:American Journal of Human Genetics
1817:
1247:
1026:General Data Protection Regulation
850:Food and Drug Administration (FDA)
821:Direct-to-consumer genetic testing
25:
4669:
3243:"A Different Kind of Inheritance"
2994:Kaiser Daily Health Policy Report
2816:Western North American Naturalist
2507:(20): 2184–5, author reply 2185.
1145:
1004:United States, was passed by the
597:Preimplantation genetic diagnosis
394:, is used to identify changes in
3559: This article incorporates
3554:
3537: This article incorporates
3532:
3161:10.34822/2312-3419-2021-1-91-100
2218:Lieberman L, Jackson FL (1995).
2086:Wendelsdorf K (1 October 2013).
1221:List of genetic genealogy topics
1083:was set aside to study the many
599: – performed on
342:
341:
228:
227:
58:
4512:Cartagena Protocol on Biosafety
3693:Single-nucleotide polymorphisms
3511:
3500:
3482:
3464:
3415:
3348:Rochman B (February 21, 2013).
3295:
3267:
3234:
3167:
3149:Surgut State University Journal
3136:
3127:
3068:
3038:
3008:
2982:
2850:
2803:
2778:
2770:Nesathurai A (April 11, 2018).
2763:
2745:
2715:
2702:
2685:
2672:
2613:
2562:
2467:
2397:
2372:
2347:
2320:
2290:Brown RA, Armelagos GJ (2001).
2283:
2258:
2211:
2192:
2173:
2130:
2114:
2098:
2079:
2030:
1943:
1919:
1841:
1820:"The Facts on Prenatal Testing"
1811:
1786:
1743:
1716:
1603:
1536:
4653:Alternatives to animal testing
3796:Human Genome Diversity Project
2298:. 10, Issue 1 (34–40): 34–40.
1507:
1483:
1372:
1348:
1324:
1299:
1286:American Pregnancy Association
1274:
1097:American Academy of Pediatrics
879:
842:privacy of genetic information
13:
1:
4274:Somatic cell nuclear transfer
3755:Genome-wide association study
3181:(in Arabic). 4 December 2017.
3000:. 22 May 2008. Archived from
2410:Journal of Community Genetics
2236:10.1525/aa.1995.97.2.02a00030
2199:Powledge TM (24 March 2015).
2125:American Academy of Actuaries
1957:. Rising Tide. Archived from
1629:10.12688/f1000research.9215.1
1445:BioMed Research International
1241:
1142:" has generated controversy.
924:
893:about their personal health.
660:has a 65% cumulative risk of
485:National Institutes of Health
3786:International HapMap Project
3599:Resources in other libraries
1931:American Medical Association
1581:10.1126/science.278.5338.602
1262:American Medical Association
1053:
1031:
920:Governmental genetic testing
36:. For use in forensics, see
7:
1764:10.1016/j.yebeh.2020.107266
1725:"Polycystic Kidney Disease"
1154:
447:in endangered populations.
10:
4674:
3192:Zlotogora J (March 2014).
2457:"Direct-to-Consumer Tests"
2037:Andorno R (October 2004).
1951:"Genomic Tumor Assessment"
1129:or health care providers.
443:, or for efforts to boost
31:
4597:
4566:
4520:
4502:
4449:
4419:
4387:
4332:Genetically modified food
4324:
4317:
4287:
4234:
4225:
4188:
4141:
4091:
4082:
4012:
3994:
3976:
3958:
3935:
3917:
3899:
3866:
3857:
3844:
3773:
3742:
3711:
3665:
3644:
3594:Resources in your library
2682:JAMA.2002; 288: 1762-1767
2422:10.1007/s12687-010-0023-z
2296:Evolutionary Anthropology
2043:Journal of Medical Ethics
1905:National Cancer Institute
1385:Evolutionary Applications
1216:List of genetic disorders
1132:
1091:Pediatric genetic testing
1044:
640:chorionic villus sampling
503:), proteins, and certain
406:analysis as an output of
2998:Kaiser Family Foundation
2790:www.medicalnewstoday.com
2728:The New Orleans Advocate
2205:Genetic Literacy Project
2186:Genetic Literacy Project
2092:Genetic Literacy Project
1306:Resnick B (2019-01-28).
