-
1
-
-
85016161935
-
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)
-
MacArthur, J. et al. The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). Nucleic Acids Res. 45, D896-D901 (2017).
-
(2017)
Nucleic Acids Res.
, vol.45
, pp. D896-D901
-
-
MacArthur, J.1
-
2
-
-
84982253941
-
Analysis of protein-coding genetic variation in 60,706 humans
-
Lek, M. et al. Analysis of protein-coding genetic variation in 60,706 humans. Nature 536, 285-291 (2016).
-
(2016)
Nature
, vol.536
, pp. 285-291
-
-
Lek, M.1
-
3
-
-
85007028930
-
Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study
-
Dewey, F. E. et al. Distribution and clinical impact of functional variants in 50,726 whole-exome sequences from the DiscovEHR study. Science 354, aaf6814 (2016).
-
(2016)
Science
, vol.354
, pp. aaf6814
-
-
Dewey, F.E.1
-
4
-
-
84944441319
-
Genetic variation and the de novo assembly of human genomes
-
Chaisson, M. J., Wilson, R. K. & Eichler, E. E. Genetic variation and the de novo assembly of human genomes. Nat. Rev. Genet. 16, 627-640 (2015).
-
(2015)
Nat. Rev. Genet.
, vol.16
, pp. 627-640
-
-
Chaisson, M.J.1
Wilson, R.K.2
Eichler, E.E.3
-
6
-
-
84943171338
-
A global reference for human genetic variation
-
1000 Genomes Project Consortium et al
-
1000 Genomes Project Consortium et al. A global reference for human genetic variation. Nature 526, 68-74 (2015).
-
(2015)
Nature
, vol.526
, pp. 68-74
-
-
-
7
-
-
84991669666
-
Genomics is failing on diversity
-
Popejoy, A. B. & Fullerton, S. M. Genomics is failing on diversity. Nature 538, 161-164 (2016).
-
(2016)
Nature
, vol.538
, pp. 161-164
-
-
Popejoy, A.B.1
Fullerton, S.M.2
-
8
-
-
85042044288
-
-
United Nations Department of Economic and Social Affairs. World population prospects: the 2015 revision (UN, 2015)
-
United Nations Department of Economic and Social Affairs. World population prospects: the 2015 revision (UN, 2015).
-
-
-
-
10
-
-
33846271418
-
Merging and emerging cohorts: Necessary but not sufficient
-
Collins, F. S. & Manolio, T. A. Merging and emerging cohorts: necessary but not sufficient. Nature 445, 259 (2007).
-
(2007)
Nature
, vol.445
, pp. 259
-
-
Collins, F.S.1
Manolio, T.A.2
-
11
-
-
0024095149
-
Gm3;5,13,14 and type 2 diabetes mellitus: An association in American Indians with genetic admixture
-
Knowler, W. C., Williams, R. C., Pettitt, D. J. & Steinberg, A. G. Gm3;5,13,14 and type 2 diabetes mellitus: an association in American Indians with genetic admixture. Am. J. Hum. Genet. 43, 520-526 (1988).
-
(1988)
Am. J. Hum. Genet.
, vol.43
, pp. 520-526
-
-
Knowler, W.C.1
Williams, R.C.2
Pettitt, D.J.3
Steinberg, A.G.4
-
12
-
-
84925560093
-
After Havasupai litigation, Native Americans wary of genetic research
-
[No authors listed.]
-
[No authors listed.] After Havasupai litigation, Native Americans wary of genetic research. Am. J. Med. Genet. 152A, fm ix (2010).
-
(2010)
Am. J. Med. Genet.
, pp. 152A
-
-
-
13
-
-
37349116252
-
The continuum of translation research in genomic medicine: How can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention?
-
Khoury, M. J. et al. The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention? Genet. Med. 9, 665-674 (2007).
-
(2007)
Genet. Med.
, vol.9
, pp. 665-674
-
-
Khoury, M.J.1
-
14
-
-
79951472909
-
Charting a course for genomic medicine from base pairs to bedside
-
National Human Genome Research Institute
-
Green, E. D., Guyer, M. S. & National Human Genome Research Institute. Charting a course for genomic medicine from base pairs to bedside. Nature 470, 204-213 (2011).
-
(2011)
Nature
, vol.470
, pp. 204-213
-
-
Green, E.D.1
Guyer, M.S.2
-
15
-
-
85016023655
-
Bedside back to bench: Building bridges between basic and clinical genomic research
-
Manolio, T. A. et al. Bedside back to bench: building bridges between basic and clinical genomic research. Cell 169, 6-12 (2017).
-
(2017)
Cell
, vol.169
, pp. 6-12
-
-
Manolio, T.A.1
-
16
-
-
85026785714
-
Diversity and inclusion in genomic research: Why the uneven progress?
