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1
Variant PADI3 in Central Centrifugal Cicatricial Alopecia
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Variant PADI3 in Central Centrifugal Cicatricial Alopecia

The New England journal of medicine, 2019-02, Vol.380 (9), p.833-841 [Peer Reviewed Journal]

Copyright © 2019 Massachusetts Medical Society. All rights reserved. ;Copyright © 2019 Massachusetts Medical Society. ;Distributed under a Creative Commons Attribution 4.0 International License ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1816614 ;PMID: 30763140

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2
Genetic Misdiagnoses and the Potential for Health Disparities
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Genetic Misdiagnoses and the Potential for Health Disparities

The New England journal of medicine, 2016-08, Vol.375 (7), p.655-665 [Peer Reviewed Journal]

Copyright © 2016 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMsa1507092 ;PMID: 27532831

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3
Cardiovascular Health in African Americans: A Scientific Statement From the American Heart Association
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Cardiovascular Health in African Americans: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2017-11, Vol.136 (21), p.e393-e423 [Peer Reviewed Journal]

2017 by the American College of Cardiology Foundation and the American Heart Association, Inc. ;2017 American Heart Association, Inc. ;ISSN: 0009-7322 ;EISSN: 1524-4539 ;DOI: 10.1161/CIR.0000000000000534 ;PMID: 29061565

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4
Beyond 2/3 and 1/3: The Complex Signatures of Sex-Biased Admixture on the X Chromosome
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Beyond 2/3 and 1/3: The Complex Signatures of Sex-Biased Admixture on the X Chromosome

Genetics (Austin), 2015-09, Vol.201 (1), p.263-279 [Peer Reviewed Journal]

Copyright © 2015 by the Genetics Society of America. ;Copyright Genetics Society of America Sep 2015 ;Copyright © 2015 by the Genetics Society of America 2015 ;ISSN: 1943-2631 ;ISSN: 0016-6731 ;EISSN: 1943-2631 ;DOI: 10.1534/genetics.115.178509 ;PMID: 26209245 ;CODEN: GENTAE

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5
Clinically Actionable Genotypes Among 10,000 Patients With Preemptive Pharmacogenomic Testing
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Clinically Actionable Genotypes Among 10,000 Patients With Preemptive Pharmacogenomic Testing

Clinical pharmacology and therapeutics, 2014-04, Vol.95 (4), p.423-431 [Peer Reviewed Journal]

2014 American Society for Clinical Pharmacology and Therapeutics ;2015 INIST-CNRS ;ISSN: 0009-9236 ;EISSN: 1532-6535 ;DOI: 10.1038/clpt.2013.229 ;PMID: 24253661 ;CODEN: CLPTAT

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6
Integrated Analysis of Genetic Ancestry and Genomic Alterations across Cancers
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Article
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Integrated Analysis of Genetic Ancestry and Genomic Alterations across Cancers

Cancer cell, 2018-10, Vol.34 (4), p.549-560.e9 [Peer Reviewed Journal]

2018 Elsevier Inc. ;Copyright © 2018 Elsevier Inc. All rights reserved. ;ISSN: 1535-6108 ;EISSN: 1878-3686 ;DOI: 10.1016/j.ccell.2018.08.019 ;PMID: 30300578

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7
Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
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Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study

Human molecular genetics, 2011-06, Vol.20 (11), p.2273-2284 [Peer Reviewed Journal]

2015 INIST-CNRS ;The Author 2011. Published by Oxford University Press. 2011 ;ISSN: 0964-6906 ;ISSN: 1460-2083 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddr092 ;PMID: 21378095

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8
Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism
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Article
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Apolipoprotein(a) Genetic Sequence Variants Associated With Systemic Atherosclerosis and Coronary Atherosclerotic Burden But Not With Venous Thromboembolism

Journal of the American College of Cardiology, 2012-08, Vol.60 (8), p.722-729 [Peer Reviewed Journal]

American College of Cardiology Foundation ;2012 American College of Cardiology Foundation ;2015 INIST-CNRS ;Copyright © 2012 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved. ;Copyright Elsevier Limited Aug 21, 2012 ;ISSN: 0735-1097 ;ISSN: 1558-3597 ;EISSN: 1558-3597 ;DOI: 10.1016/j.jacc.2012.01.078 ;PMID: 22898070 ;CODEN: JACCDI

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9
Racial Differences in Genomic Profiling of Prostate Cancer
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Article
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Racial Differences in Genomic Profiling of Prostate Cancer

The New England journal of medicine, 2020-09, Vol.383 (11), p.1083-1085 [Peer Reviewed Journal]

Copyright © 2020 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMc2000069 ;PMID: 32905685

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10
Vitamin D–Binding Protein and Vitamin D Status of Black Americans and White Americans
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Article
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Vitamin D–Binding Protein and Vitamin D Status of Black Americans and White Americans

The New England journal of medicine, 2013-11, Vol.369 (21), p.1991-2000 [Peer Reviewed Journal]

Copyright © 2013 Massachusetts Medical Society. All rights reserved. ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1306357 ;PMID: 24256378