490:
3750:Whole genome sequencing
3683:Human genetic variation
3523:Genetics Home Reference
3274:Keyser Z (2019-03-30).
2964:Keim B (May 21, 2008).
2384:Genetics Home Reference
2224:American Anthropologist
2151:10.1188/17.cjon.589-598
2055:10.1136/jme.2002.001578
2024:Genetics Home Reference
1752:Epilepsy & Behavior
1703:Genetics Home Reference
946:Private genetic testing
565:if left untreated) and
3561:public domain material
3539:public domain material
3389:10.1542/peds.2012-3680
3143:Mirolyubova S (2021).
1201:Full genome sequencing
989:genetic predisposition
874:late-onset Alzheimer's
788:genetic discrimination
689:identify an individual
679:Non-diagnostic testing
617:
605:in vitro fertilization
552:
4658:Personalized medicine
3945:Roundup ready soybean
3719:Personalized medicine
3310:Institute of Medicine
3241:Even D (2009-10-22).
2810:Duane J (June 2008).
1181:Personalized medicine
1075:Children and religion
1020:In the European Union
974:Government regulation
777:Risks and limitations
722:test after obtaining
702:Genealogical DNA test
615:
550:
433:DNA paternity testing
328:Personalized medicine
322:Personalized medicine
185:Quantitative genetics
180:Mendelian inheritance
34:genealogical DNA test
4484:Reverse transfection
4259:Genetic transduction
3791:1000 Genomes Project
3781:Human Genome Project
3729:Genetic epidemiology
2548:10.1056/NEJMp0708162
1107:genetic testing and
1081:Human Genome Project
1006:United States Senate
999:, job placement, or
979:In the United States
936:healthier lifestyles
810:Other risks include
692:example, paternity).
429:biological parentage
414:to measure specific
412:biochemical analysis
248:Branches of genetics
4638:Genetics techniques
4474:Genetics in fiction
4406:Genetic enhancement
4208:Hepatitis B vaccine
3838:Genetic engineering
3743:Analysis techniques
3724:Predictive medicine
3698:Identity by descent
3673:Biological specimen
3657:Biological database
3496:. 25 November 2017.
3113:European Commission
2513:10.1056/nejmc086053
2111:, February 24, 2008
1961:on 19 November 2016
1793:Mayo Clinic Staff.
1723:Mayo Clinic Staff.
1699:"Newborn Screening"
1458:10.1155/2015/461524
1397:2018EvApp..11.1029H
1336:www.vgl.ucdavis.edu
1282:"Paternity Testing"
1231:Non-paternity event
1176:Genographic Project
968:Genographic Project
964:National Geographic
812:incidental findings
572:(a disorder of the
537:Cell-free fetal DNA
218:Genetic engineering
175:Population genetics
46:Part of a series on
4584:Stem cell research
4203:Ice-minus bacteria
3440:10.1093/jlb/lsv027
2911:10.1093/jlb/lsz016
2695:Skeptical Inquirer
2265:Celenko T (1996).
2109:The New York Times
1211:Genetic counseling
1127:genetic counselors
1119:genetic counseling
1114:direct-to-consumer
1065:Ministry of Health
940:preventative drugs
913:warrantless search
830:genetic counselors
826:Direct-to-consumer
620:Prenatal diagnosis
618:
581:Diagnostic testing
553:
531:Diagnostic testing
473:molecular genetics
461:chromosome banding
441:selective breeding
190:Molecular genetics
149:History and topics
4625:
4624:
4589:Synthetic biology
4479:Human enhancement
4469:Genetic pollution
4445:
4444:
4313:
4312:
4221:
4220:
4184:
4183:
4078:
4077:
3804:
3803:
3678:De-identification
3638:Personal genomics
3580:Library resources
3478:. 3 October 2017.