-
Bentley, A. R., Callier, S. & Rotimi, C. N. Diversity and inclusion in genomic research: why the uneven progress? J. Commun. Genet. 8, 255-266 (2017).
-
(2017)
J. Commun. Genet.
, vol.8
, pp. 255-266
-
-
Bentley, A.R.1
Callier, S.2
Rotimi, C.N.3
-
17
-
-
13944265645
-
Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9
-
Cohen, J. et al. Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9. Nat. Genet. 37, 161-165 (2005).
-
(2005)
Nat. Genet.
, vol.37
, pp. 161-165
-
-
Cohen, J.1
-
18
-
-
84982187833
-
Genetic misdiagnoses and the potential for health disparities
-
Manrai, A. K. et al. Genetic misdiagnoses and the potential for health disparities. N. Engl. J. Med. 375, 655-665 (2016).
-
(2016)
N. Engl. J. Med.
, vol.375
, pp. 655-665
-
-
Manrai, A.K.1
-
19
-
-
85042005215
-
-
National Institutes of Health. Population Architecture Using Genomics and Epidemiology (PAGE), phase II-study investigators (U01). National Institutes of Health: Grants & Funding
-
National Institutes of Health. Population Architecture Using Genomics and Epidemiology (PAGE), phase II-study investigators (U01). National Institutes of Health: Grants & Funding https://grants.nih.gov/grants/guide/rfa-files/RFA-HG-12-010.html (2012).
-
(2012)
-
-
-
21
-
-
85041998524
-
-
National Institutes of Health. Human Heredity and Health in Africa (H3Africa): research projects (U01). National Institutes of Health: Grants & Funding
-
National Institutes of Health. Human Heredity and Health in Africa (H3Africa): research projects (U01). National Institutes of Health: Grants & Funding https://grants.nih.gov/grants/guide/rfa-files/RFA-RM-16-015.html (2016).
-
(2016)
-
-
-
22
-
-
85042011563
-
-
National Institutes of Health. Centers for common disease genomics (UM1). National Institutes of Health: Grants & Funding
-
National Institutes of Health. Centers for common disease genomics (UM1). National Institutes of Health: Grants & Funding https://grants.nih.gov/grants/guide/rfa-files/RFA-HG-15-001.html (2014).
-
(2014)
-
-
-
24
-
-
84939422197
-
Characterizing race/ethnicity and genetic ancestry for 100,000 subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort
-
Banda, Y. et al. Characterizing race/ethnicity and genetic ancestry for 100,000 subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort. Genetics 200, 1285-1295 (2015).
-
(2015)
Genetics
, vol.200
, pp. 1285-1295
-
-
Banda, Y.1
-
25
-
-
85042007628
-
-
National Human Genome Research Institute. Genomics and health disparities lecture series. National Human Genome Research Institute
-
National Human Genome Research Institute. Genomics and health disparities lecture series. National Human Genome Research Institute https://www.genome.gov/27561525/genomics-and-health-disparities-lecture-series/(2017).
-
(2017)
-
-
-
26
-
-
85041996264
-
-
National Human Genome Research Institute & National Institute on Minority Health and Health Disparities. (Rockville
-
National Human Genome Research Institute & National Institute on Minority Health and Health Disparities. Workshop on the use of race and ethnicity in genomics and biomedical research (Rockville, 2016).
-
(2016)
Workshop on the Use of Race and Ethnicity in Genomics and Biomedical Research
-
-
-
27
-
-
2942705885
-
Genetic research and health disparities
-
Sankar, P. et al. Genetic research and health disparities. JAMA 291, 2985-2989 (2004).
-
(2004)
JAMA
, vol.291
, pp. 2985-2989
-
-
Sankar, P.1
-
28
-
-
85019474960
-
Genomics, health disparities, and missed opportunities for the nation's research agenda
-
West, K. M., Blacksher, E. & Burke, W. Genomics, health disparities, and missed opportunities for the nation's research agenda. JAMA 317, 1831-1832 (2017).
-
(2017)
JAMA
, vol.317
, pp. 1831-1832
-
-
West, K.M.1
Blacksher, E.2
Burke, W.3
-
29
-
-
84880184188
-
Genome science and health disparities: A growing success story?
-
Rotimi, C., Shriner, D. & Adeyemo, A. Genome science and health disparities: a growing success story? Genome Med. 5, 61 (2013).
-
(2013)
Genome Med.
, vol.5
, pp. 61
-
-
Rotimi, C.1
Shriner, D.2
Adeyemo, A.3
-
30
-
-
79960429419
-
Genomics for the world
-
Bustamante, C. D., Burchard, E. G. & De la Vega, F. M. Genomics for the world. Nature 475, 163-165 (2011).
-
(2011)
Nature
, vol.475
, pp. 163-165
-
-
Bustamante, C.D.1
Burchard, E.G.2
De La Vega, F.M.3
-
31
-
-
22844435315
-
Misreading race and genomics after BiDil
-
Kahn, J. Misreading race and genomics after BiDil. Nat. Genet. 37, 655-656 (2005).
