Gail P. Jarvik

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 1%percentile

11.0Author DataRank

Indexed papers

4in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 4 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x

Top 2%

8.6DataRank

Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Papers

Driven by 89 papers — median percentile 88. Top paper: “Genomic data in the All of Us Research Program”.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x

Top 2%

8.6DataRank

Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

Nature Medicine(2022)10.1038/s41591-022-01891-3

N/A

6.8DataRank · unranked

363 citations

Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni, Shining Ma +78 more

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

Human Genetics(2014)10.1007/s00439-013-1355-7

N/A

5.1DataRank · unranked

148 citations

Joshua C. Denny, Keyue Ding, Hayan Jouni, David R. Crosslin, Mariza de Andrade +15 more

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Nature Medicine(2024)10.1038/s41591-024-02796-z

N/A

4.8DataRank · unranked

196 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin +73 more

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006

N/A

2.6DataRank · unranked

121 citations

Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton +95 more

The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-023-05708-y

Top 12%

1.7DataRank

Top 12%52 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +95 more

Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.021

N/A

1.3DataRank · unranked

70 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian Wang, Margaret Sunitha Selvaraj +95 more

Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study

Circulation(2021)10.1161/circulationaha.121.055562

N/A

1.2DataRank · unranked

49 citations

Giovanni Davogustto, Christian M. Shaffer, Carlos G. Vanoye, Reshma R. Desai, Eric Farber‐Eger +46 more

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

Nature Communications(2021)10.1038/s41467-021-22339-1

N/A

1.1DataRank · unranked

51 citations

Akhil Pampana, Sarah E. Graham, Sanni Ruotsalainen, James A. Perry, Paul S. de Vries +95 more

GWAS of multiple neuropathology endophenotypes identifies new risk loci and provides insights into the genetic risk of dementia

Nature Genetics(2024)10.1038/s41588-024-01939-9

N/A

1.1DataRank · unranked

66 citations

Yuriko Katsumata, Erin L. Abner, Khine Zin Aung, Steven A. Claas, Qi Qiao +91 more

Harmonizing variant classification for return of results in the All of Us Research Program

Human Mutation(2021)10.1002/humu.24317

Top 27%

0.738DataRank

Top 27%17 citations

Christina Austin‐Tse, Serra Kim, Matthew S. Lebo, Annette Leon, David R. Murdock +8 more

Diabetes Impairs Cellular Cholesterol Efflux From ABCA1 to Small HDL Particles

Circulation Research(2020)10.1161/circresaha.120.317178

N/A

0.648DataRank · unranked

74 citations

Graziella E. Ronsein, Chongren Tang, Gail P. Jarvik, W. Sean Davidson, Vishal Kothari +5 more

A large-scale multi-ethnic genome-wide association study of coronary artery disease

Research Square(2021)10.21203/rs.3.rs-275591/v1

N/A

0.561DataRank · unranked

11 citations

Catherine Tcheandjieu, Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni +77 more

Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.22.423783

N/A

0.534DataRank · unranked

11 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian X. Wang, Margaret Sunitha Selvaraj +95 more

Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates

Genetics in Medicine(2021)10.1016/j.gim.2021.10.010

N/A

0.494DataRank · unranked

26 citations

Wanfeng Yu, Andrea M. Oza, Megan Hawley, Prathik K. Vijay Kumar, Christopher Koch +12 more

Risk factors affecting polygenic score performance across diverse cohorts

eLife(2023)10.7554/elife.88149

N/A

0.312DataRank · unranked

7 citations

Scott Dudek, Krzysztof Kiryluk, Theresa L. Walunas, Iftikhar J. Kullo, Wei‐Qi Wei +16 more

Clinical associations with a polygenic predisposition to benign lower white blood cell counts

Nature Communications(2024)10.1038/s41467-024-47804-5

N/A

0.312DataRank · unranked

7 citations

John P. Shelley, Alyson L. Dickson, Jacy Zanussi, Laura L. Daniel, Neil S. Zheng +23 more

Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

Scientific Reports(2023)10.1038/s41598-023-45649-4

N/A

0.281DataRank · unranked

3 citations

Taryn O. Hall, Dana C. Crawford, Robb Rowley, Benjamin A. Satterfield, Rongling Li +21 more

Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100010

N/A

0.269DataRank · unranked

5 citations

Xiaoliang Wang, Pierre Fontanillas, Esther Kim, Sirisak Chanprasert, Allan Gordon +55 more

Dominant‐negative variant in SLC1A4 causes an autosomal dominant epilepsy syndrome