3018:(June 13, 2013),
2759:. March 20, 2018.
2365:978-0-367-43463-2
2340:978-0-521-84067-5
1927:"Genetic Testing"
1575:(5338): 602–605.
1405:10.1111/eva.12661
1258:"Genetic testing"
1123:clinical genetics
747:medical procedure
717:Medical procedure
706:genetic genealogy
696:Paternity testing
555:Newborn screening
455:) or monosomy X (
445:genetic diversity
420:genetic disorders
385:
384:
112:Genetic variation
16:(Redirected from
4665:
4648:Medical genetics
4362:Dow AgroSciences
4322:
4321:
4232:
4231:
4089:
4088:
3864:
3863:
3855:
3854:
3831:
3824:
3817:
3808:
3807:
3734:Pharmacogenomics
3703:Genetic disorder
3631:
3624:
3617:
3608:
3607:
3575:
3558:
3557:
3553:
3536:
3535:
3527:
3526:
3515:
3509:
3504:
3498:
3497:
3486:
3480:
3479:
3468:
3462:
3461:
3451:
3419:
3413:
3412:
3391:
3367:
3358:
3357:
3345:
3339:
3338:
3336:
3334:
3299:
3293:
3292:
3290:
3288:
3271:
3265:
3264:
3262:
3260:
3251:. Archived from
3238:
3232:
3231:
3221:
3189:
3183:
3182:
3171:
3165:
3164:
3140:
3134:
3131:
3125:
3124:
3122:
3120:
3110:
3102:
3091:
3090:
3088:
3086:
3072:
3066:
3065:
3064:
3062:
3048:(June 3, 2013),
3042:
3036:
3035:
3034:
3032:
3012:
3006:
3005:
2986:
2980:
2979:
2977:
2976:
2961:
2955:
2954:
2952:
2950:
2939:
2933:
2932:
2922:
2890:
2884:
2878:
2872:
2871:
2869:
2868:
2854:
2848:
2847:
2807:
2801:
2800:
2798:
2797:
2782:
2776:
2775:
2767:
2761:
2760:
2749:
2743:
2742:
2740:
2739:
2730:. Archived from
2719:
2713:
2706:
2700:
2699:
2689:
2683:
2678:Gollust et al.,
2676:
2670:
2669:
2659:
2641:
2617:
2611:
2610:
2600:
2590:
2566:
2560:
2559:
2531:
2525:
2524:
2496:
2490:
2489:
2487:
2486:
2471:
2465:
2464:
2453:
2444:
2443:
2433:
2401:
2395:
2394:
2392:
2391:
2376:
2370:
2369:
2351:
2345:
2344:
2324:
2318:
2317:
2307:
2287:
2281:
2280:
2262:
2256:
2255:
2215:
2209:
2208:
2196:
2190:
2189:
2177:
2171:
2170:
2134:
2128:
2118:
2112:
2102:
2096:
2095:
2083:
2077:
2076:
2066:
2034:
2028:
2027:
2016:
2005:
2004:
2002:
2000:
1977:
1971:
1970:
1968:
1966:
1947:
1941:
1940:
1938:
1937:
1923:
1917:
1916:
1914:
1912:
1897:
1888:
1887:
1877:
1860:(5): 1117–1130.
1845:
1839:
1838:
1836:
1835:
1826:. Archived from
1815:
1809:
1808:
1806:
1805:
1790:
1784:
1783:
1747:
1741:
1740:
1738:
1736:
1720:
1714:
1713:
1711:
1710:
1695:
1686:
1685:
1683:
1681:
1658:
1652:
1651:
1641:
1631:
1607:
1601:
1600:
1564:
1558:
1557:
1555:
1554:
1540:
1534:
1533:
1531:
1530:
1521:. Archived from
1511:
1505:
1504:
1502:
1501:
1487:
1481:
1480:
1470:
1460:
1436:
1427:
1426:
1416:
1391:(7): 1029–1034.