-
(2005)
Nat. Genet.
, vol.37
, pp. 655-656
-
-
Kahn, J.1
-
32
-
-
12344264825
-
The use of race variables in genetic studies of complex traits and the goal of reducing health disparities: A transdisciplinary perspective
-
Shields, A. E. et al. The use of race variables in genetic studies of complex traits and the goal of reducing health disparities: a transdisciplinary perspective. Am. Psychol. 60, 77-103 (2005).
-
(2005)
Am. Psychol.
, vol.60
, pp. 77-103
-
-
Shields, A.E.1
-
33
-
-
84880139863
-
Genes, race, and culture in clinical care: Racial profiling in the management of chronic illness
-
Hunt, L. M., Truesdell, N. D. & Kreiner, M. J. Genes, race, and culture in clinical care: racial profiling in the management of chronic illness. Med. Anthropol. Q. 27, 253-271 (2013).
-
(2013)
Med. Anthropol. Q.
, vol.27
, pp. 253-271
-
-
Hunt, L.M.1
Truesdell, N.D.2
Kreiner, M.J.3
-
34
-
-
84997132288
-
Addressing social determinants of health and health inequalities
-
Adler, N. E., Glymour, M. M. & Fielding, J. Addressing social determinants of health and health inequalities. JAMA 316, 1641-1642 (2016).
-
(2016)
JAMA
, vol.316
, pp. 1641-1642
-
-
Adler, N.E.1
Glymour, M.M.2
Fielding, J.3
-
35
-
-
84891309189
-
The social determinants of health: It's time to consider the causes of the causes
-
Braveman, P. & Gottlieb, L. The social determinants of health: it's time to consider the causes of the causes. Public Health Rep. 129 (Suppl. 2), 19-31 (2014).
-
(2014)
Public Health Rep.
, vol.129
, pp. 19-31
-
-
Braveman, P.1
Gottlieb, L.2
-
36
-
-
77249089824
-
Race, socioeconomic status, and health: Complexities, ongoing challenges, and research opportunities
-
Williams, D. R., Mohammed, S. A., Leavell, J. & Collins, C. Race, socioeconomic status, and health: complexities, ongoing challenges, and research opportunities. Ann. NY Acad. Sci. 1186, 69-101 (2010).
-
(2010)
Ann. NY Acad. Sci.
, vol.1186
, pp. 69-101
-
-
Williams, D.R.1
Mohammed, S.A.2
Leavell, J.3
Collins, C.4
-
37
-
-
85033231331
-
Comparison of breast cancer molecular features and survival by African and European ancestry in the Cancer Genome Atlas
-
Huo, D. et al. Comparison of breast cancer molecular features and survival by African and European ancestry in the Cancer Genome Atlas. JAMA Oncol. http://dx.doi.org/10.1001/jamaoncol.2017.0595 (2017).
-
(2017)
JAMA Oncol
-
-
Huo, D.1
-
38
-
-
85042053632
-
-
International Cancer Genome Consortium for Medicine.. International Cancer Genome Consortium for Medicine https://icgcmed.org/
-
International Cancer Genome Consortium for Medicine. Linking genomics to clinical information. International Cancer Genome Consortium for Medicine https://icgcmed.org/(2017).
-
(2017)
Linking Genomics to Clinical Information
-
-
-
39
-
-
85042040932
-
-
National Cancer Institute. Early onset malignancies initiative. National Cancer Institute
-
National Cancer Institute. Early onset malignancies initiative. National Cancer Institute https://www.cancer.gov/about-nci/organization/ccg/research/structural-genomics/early-onset-disparities (2017).
-
(2017)
-
-
-
40
-
-
84893379206
-
A systematic review of barriers and facilitators to minority research participation among African Americans, Latinos, Asian Americans, and Pacific Islanders
-
George, S., Duran, N. & Norris, K. A systematic review of barriers and facilitators to minority research participation among African Americans, Latinos, Asian Americans, and Pacific Islanders. Am. J. Public Health. 104, e16-e31 (2014).
-
(2014)
Am. J. Public Health.
, vol.104
, pp. e16-e31
-
-
George, S.1
Duran, N.2
Norris, K.3
-
41
-
-
33645814035
-
Effective recruitment and retention of minority research participants
-
Yancey, A. K., Ortega, A. N. & Kumanyika, S. K. Effective recruitment and retention of minority research participants. Annu. Rev. Public Health 27, 1-28 (2006).
-
(2006)
Annu. Rev. Public Health
, vol.27
, pp. 1-28
-
-
Yancey, A.K.1
Ortega, A.N.2
Kumanyika, S.K.3
-
42
-
-
83555173549
-
Differences between African American and White research volunteers in their attitudes, beliefs and knowledge regarding genetic testing for Alzheimer's disease
-
Akinleye, I. et al. Differences between African American and White research volunteers in their attitudes, beliefs and knowledge regarding genetic testing for Alzheimer's disease. J. Genet. Couns. 20, 650-659 (2011).