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11
Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
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Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Nature genetics, 2017-06, Vol.49 (6), p.946-952 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Jun 2017 ;ISSN: 1061-4036 ;ISSN: 1546-1718 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3843 ;PMID: 28416818

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12
Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci
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Epigenome-wide association study (EWAS) of BMI, BMI change and waist circumference in African American adults identifies multiple replicated loci

Human molecular genetics, 2015-08, Vol.24 (15), p.4464-4479 [Peer Reviewed Journal]

The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com. ;The Author 2015. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com 2015 ;ISSN: 0964-6906 ;ISSN: 1460-2083 ;EISSN: 1460-2083 ;DOI: 10.1093/hmg/ddv161 ;PMID: 25935004

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13
DNA methylation contributes to natural human variation
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DNA methylation contributes to natural human variation

Genome research, 2013-09, Vol.23 (9), p.1363-1372 [Peer Reviewed Journal]

info:eu-repo/semantics/openAccess This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported), as described at http://creativecommons.org/licenses/by-nc/3.0/. http://creativecommons.org/licenses/by-nc/3.0/ ;2013 ;ISSN: 1088-9051 ;EISSN: 1549-5469 ;DOI: 10.1101/gr.154187.112 ;PMID: 23908385

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14
Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1
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Innate immunity pathways regulate the nephropathy gene Apolipoprotein L1

Kidney international, 2015-02, Vol.87 (2), p.332-342 [Peer Reviewed Journal]

2015 International Society of Nephrology ;Copyright Nature Publishing Group Feb 2015 ;ISSN: 0085-2538 ;EISSN: 1523-1755 ;DOI: 10.1038/ki.2014.270 ;PMID: 25100047

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15
End‐Stage Renal Disease in African Americans With Lupus Nephritis Is Associated With APOL1
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End‐Stage Renal Disease in African Americans With Lupus Nephritis Is Associated With APOL1

Arthritis & rheumatology (Hoboken, N.J.), 2014-02, Vol.66 (2), p.390-396 [Peer Reviewed Journal]

Copyright © 2014 by the American College of Rheumatology ;Copyright © 2014 by the American College of Rheumatology. ;2014, American College of Rheumatology 2014 ;ISSN: 2326-5191 ;EISSN: 2326-5205 ;DOI: 10.1002/art.38220 ;PMID: 24504811

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16
Genetic Ancestry to Improve Precision of Race/Ethnicity-based Lung Function Equations in Children
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Article
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Genetic Ancestry to Improve Precision of Race/Ethnicity-based Lung Function Equations in Children

American journal of respiratory and critical care medicine, 2022-03, Vol.205 (6), p.725-727 [Peer Reviewed Journal]

Copyright American Thoracic Society Mar 15, 2022 ;ISSN: 1073-449X ;EISSN: 1535-4970 ;DOI: 10.1164/rccm.202109-2088LE ;PMID: 35085059

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17
Population genetics models of local ancestry
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Article
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Population genetics models of local ancestry

Genetics (Austin), 2012-06, Vol.191 (2), p.607-619 [Peer Reviewed Journal]

Copyright Genetics Society of America Jun 2012 ;Copyright © 2012 by the Genetics Society of America 2012 ;ISSN: 1943-2631 ;ISSN: 0016-6731 ;EISSN: 1943-2631 ;DOI: 10.1534/genetics.112.139808 ;PMID: 22491189 ;CODEN: GENTAE

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18
APOL1 Risk Variants, Race, and Progression of Chronic Kidney Disease
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Article
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APOL1 Risk Variants, Race, and Progression of Chronic Kidney Disease

The New England journal of medicine, 2013-12, Vol.369 (23), p.2183-2196 [Peer Reviewed Journal]

Copyright © 2013 Massachusetts Medical Society. All rights reserved. ;2014 INIST-CNRS ;Copyright © 2013 Massachusetts Medical Society. 2013 ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMoa1310345 ;PMID: 24206458 ;CODEN: NEJMAG

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19
A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseases
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Article
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A missense variant in NCF1 is associated with susceptibility to multiple autoimmune diseases

Nature genetics, 2017-03, Vol.49 (3), p.433-437 [Peer Reviewed Journal]

COPYRIGHT 2017 Nature Publishing Group ;COPYRIGHT 2017 Nature Publishing Group ;Copyright Nature Publishing Group Mar 2017 ;ISSN: 1061-4036 ;EISSN: 1546-1718 ;DOI: 10.1038/ng.3782 ;PMID: 28135245

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20
Embracing Genetic Diversity to Improve Black Health
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Embracing Genetic Diversity to Improve Black Health

The New England journal of medicine, 2021-03, Vol.384 (12), p.1163-1167 [Peer Reviewed Journal]

Copyright © 2021 Massachusetts Medical Society. All rights reserved. ;COPYRIGHT 2021 Massachusetts Medical Society ;ISSN: 0028-4793 ;EISSN: 1533-4406 ;DOI: 10.1056/NEJMms2031080 ;PMID: 33567186

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