1376:
1370:
1369:
1367:
1366:
1352:
1346:
1345:
1343:
1342:
1328:
1322:
1321:
1319:
1318:
1303:
1297:
1296:
1294:
1293:
1278:
1272:
1271:
1269:
1268:
1254:
1206:Exome sequencing
887:marketing claims
724:informed consent
685:Forensic testing
672:Pharmacogenomics
390:, also known as
377:
370:
363:
350:
345:
344:
240:Medical genetics
236:
231:
230:
62:
43:
42:
21:
4673:
4672:
4668:
4667:
4666:
4664:
4663:
4662:
4628:
4627:
4626:
4621:
4593:
4562:
4516:
4498:
4451:
4441:
4415:
4411:Genetic testing
4393:
4383:
4309:
4295:Recombinant DNA
4283:
4254:Electroporation
4217:
4213:Oncolytic virus
4192:
4180:
4137:
4123:Herman the Bull
4074:
4008:
3990:
3972:
3954:
3931:
3913:
3895:
3849:
3847:
3840:
3835:
3805:
3800:
3769:
3765:Genetic testing
3738:
3707:
3688:Genetic linkage
3661:
3645:Data collection
3640:
3635:
3605:
3604:
3603:
3588:
3587:
3585:Genetic testing
3583:
3564:
3555:
3542:
3533:
3530:
3517:
3516:
3512:
3505:
3501:
3488:
3487:
3483:
3470:
3469:
3465:
3420:
3416:
3368:
3361:
3346:
3342:
3332:
3330:
3320:
3300:
3296:
3286:
3284:
3272:
3268:
3258:
3256:
3239:
3235:
3210:10.1002/mgg3.73
3190:
3186:
3173:
3172:
3168:
3141:
3137:
3132:
3128:
3118:
3116:
3108:
3104:
3103:
3094:
3084:
3082:
3074:
3073:
3069:
3060:
3058:
3043:
3039:
3030:
3028:
3013:
3009:
2988:
2987:
2983:
2974:
2972:
2962:
2958:
2948:
2946:
2945:. 24 April 2008
2941:
2940:
2936:
2891:
2887:
2879:
2875:
2866:
2864:
2856:
2855:
2851:
2808:
2804:
2795:
2793:
2784:
2783:
2779:
2768:
2764:
2751:
2750:
2746:
2737:
2735:
2720:
2716:
2708:Ronald Bailey,
2707:
2703:
2690:
2686:
2677:
2673:
2618:
2614:
2567:
2563:
2532:
2528:
2497:
2493:
2484:
2482:
2480:Washington Post
2472:
2468:
2455:
2454:
2447:
2402:
2398:
2389:
2387:
2378:
2377:
2373:
2366:
2352:
2348:
2341:
2325:
2321:
2288:
2284:
2277:
2263:
2259:
2216:
2212:
2197:
2193:
2178:
2174:
2135:
2131:
2119:
2115:
2103:
2099:
2084:
2080:
2035:
2031:
2018:
2017:
2008:
1998:
1996:
1978:
1974:
1964:
1962:
1949:
1948:
1944:
1935:
1933:
1925:
1924:
1920:
1910:
1908:
1899:
1898:
1891:
1846:
1842:
1833:
1831:
1816:
1812:
1803:
1801:
1791:
1787:
1748:
1744:
1734:
1732:
1721:
1717:
1708:
1706:
1697:
1696:
1689:
1679:
1677:
1675:
1659:
1655:
1608:
1604:
1565:
1561:
1552:
1550:
1542:
1541:
1537:
1528:
1526:
1513:
1512:
1508:
1499:
1497:
1489:
1488:
1484:
1437:
1430:
1377:
1373:
1364:
1362:
1354:
1353:
1349:
1340:
1338:
1330:
1329:
1325:
1316:
1314:
1304:
1300:
1291:
1289:
1280:
1279:
1275:
1266:
1264:
1256:
1255:
1248:
1244:
1157:
1148:
1135:
1093:
1077:
1056:
1047:
1034:
1022:
981:
976:
960:Family Tree DNA
948:
927:
922:
882:
862:pharmacogenetic
846:privacy of data
838:cystic fibrosis
823:
779:
719:
681:
666:hemochromatosis
591:cystic fibrosis
587:Carrier testing
559:phenylketonuria
533:
493:
457:Turner syndrome
451:as trisomy 21 (
408:gene expression
388:Genetic testing
381:
340:
333:
332:
323:
315:
314:
313:
312:
261:
253:
252:
244:
222:
203:
195:
194:
150:
142:
141:
128:
127:
126:
70:
41:
28:
23:
22:
15:
12:
11:
5:
4671:
4661:
4660:
4655:
4650:
4645:
4640:
4623:
4622:
4620:
4619:
4614:
4609:
4604:
4598:
4595:
4594:
4592:
4591:
4586:
4581:
4576:
4570:
4568:
4567:Similar fields
4564:
4563:
4561:
4560:
4555:
4550:
4540:
4535:
4530:
4524:
4522:
4518:
4517:
4515:
4514:
4508:
4506:
4500:
4499:
4497:
4496:
4491:
4486:
4481:
4476:
4471:
4466:
4461:
4455:
4453:
4447:
4446:
4443:
4442:
4440:
4439:
4437:Gene targeting
4434:
4432:Gene knockdown
4429:
4423:
4421:
4417:
4416:
4414:
4413:
4408:
4403:
4397:
4395:
4385:
4384:
4382:
4381:
4380:
4379:
4374:
4369:
4367:DuPont Pioneer
4364:
4359:
4354:
4346:
4341:
4340:
4339:
4328:
4326:
4325:In agriculture
4319:
4315:
4314:
4311:
4310:
4308:
4307:
4302:
4297:
4291:
4289:
4285:
4284:
4282:
4281:
4276:
4271:
4269:Microinjection
4266:
4261:
4256:
4251:
4246:
4240:
4238:
4229:
4223:
4222:
4219:
4218:
4216:
4215:
4210:
4205:
4199:
4197:
4186:
4185:
4182:
4181:
4179:
4178:
4173:
4168:
4167:
4166:
4161:
4151:
4145:
4143:
4139:
4138:
4136:
4135:
4130:
4125:
4120:
4115:
4114:
4113:
4108:
4106:Knockout mouse
4097:
4095:
4086:
4080:
4079:
4076:
4075:
4073:
4072:
4067:
4062:
4057:
4052:
4047:
4042:
4037:
4032:
4027:
4022:
4016:
4014:
4010:
4009:
4007:
4006:
4000:
3998:
3992:
3991:
3989:
3988:
3982:
3980:
3974:
3973:
3971:
3970:
3964:
3962:
3956:
3955:
3953:
3952:
3947:
3941:
3939:
3933:
3932:
3930:
3929:
3923:
3921:
3915:
3914:
3912:
3911:
3905:
3903:
3897:
3896:
3894:
3893:
3888:
3883:
3878:
3872:
3870:
3861:
3852:
3842:
3841:
3834:
3833:
3826:
3819:
3811:
3802:
3801:
3799:
3798:
3793:
3788:
3783:
3777:
3775:
3774:Major projects
3771:
3770:
3768:
3767:
3762:
3757:
3752:
3746:
3744:
3740:
3739:
3737:
3736:
3731:
3726:
3721:
3715:
3713:
3709:
3708:
3706:
3705:
3700:
3695:
3690:
3685:
3680:
3675:
3669:
3667:
3666:Field concepts
3663:
3662:
3660:
3659:
3654:
3648:
3646:
3642:
3641:
3634:
3633:
3626:
3619:
3611:
3602:
3601:
3596:
3590:
3589:
3578:
3577:
3529:
3528:
3510:
3499:
3481:
3463:
3434:(2): 469–478.