-
(2011)
J. Genet. Couns.
, vol.20
, pp. 650-659
-
-
Akinleye, I.1
-
43
-
-
33746512512
-
Principal components analysis corrects for stratification in genome-wide association studies
-
Price, A. L. et al. Principal components analysis corrects for stratification in genome-wide association studies. Nat. Genet. 38, 904-909 (2006).
-
(2006)
Nat. Genet.
, vol.38
, pp. 904-909
-
-
Price, A.L.1
-
44
-
-
77949772292
-
Gene-environment-wide association studies: Emerging approaches
-
Thomas, D. Gene-environment-wide association studies: emerging approaches. Nat. Rev. Genet. 11, 259-272 (2010).
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 259-272
-
-
Thomas, D.1
-
45
-
-
85041996474
-
-
National Institutes of Health. Diversity Matters. National Institutes of Health: Diversity in Extramural Programs
-
National Institutes of Health. Diversity Matters. National Institutes of Health: Diversity in Extramural Programs https://extramural-diversity.nih.gov/diversity-matters (2017).
-
(2017)
-
-
-
46
-
-
3142773390
-
Integrating ethics and science in the International HapMap Project
-
International HapMap Consortium
-
International HapMap Consortium. Integrating ethics and science in the International HapMap Project. Nat. Rev. Genet. 5, 467-475 (2004).
-
(2004)
Nat. Rev. Genet.
, vol.5
, pp. 467-475
-
-
-
48
-
-
84893616546
-
-
National Institutes of Health.. National Institutes of Health: Grants & Funding
-
National Institutes of Health. Genomic sequencing and newborn screening disorders (U19). National Institutes of Health: Grants & Funding https://grants.nih.gov/grants/guide/rfa-files/RFA-HD-13-010.html (2012).
-
(2012)
Genomic Sequencing and Newborn Screening Disorders (U19)
-
-
-
49
-
-
84906857914
-
-
National Institutes of Health.. National Institutes of Health: Grants & Funding
-
National Institutes of Health. Clinical sequencing exploratory research (UM1). National Institutes of Health: Grants & Funding https://grants.nih.gov/grants/guide/rfa-files/RFA-HG-12-009.html (2012).
-
(2012)
Clinical Sequencing Exploratory Research (UM1)
-
-
-
50
-
-
85042004372
-
-
National Institute of Minority Health and Health Disparities. Transdisciplinary Collaborative Centers for Health Disparities Research Program (TCC). National Institute of Minority Health and Health Disparities
-
National Institute of Minority Health and Health Disparities. Transdisciplinary Collaborative Centers for Health Disparities Research Program (TCC). National Institute of Minority Health and Health Disparities https://www.nimhd.nih.gov/programs/extramural/transdisciplinary-collab-centers.html#precision-research (2017).
-
(2017)
-
-
-
51
-
-
85019848351
-
Challenges and strategies for implementing genomic services in diverse settings: Experiences from the Implementing GeNomics in pracTicE (IGNITE) network
-
Sperber, N. R. et al. Challenges and strategies for implementing genomic services in diverse settings: experiences from the Implementing GeNomics In pracTicE (IGNITE) network. BMC Med. Genom. 10, 35 (2017).
-
(2017)
BMC Med. Genom.
, vol.10
, pp. 35
-
-
Sperber, N.R.1
-
52
-
-
85013911342
-
Race, genomics and chronic disease: What patients with African ancestry have to say
-
Horowitz, C. R. et al. Race, genomics and chronic disease: what patients with African ancestry have to say. J. Health Care Poor Underserved 28, 248-260 (2017).
-
(2017)
J. Health Care Poor Underserved
, vol.28
, pp. 248-260
-
-
Horowitz, C.R.1
-
53
-
-
85010635722
-
The study is open: Participants are now recruiting investigators
-
Terry, S. F. The study is open: Participants are now recruiting investigators. Sci. Transl Med. 9, eaaf1001 (2017).
-
(2017)
Sci. Transl Med.
, vol.9
, pp. eaaf1001
-
-
Terry, S.F.1
-
54
-
-
85042007838
-
-
National Human Genome Research Institute. Community Engagement in Genomics Working Group. National Human Genome Research Institute
-
National Human Genome Research Institute. Community Engagement in Genomics Working Group. National Human Genome Research Institute https://www.genome.gov/27568486/community-engagement-in-genomics-working-group/(2017).
-
(2017)
-
-
-
55
-
-
84996835614
-
The use of social media in recruitment for medical research studies: A scoping review
-
Topolovec-Vranic, J. & Natarajan, K. The use of social media in recruitment for medical research studies: a scoping review. J. Med. Internet Res. 18, e286 (2016).
-
(2016)
J. Med. Internet Res.
, vol.18
, pp. e286
-
-
Topolovec-Vranic, J.1
Natarajan, K.2
-
56
-
-
85042021247
-
-
National Center for Biotechnology Information. Database of Genotypes and Phenotypes (dbGaP). National Center for Biotechnology Information
-
National Center for Biotechnology Information. Database of Genotypes and Phenotypes (dbGaP). National Center for Biotechnology Information https://www.ncbi.nlm.nih.gov/gap (2017).
-
(2017)
-
-
-
57
-
-
85042039386
-
-
National Center for Biotechnology Information. ClinVar. National Center for Biotechnology Information
-
National Center for Biotechnology Information. ClinVar. National Center for Biotechnology Information https://www.ncbi.nlm.nih.gov/clinvar/(2017).
-
(2017)
-
-
-
58
-
-
84944345463
-
Building the foundation for genomics in precision medicine
-
Aronson, S. J. & Rehm, H. L. Building the foundation for genomics in precision medicine. Nature 526, 336-342 (2015).
-
(2015)
Nature
, vol.526
, pp. 336-342
-
-
Aronson, S.J.1
Rehm, H.L.2
-
59
-
-
84896278569
-
Facilitating health data sharing across diverse practices and communities
-
Lin, C. P. et al. Facilitating health data sharing across diverse practices and communities. AMIA Jt. Summits Transl Sci. Proc. 2010, 16-20 (2010).
-
(2010)
AMIA Jt. Summits Transl Sci. Proc.
, vol.2010
, pp. 16-20
-
-
Lin, C.P.1
-
60
-
-
84906544185
-
Exploring pathways to trust: A tribal perspective on data sharing
-
James, R. et al. Exploring pathways to trust: a tribal perspective on data sharing. Genet. Med. 16, 820-826 (2014).
-
(2014)
Genet. Med.
, vol.16
, pp. 820-826
-
-
James, R.1
-
61
-
-
84881421175
-
Biospecimen policy: Family matters
-
Hudson, K. L. & Collins, F. S. Biospecimen policy: family matters. Nature 500, 141-142 (2013).
-
(2013)
Nature
, vol.500
, pp. 141-142
-
-
Hudson, K.L.1
Collins, F.S.2
-
62
-
-
85042015190
-
-
The Genome Reference Consortium. The Genome Reference Consortium. National Center for Biotechnology Information
-
The Genome Reference Consortium. The Genome Reference Consortium. National Center for Biotechnology Information https://www.ncbi.nlm.nih.gov/grc (2017).
-
(2017)
-
-
-
63
-
-
85042027623
-
-
National Institutes of Health. High quality human and non-human primate genome sequences (U24). National Institutes of Health: Grants & Funding
-
National Institutes of Health. High quality human and non-human primate genome sequences (U24). National Institutes of Health: Grants & Funding https://grants.nih.gov/grants/guide/rfa-files/RFA-HG-15-027.html (2017).
-
(2017)
-
-
-
64
-
-
85042032739
-
-
NHLBI GO Exome Sequencing Project (ESP). Exome Variant Server. University of Washington
-
NHLBI GO Exome Sequencing Project (ESP). Exome Variant Server. University of Washington http://evs.gs.washington.edu/EVS/(2017).
-
(2017)
-
-
-
65
-
-
85011303767
-
The ExAC browser: Displaying reference data information from over 60 000 exomes
-
Karczewski, K. J. et al. The ExAC browser: displaying reference data information from over 60 000 exomes. Nucleic Acids Res. 45, D840-D845 (2017).
-
(2017)
Nucleic Acids Res.
, vol.45
, pp. D840-D845
-
-
Karczewski, K.J.1
-
66
-
-
85042013771
-
-
National Institutes of Health. NIH policy on reporting race and ethnicity data: subjects in clinical research. National Institutes of Health: Grants & Funding
-
National Institutes of Health. NIH policy on reporting race and ethnicity data: subjects in clinical research. National Institutes of Health: Grants & Funding https://grants.nih.gov/grants/guide/notice-files/NOT-OD-01-053.html (2001).
-
(2001)
-
-
-
67
-
-
84864417548
-
Fast and accurate genotype imputation in genome-wide association studies through pre-phasing
-
Howie, B., Fuchsberger, C., Stephens, M., Marchini, J. & Abecasis, G. R. Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. Nat. Genet. 44, 955-959 (2012).
-
(2012)
Nat. Genet.
, vol.44
, pp. 955-959
-
-
Howie, B.1
Fuchsberger, C.2
Stephens, M.3
Marchini, J.4
Abecasis, G.R.5
-
68
-
-
77953811255
-
New approaches to population stratification in genome-wide association studies
-
Price, A. L., Zaitlen, N. A., Reich, D. & Patterson, N. New approaches to population stratification in genome-wide association studies. Nat. Rev. Genet. 11, 459-463 (2010).