3414:
3382:(3): 620–622.
3359:
3340:
3318:
3294:
3281:Jerusalem Post
3266:
3233:
3184:
3166:
3155:(31): 91–100.
3135:
3126:
3092:
3067:
3055:New York Times
3037:
3025:New York Times
3007:
3004:on 2009-03-29.
2981:
2956:
2934:
2885:
2873:
2849:
2822:(2): 260–261.
2802:
2777:
2762:
2744:
2714:
2701:
2684:
2671:
2612:
2561:
2542:(2): 105–107.
2526:
2491:
2466:
2445:
2416:(3): 101–106.
2396:
2371:
2364:
2346:
2339:
2319:
2282:
2275:
2257:
2230:(2): 231–242.
2210:
2191:
2172:
2145:(5): 589–598.
2129:
2113:
2097:
2078:
2049:(5): 435–439.
2029:
2006:
1972:
1942:
1918:
1889:
1866:10.1086/375033
1840:
1810:
1785:
1742:
1715:
1687:
1673:
1653:
1602:
1559:
1535:
1519:report.nih.gov
1506:
1495:www.nature.com
1482:
1428:
1371:
1347:
1323:
1298:
1273:
1245:
1243:
1240:
1239:
1238:
1233:
1228:
1223:
1218:
1213:
1208:
1203:
1198:
1193:
1188:
1183:
1178:
1173:
1168:
1163:
1156:
1153:
1147:
1146:Costs and time
1144:
1134:
1131:
1099:(AAP) and the
1092:
1089:
1076:
1073:
1055:
1052:
1046:
1043:
1033:
1030:
1021:
1018:
1010:George W. Bush
980:
977:
975:
972:
947:
944:
926:
923:
921:
918:
881:
878:
870:celiac disease
866:Bloom syndrome
822:
819:
778:
775:
760:DNA sequencing
743:amniotic fluid
718:
715:
714:
713:
709:
699:
693:
680:
677:
676:
675:
669:
647:
609:
594:
584:
578:
570:hypothyroidism
563:mental illness
544:
532:
529:
492:
489:
383:
382:
380:
379:
372:
365:
357:
354:
353:
352:
351:
335:
334:
331:
330:
324:
321:
320:
317:
316:
311:
310:
305:
300:
295:
290:
288:Immunogenetics
285:
280:
275:
270:
264:
263:
262:
259:
258:
255:
254:
251:
250:
243:
242:
237:
220:
215:
213:DNA sequencing
210:
204:
201:
200:
197:
196:
193:
192:
187:
182:
177:
172:
162:
157:
151:
148:
147:
144:
143:
140:
139:
134:
125:
124:
119:
114:
109:
104:
99:
94:
89:
84:
79:
73:
72:
71:
69:Key components
68:
67:
64:
63:
55:
54:
48:
47:
26:
9:
6:
4:
3:
2:
4670:
4659:
4656:
4654:
4651:
4649:
4646:
4644:
4643:Medical tests
4641:
4639:
4636:
4635:
4633:
4618:
4615:
4613:
4612:Biotechnology
4610:
4608:
4605:
4603:
4600:
4599:
4596:
4590:
4587:
4585:
4582:
4580:
4577:
4575:
4572:
4571:
4569:
4565:
4559:
4556:
4554:
4553:South America
4551:
4548:
4544:
4543:North America
4541:
4539:
4536:
4534:
4531:
4529:
4526:
4525:
4523:
4519:
4513:
4510:
4509:
4507:
4505:
4501:
4495:
4492:
4490:
4489:Transhumanism
4487:
4485:
4482:
4480:
4477:
4475:
4472:
4470:
4467:
4465:
4462:
4460:
4457:
4456:
4454:
4448:
4438:
4435:
4433:
4430:
4428:
4427:Gene knockout
4425:
4424:
4422:
4418:
4412:
4409:
4407:
4404:
4402:
4399:
4398:
4396:
4391:
4386:
4378:
4375:
4373:
4370:
4368:
4365:
4363:
4360:
4358:
4355:
4353:
4350:
4349:
4347:
4345:
4342:
4338:
4337:Controversies
4335:
4334:
4333:
4330:
4329:
4327:
4323:
4320:
4316:
4306:
4303:
4301:
4298:
4296:
4293:
4292:
4290:
4286:
4280:
4277:
4275:
4272:
4270:
4267:
4265:
4262:
4260:
4257:
4255:
4252:
4250:
4247:
4245:
4242:
4241:
4239:
4237:
4236:Inserting DNA
4233:
4230:
4228:
4224:
4214:
4211:
4209:
4206:
4204:
4201:
4200:
4198:
4196:
4191:
4187:
4177:
4174:
4172:
4169:
4165:
4162:
4160:
4157:
4156:
4155:
4152:
4150:
4147:
4146:
4144:
4142:Other animals
4140:
4134:
4131:
4129:
4126:
4124:
4121:
4119:
4116:
4112:
4109:
4107:
4104:
4103:
4102:
4099:
4098:
4096:
4094:
4090:
4087:
4085:
4081:
4071:
4068:
4066:
4063:
4061:
4058:
4056:
4053:
4051:
4048:
4046:
4043:
4041:
4038:
4036:
4033:
4031:
4028:
4026:
4023:
4021:
4018:
4017:
4015:
4011:
4005:
4002:
4001:
3999:
3997:
3993:
3987:
3984:
3983:
3981:
3979:
3975:
3969:
3966:
3965:
3963:
3961:
3957:
3951:
3948:
3946:
3943:
3942:
3940:
3938:
3934:
3928:
3925:
3924:
3922:
3920:
3916:
3910:
3907:
3906:
3904:
3902:
3898:
3892:
3889:
3887:
3884:
3882:
3879:
3877:
3874:
3873:
3871:
3869:
3865:
3862:
3860:
3856:
3853:
3851:
3843:
3839:
3832:
3827:
3825:
3820:
3818:
3813:
3812:
3809:
3797:
3794:
3792:
3789:
3787:
3784:
3782:
3779:
3778:
3776:
3772:
3766:
3763:
3761:
3758:
3756:
3753:
3751:
3748:
3747:
3745:
3741:
3735:
3732:
3730:
3727:
3725:
3722:
3720:
3717:
3716:
3714:
3710:
3704:
3701:
3699:
3696:
3694:
3691:
3689:
3686:
3684:
3681:
3679:
3676:
3674:
3671:
3670:
3668:
3664:
3658:
3655:
3653:
3650:
3649:
3647:
3643:
3639:
3632:
3627:
3625:
3620:
3618:
3613:
3612:
3609:
3600:
3597:
3595:
3592:
3591:
3586:
3581:
3576:
3573:
3569:
3568:
3562:
3551:
3547:
3546:
3540:
3524:
3520:
3514:
3508:
3503:
3495:
3491:
3485:
3477:
3473:
3467:
3459:
3455:
3450:
3445:
3441:
3437:
3433:
3429:
3425:
3418:
3411:
3407:
3403:
3399:
3395:
3390:
3385:
3381:
3377:
3373:
3366:
3364:
3355:
3351:
3344:
3329:
3325:
3321:
3319:0-309-04798-6
3315:
3311:
3307:
3306:
3298:
3283:
3282:
3277:
3270:
3255:on 2024-01-16
3254:
3250:
3249:
3244:
3237:
3229:
3225:
3220:
3215:
3211:
3207:
3203:
3199:
3195:
3188:
3180:
3176:
3170:
3162:
3158:
3154:
3150:
3146:
3139:
3130:
3114:
3107:
3101:
3099:
3097:
3081:
3077:
3071:
3057:
3056:
3051:
3047:
3041:
3027:
3026:
3021:
3017:
3011:
3003:
2999:
2995:
2991:
2985:
2971:
2967:
2960:
2944:
2938:
2930:
2926:
2921:
2916:
2912:
2908:
2905:(1): lsz016.