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 459-463
-
-
Price, A.L.1
Zaitlen, N.A.2
Reich, D.3
Patterson, N.4
-
69
-
-
79960566302
-
New approaches to disease mapping in admixed populations
-
Seldin, M. F., Pasaniuc, B. & Price, A. L. New approaches to disease mapping in admixed populations. Nat. Rev. Genet. 12, 523-528 (2011).
-
(2011)
Nat. Rev. Genet.
, vol.12
, pp. 523-528
-
-
Seldin, M.F.1
Pasaniuc, B.2
Price, A.L.3
-
70
-
-
79957616191
-
Mapping of disease-associated variants in admixed populations
-
Shriner, D., Adeyemo, A., Ramos, E., Chen, G. & Rotimi, C. N. Mapping of disease-associated variants in admixed populations. Genome Biol. 12, 223 (2011).
-
(2011)
Genome Biol.
, vol.12
, pp. 223
-
-
Shriner, D.1
Adeyemo, A.2
Ramos, E.3
Chen, G.4
Rotimi, C.N.5
-
71
-
-
84920807370
-
Trans-ethnic genome-wide association studies: Advantages and challenges of mapping in diverse populations
-
Li, Y. R. & Keating, B. J. Trans-ethnic genome-wide association studies: advantages and challenges of mapping in diverse populations. Genome Med. 6, 91 (2014).
-
(2014)
Genome Med.
, vol.6
, pp. 91
-
-
Li, Y.R.1
Keating, B.J.2
-
72
-
-
77951133654
-
Genome-wide association studies in diverse populations
-
Rosenberg, N. A. et al. Genome-wide association studies in diverse populations. Nat. Rev. Genet. 11, 356-366 (2010).
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 356-366
-
-
Rosenberg, N.A.1
-
73
-
-
84991577085
-
Guidelines for large-scale sequence-based complex trait association studies: Lessons learned from the NHLBI Exome Sequencing Project
-
Auer, P. L. et al. Guidelines for large-scale sequence-based complex trait association studies: lessons learned from the NHLBI Exome Sequencing Project. Am. J. Hum. Genet. 99, 791-801 (2016).
-
(2016)
Am. J. Hum. Genet.
, vol.99
, pp. 791-801
-
-
Auer, P.L.1
-
74
-
-
85019358299
-
Identification of unique venous thromboembolism-susceptibility variants in African-Americans
-
Heit, J. A. et al. Identification of unique venous thromboembolism-susceptibility variants in African-Americans. Thromb. Haemost. 117, 758-768 (2017).
-
(2017)
Thromb. Haemost.
, vol.117
, pp. 758-768
-
-
Heit, J.A.1
-
75
-
-
84899981111
-
Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa
-
Sangare, M. et al. Genetics of low spinal muscular atrophy carrier frequency in sub-Saharan Africa. Ann. Neurol. 75, 525-532 (2014).
-
(2014)
Ann. Neurol.
, vol.75
, pp. 525-532
-
-
Sangare, M.1
-
76
-
-
34249828965
-
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes
-
Steinthorsdottir, V. et al. A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. Nat. Genet. 39, 770-775 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 770-775
-
-
Steinthorsdottir, V.1
-
77
-
-
85017161994
-
Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci
-
Fernandez-Rhodes, L. et al. Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci. Hum. Genet. 136, 771-800 (2017).
-
(2017)
Hum. Genet.
, vol.136
, pp. 771-800
-
-
Fernandez-Rhodes, L.1
-
78
-
-
84928209346
-
Standards and guidelines for the interpretation of sequence variants: A joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
-
Richards, S. et al. Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet. Med. 17, 405-424 (2015).
-
(2015)
Genet. Med.
, vol.17
, pp. 405-424
-
-
Richards, S.1
-
79
-
-
84923872701
-
Actionable exomic incidental findings in 6503 participants: Challenges of variant classification
-
Amendola, L. M. et al. Actionable exomic incidental findings in 6503 participants: challenges of variant classification. Genome Res. 25, 305-315 (2015).
-
(2015)
Genome Res.
, vol.25
, pp. 305-315
-
-
Amendola, L.M.1
-
81
-
-
57549090341
-
Accounting for ancestry: Population substructure and genome-wide association studies
-
Tian, C., Gregersen, P. K. & Seldin, M. F. Accounting for ancestry: population substructure and genome-wide association studies. Hum. Mol. Genet. 17, R143-R150 (2008).
-
(2008)
Hum. Mol. Genet.
, vol.17
, pp. R143-R150
-
-
Tian, C.1
Gregersen, P.K.2
Seldin, M.F.3
-
82
-
-
84952908541
-
The IGNITE network: A model for genomic medicine implementation and research
-
Weitzel, K. W. et al. The IGNITE network: a model for genomic medicine implementation and research. BMC Med. Genom. 9, 1 (2016).
-
(2016)
BMC Med. Genom.
, vol.9
, pp. 1
-
-
Weitzel, K.W.1
-
83
-
-
85042002162
-
-
eMERGE Network. Collaborate. eMERGE Network
-
eMERGE Network. Collaborate. eMERGE Network https://emerge.mc.vanderbilt.edu/collaborate/(2017).
-
(2017)
-
-
-
84
-
-
0014067061
-
Glucose?6?Phosphate dehydrogenase deficiency Diagnosis, clinical and genetic implications
-
Beutler, E. Glucose?6?phosphate dehydrogenase deficiency. Diagnosis, clinical and genetic implications. Am. J. Clin. Pathol. 47, 303-311 (1967).
-
(1967)
Am. J. Clin. Pathol.
, vol.47
, pp. 303-311
-
-
Beutler, E.1
-
85
-
-
84869494804
-
HLA genotype and carbamazepine-induced cutaneous adverse drug reactions: A systematic review
-
Yip, V. L., Marson, A. G., Jorgensen, A. L., Pirmohamed, M. & Alfirevic, A. HLA genotype and carbamazepine-induced cutaneous adverse drug reactions: a systematic review. Clin. Pharmacol. Ther. 92, 757-765 (2012).
-
(2012)
Clin. Pharmacol. Ther.
, vol.92
, pp. 757-765
-
-
Yip, V.L.1
Marson, A.G.2
Jorgensen, A.L.3
Pirmohamed, M.4
Alfirevic, A.5
-
86
-
-
84997470869
-
Training the workforce for 21st?Century science
-
Berg, J., Hrabowski, F. & Zerhouni, E. Training the workforce for 21st?century science. JAMA 316, 1675-1676 (2016).
-
(2016)
JAMA
, vol.316
, pp. 1675-1676
-
-
Berg, J.1
Hrabowski, F.2
Zerhouni, E.3
-
87
-
-
84943338403
-
National Institutes of Health addresses the science of diversity
-
Valantine, H. A. & Collins, F. S. National Institutes of Health addresses the science of diversity. Proc. Natl Acad. Sci. USA 112, 12240-12242 (2015).
-
(2015)
Proc. Natl Acad. Sci. USA
, vol.112
, pp. 12240-12242
-
-
Valantine, H.A.1
Collins, F.S.2
-
88
-
-
84862227406
-
Diversity in the biomedical research workforce: Developing talent
-
McGee, R. Jr., Saran, S. & Krulwich, T. A. Diversity in the biomedical research workforce: developing talent. Mt. Sinai J. Med. 79, 397-411 (2012).
-
(2012)
Mt. Sinai J. Med.
, vol.79
, pp. 397-411
-
-
McGee, R.1
Saran, S.2
Krulwich, T.A.3
-
89
-
-
85042033258
-
-
National Institutes of Health. Notice of NIH's interest in diversity. National Institutes of Health: Grants & Funding
-
National Institutes of Health. Notice of NIH's interest in diversity. National Institutes of Health: Grants & Funding https://grants.nih.gov/grants/guide/notice-files/NOT-OD-15-053.html (2017).
-
(2017)
-
-
-
90
-
-
3242656174
-
-
National Science Foundation, National Center for Science and Engineering Statistics.. (National Science Foundation
-
National Science Foundation, National Center for Science and Engineering Statistics. Women, minorities, and persons with disabilities in science and engineering. (National Science Foundation, 2017).
-
(2017)
Women, Minorities, and Persons with Disabilities in Science and Engineering
-
-
-
91
-
-
80051871951
-
Race, ethnicity, and NIH research awards
-
Ginther, D. K. et al. Race, ethnicity, and NIH research awards. Science 333, 1015-1019 (2011).
-
(2011)
Science
, vol.333
, pp. 1015-1019
-
-
Ginther, D.K.1
-
92
-
-
85042002888
-
-
National Human Genome Research Institute. National Human Genome Research Institute
-
National Human Genome Research Institute. Plan for increasing the number of underrepresented minorities trained in genomics and ELSI research. National Human Genome Research Institute https://www.genome.gov/10001707/plan-for-increasing-the-number-of-underrepresented-minorities-trained-in-genomics-research/(2008).
-
(2008)
Plan for Increasing the Number of Underrepresented Minorities Trained in Genomics and ELSI Research
-
-
-
93
-
-
85041999801
-
-
National Human Genome Research Institute.. National Human Genome Research Institute
-
National Human Genome Research Institute. NHGRI's 11th annual meeting of DAP and T32 training programs. National Human Genome Research Institute https://www.genome.gov/pages/about/irminorities/eleventhannualdapmeeting.pdf (2014).