2904:
2900:
2896:
2889:
2882:
2877:
2863:
2859:
2853:
2845:
2841:
2837:
2833:
2829:
2825:
2821:
2817:
2813:
2806:
2791:
2787:
2781:
2773:
2766:
2758:
2754:
2748:
2734:on 2016-07-11
2733:
2729:
2725:
2722:Jim Mustian.
2718:
2711:
2705:
2697:
2696:
2688:
2681:
2675:
2667:
2663:
2658:
2653:
2649:
2645:
2640:
2639:10.2196/47389
2635:
2631:
2627:
2623:
2616:
2608:
2604:
2599:
2594:
2589:
2588:10.2196/14890
2584:
2581:(1): e14890.
2580:
2576:
2572:
2565:
2557:
2553:
2549:
2545:
2541:
2537:
2530:
2522:
2518:
2514:
2510:
2506:
2502:
2495:
2481:
2477:
2470:
2462:
2458:
2452:
2450:
2441:
2437:
2432:
2427:
2423:
2419:
2415:
2411:
2407:
2400:
2385:
2381:
2375:
2367:
2361:
2357:
2350:
2342:
2336:
2332:
2331:
2323:
2315:
2311:
2306:
2301:
2297:
2293:
2286:
2278:
2272:
2268:
2261:
2253:
2249:
2245:
2241:
2237:
2233:
2229:
2225:
2221:
2214:
2206:
2202:
2195:
2187:
2183:
2176:
2168:
2164:
2160:
2156:
2152:
2148:
2144:
2140:
2133:
2126:
2122:
2117:
2110:
2107:
2101:
2093:
2089:
2082:
2074:
2070:
2065:
2060:
2056:
2052:
2048:
2044:
2040:
2033:
2025:
2021:
2015:
2013:
2011:
1995:
1991:
1987:
1983:
1976:
1960:
1956:
1952:
1946:
1932:
1928:
1922:
1906:
1902:
1896:
1894:
1885:
1881:
1876:
1871:
1867:
1863:
1859:
1855:
1851:
1844:
1830:on 2015-04-02
1829:
1825:
1821:
1814:
1800:
1796:
1789:
1781:
1777:
1773:
1769:
1765:
1761:
1757:
1753:
1746:
1730:
1726:
1719:
1704:
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308:Quantitative
278:Cytogenetics
273:Conservation
155:Introduction
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4394:diagnostics
4264:Lipofection
4025:Arabidopsis
3927:Golden rice
2127:, June 2000
1965:18 November
1911:18 November
1818:Haugen JA.
1799:Mayo Clinic
1735:18 November
1729:Mayo Clinic
1226:Michiei Oto
880:Controversy
858:BRCA1/BRCA2
505:metabolites
497:chromosomes
392:DNA testing
4632:Categories
4504:Regulation
4348:Companies
4305:Cisgenesis
4249:Biolistics
4055:Sugar beet
3968:Flavr Savr
3868:Maize/corn
3376:Pediatrics
3287:16 January
3259:16 January
3085:23 October
2975:2008-05-28
2867:2022-11-09
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2738:2015-05-06
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2632:: e47389.
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712:providers.
567:congenital
521:karyotypes
517:phenotypes
481:nucleotide
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122:Amino acid
102:Nucleotide
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4617:Bioethics
4521:Geography
4459:Transgene
4227:Processes
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3850:organisms
3760:SNP array
3333:3 October
2970:Wired.com
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2648:1438-8871
2244:0002-7294
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1109:screening
1105:pediatric
1054:In Israel
1032:In Russia
1001:promotion
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755:mouthwash
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293:Microbial
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1196:Eugenics
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465:analysis
437:ancestry
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4558:Oceania
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