-
(2014)
NHGRI's 11th Annual Meeting of DAP and T32 Training Programs
-
-
-
94
-
-
85042004843
-
-
National Human Genome Research Institute.. National Human Genome Research Institute
-
National Human Genome Research Institute. Genomic medicine VIII: NHGRI's genomic medicine portfolio. Executive summary. National Human Genome Research Institute https://www.genome.gov/multimedia/slides/gm8/gm8executivesummary-gm8exec-odgisj.pdf (2015).
-
(2015)
Genomic Medicine VIII: NHGRI's Genomic Medicine Portfolio. Executive Summary
-
-
-
95
-
-
84923762812
-
A new initiative on precision medicine
-
Collins, F. S. & Varmus, H. A new initiative on precision medicine. N. Engl. J. Med. 372, 793-795 (2015).
-
(2015)
N. Engl. J. Med.
, vol.372
, pp. 793-795
-
-
Collins, F.S.1
Varmus, H.2
-
96
-
-
85042061053
-
-
International Committee of Medical Journal Editors. Recommendations for the conduct, reporting, editing, and publication of scholarly work in medical journals. International Committee of Medical Journal Editors
-
International Committee of Medical Journal Editors. Recommendations for the conduct, reporting, editing, and publication of scholarly work in medical journals. International Committee of Medical Journal Editors http://www.icmje.org/icmje-recommendations.pdf (2016).
-
(2016)
-
-
-
97
-
-
85042038531
-
-
Copenhagen
-
Bonham, V., Cornel, M., Kaariainen, H., Rotimi, C. & Robinson, H. M. in European Society of Human Genetics 2017 Conference (Copenhagen, 2017).
-
(2017)
European Society of Human Genetics 2017 Conference
-
-
Bonham, V.1
Cornel, M.2
Kaariainen, H.3
Rotimi, C.4
Robinson, H.M.5
-
100
-
-
84930433702
-
Global implementation of genomic medicine: We are not alone
-
Manolio, T. A. et al. Global implementation of genomic medicine: we are not alone. Sci. Transl Med. 7, 290ps13 (2015).
-
(2015)
Sci. Transl Med.
, vol.7
, pp. 290ps13
-
-
Manolio, T.A.1
-
101
-
-
84855843599
-
-
(eds Pagon, R. A. et al.) (University of Washington, Seattle
-
Cirino, A. L. & Ho, C. in GeneReviews (eds Pagon, R. A. et al.) (University of Washington, Seattle, 1993).
-
(1993)
GeneReviews
-
-
Cirino, A.L.1
Ho, C.2
-
102
-
-
84855843599
-
-
(eds Pagon, R. A. et al.) (University of Washington, Seattle
-
Petrucelli, N., Daly, M. B. & Pal, T. in GeneReviews (eds Pagon, R. A. et al.) (University of Washington, Seattle, 1993).
-
(1993)
GeneReviews
-
-
Petrucelli, N.1
Daly, M.B.2
Pal, T.3
-
103
-
-
84855843599
-
-
(eds Pagon, R. A. et al.) (University of Washington, Seattle
-
Bender, M. A. & Douthitt Seibel, G. in GeneReviews (eds Pagon, R. A. et al.) (University of Washington, Seattle, 1993).
-
(1993)
GeneReviews
-
-
Bender, M.A.1
Douthitt Seibel, G.2
-
105
-
-
85011835129
-
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): A policy statement of the American College of Medical Genetics and Genomics
-
Kalia, S. S. et al. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics. Genet. Med. 19, 249-255 (2017).
-
(2017)
Genet. Med.
, vol.19
, pp. 249-255
-
-
Kalia, S.S.1
-
106
-
-
84979523711
-
Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine
-
Petrovski, S. & Goldstein, D. B. Unequal representation of genetic variation across ancestry groups creates healthcare inequality in the application of precision medicine. Genome Biol. 17, 157 (2016).
-
(2016)
Genome Biol.
, vol.17
, pp. 157
-
-
Petrovski, S.1
Goldstein, D.B.2
-
107
-
-
0032429154
-
DNA polymorphism discovery resource for research on human genetic variation
-
Collins, F. S., Brooks, L. D. & Chakravarti, A. A. DNA polymorphism discovery resource for research on human genetic variation. Genome Res. 8, 1229-1231 (1998).
-
(1998)
Genome Res.
, vol.8
, pp. 1229-1231
-
-
Collins, F.S.1
Brooks, L.D.2
Chakravarti, A.A.3
-
108
-
-
84880059657
-
The Electronic Medical Records and Genomics (eMERGE) Network: Past, present, and future
-
Gottesman, O. et al. The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future. Genet. Med. 15, 761-771 (2013).
-
(2013)
Genet. Med.
, vol.15
, pp. 761-771
-
-
Gottesman, O.1
-
109
-
-
84860874813
-
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network
-
Crosslin, D. R. et al. Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network. Hum. Genet. 131, 639-652 (2012).
-
(2012)
Hum. Genet.
, vol.131
, pp. 639-652
-
-
Crosslin, D.R.1
|