Annals of Clinical and Translational Neurology(2023)10.1002/acn3.51786

N/A

0.241DataRank · unranked

4 citations

Ghayda Mirzaa, Elizabeth Blue, Giuseppe Albano, Danny E. Miller, Aimee Allworth +28 more

Genome-wide polygenic score with APOL1 risk genotypes predicts chronic kidney disease across major continental ancestries

medRxiv(2021)10.1101/2021.10.25.21265398

N/A

0.218DataRank · unranked

2 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +33 more

Multiple polygenic score approach in colorectal cancer risk prediction

Scientific Reports(2025)10.1038/s41598-025-21956-w

N/A

0.104DataRank · unranked

1 citations

Minta Thomas, Elisabeth A. Rosenthal, Amanda I. Phipps, Lori C. Sakoda, Franzel J. B. van Duijnhoven +39 more

The All of Us Research Program: Data quality, utility, and diversity

Patterns(2022)10.1016/j.patter.2022.100570

N/A

0DataRank · unranked

337 citations

Lina Sulieman, David J. Schlueter, Alese E. Halvorson, Jun Qian, Francis Ratsimbazafy +81 more

Genome-wide polygenic score to predict chronic kidney disease across ancestries

Nature Medicine(2022)10.1038/s41591-022-01869-1

N/A

0DataRank · unranked

162 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +34 more

Multiancestral polygenic risk score for pediatric asthma

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.03.035

N/A

0DataRank · unranked

50 citations

Michael Lape, Edyta Małolepsza, Stanley B. DeVore, Matthew T. Weirauch, Ozan Dikilitas +19 more

Manifestations of Alzheimer’s disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90

Scientific Reports(2022)10.1038/s41598-022-09825-2

N/A

0DataRank · unranked

28 citations

John C. Earls, Andrew T. Magis, Sergey A. Kornilov, Jennifer C. Lovejoy, Cory C. Funk +94 more

An accessible, relational, inclusive, and actionable (ARIA) model of genetic counseling compared with usual care: Results of a randomized controlled trial

Genetics in Medicine(2022)10.1016/j.gim.2022.07.025

N/A

0DataRank · unranked

13 citations

Michael C. Leo, Leslie Riddle, Cláudia Guerra, Laura M. Amendola, Marian J. Gilmore +16 more

Uterine fibroid polygenic risk score (PRS) associates and predicts risk for uterine fibroid

Human Genetics(2022)10.1007/s00439-022-02442-z

N/A

0DataRank · unranked

14 citations

Jacklyn N. Hellwege, Yanfei Zhang, Eric S. Torstenson, Gail P. Jarvik, Ozan Dikilitas +10 more

Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100120

N/A

0DataRank · unranked

12 citations

Laura M. Amendola, Tia L. Kauffman, Kathleen F. Mittendorf, Jeannette T. Bensen, Flavia Chen +15 more

Precision medicine for developmental and epileptic encephalopathies in Africa—strategies for a resource-limited setting

Genetics in Medicine(2022)10.1016/j.gim.2022.11.002

N/A

0DataRank · unranked

12 citations

Nicki Tiffin, Gillian Riordan, Marie Wessels, Richard J. Burman, Miriam C. Aziz +49 more

Risk‐reducing surgery in unaffected individuals receiving cancer genetic testing in an integrated health care system

Cancer(2022)10.1002/cncr.34349

N/A

0DataRank · unranked

9 citations

Boya Guo, Kathleen F. Mittendorf, Heather Spencer Feigelson, Marian J. Gilmore, Gail P. Jarvik +10 more

Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access

Genetics in Medicine(2022)10.1016/j.gim.2022.02.006

N/A

0DataRank · unranked

11 citations

Elizabeth Shuster, Michael C. Leo, Michael O. Dorschner, Bradley A. Rolf, Brian H. Shirts +73 more

A research agenda to support the development and implementation of genomics-based clinical informatics tools and resources

Journal of the American Medical Informatics Association(2022)10.1093/jamia/ocac057

N/A

0DataRank · unranked

9 citations

Laura Findley, Madison P. Goldrich, Tejinder Rakhra-Burris, Ana Stevens, Pamela A. Williams +34 more

Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities

PLoS ONE(2022)10.1371/journal.pone.0268725

N/A

0DataRank · unranked

4 citations

Elizaveta E. Elgaeva, Ian B. Stanaway, Gail P. Jarvik, Bahram Namjou, Wei‐Qi Wei +5 more

Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index

medRxiv(2022)10.1101/2022.05.27.22275647

N/A

0DataRank · unranked

5 citations

Brenda Xiao, Ozan Dikilitas, Robert R. Freimuth, Marguerite R. Irvin, Gail P. Jarvik +14 more

LATE-NC risk alleles (in TMEM106B, GRN, and ABCC9 genes) among persons with African ancestry

Journal of Neuropathology & Experimental Neurology(2023)10.1093/jnen/nlad059

N/A

0DataRank · unranked

18 citations

David W. Fardo, Lincoln M. P. Shade, James D. Bowen, Paul K. Crane, Gail P. Jarvik +94 more

Genome-wide Association Study for AKI

Kidney360(2023)10.34067/kid.0000000000000175

N/A

0DataRank · unranked

15 citations

Ian B. Stanaway, Melody R. Palmer, Rajasree Menon, Jennifer A. Schaub, Steven Menez +20 more

Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population

Genetics in Medicine(2023)10.1016/j.gim.2023.100923

N/A

0DataRank · unranked

15 citations

Leslie Riddle, Galen Joseph, Laura M. Amendola, Marian J. Gilmore, Jamilyn M. Zepp +73 more

Genetics of varicose veins reveals polygenic architecture and genetic overlap with arterial and venous disease

Nature Cardiovascular Research(2023)10.1038/s44161-022-00196-5

N/A

0DataRank · unranked

14 citations

Jennifer E. Huffman, Anurag Verma, Kyle A. Sullivan, Alexis Rodriguez, David Kainer +17 more

Longitudinal adherence to breast cancer surveillance following cancer genetic testing in an integrated health care system

Breast Cancer Research and Treatment(2023)10.1007/s10549-023-07007-w

N/A

0DataRank · unranked

7 citations

Boya Guo, Karen J. Wernli, Kathleen F. Mittendorf, Heather Spencer Feigelson, Marian J. Gilmore +13 more

Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience

UNC Libraries(2023)10.17615/wbfb-8h23

N/A

0DataRank · unranked

2 citations

P. Murali, Fangjing Chen, R. Green, Mark Kvale, David R. Crosslin +15 more

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535

N/A

0DataRank · unranked

7 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more

Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.26.559521

N/A

0DataRank · unranked

7 citations

Jonas Korlach, Kiara C. Eldred, Elliott Swanson, Jason G. Underwood, Yong-Han Hank Cheng +31 more

Genetic Predictors of Blood Pressure Traits are Associated with Preeclampsia

medRxiv(2023)10.1101/2023.02.09.23285734

N/A

0DataRank · unranked

0 citations

Jacklyn N. Hellwege, Joseph H. Breeyear, Brenda Xiao, Gail P. Jarvik, Ian B. Stanaway +10 more

Clinical consequences of a polygenic predisposition to benign lower white blood cell counts

medRxiv(2023)10.1101/2023.08.20.23294331

N/A

0DataRank · unranked

0 citations

John P. Shelley, Alyson L. Dickson, Jacy Zanussi, Laura L. Daniel, Neil S. Zheng +23 more

Amyloid-β predominant Alzheimer’s disease neuropathologic change

Brain(2024)10.1093/brain/awae325

N/A

0DataRank · unranked

15 citations

Yuriko Katsumata, Xian Wu, Khine Zin Aung, David W. Fardo, Shelley L. Forrest +95 more

CFAP47 is Implicated in X-Linked Polycystic Kidney Disease

Kidney International Reports(2024)10.1016/j.ekir.2024.09.013

N/A

0DataRank · unranked

4 citations

Takuya Fujimaru, Chunyu Liu, Karynne Patterson, Kouhei Yamamoto, Takefumi Suzuki +63 more

Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts

Rare(2024)10.1016/j.rare.2024.100040

N/A

0DataRank · unranked

3 citations

Samuel J. Huang, Alyna Khan, Katie Golden‐Grant, Brenna Boyd, Elisabeth A. Rosenthal +37 more

Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.07.008

N/A

0DataRank · unranked

3 citations

Eunjin Ryu, Benjamin Steger, Abhijit Dixit, Yoshihiko Saito, Juyeong Yoo +36 more

Genetic predictors of blood pressure traits are associated with preeclampsia

Scientific Reports(2024)10.1038/s41598-024-68469-6

N/A

0DataRank · unranked

2 citations

Jacklyn N. Hellwege, Joseph H. Breeyear, Brenda Xiao, Gail P. Jarvik, Ian B. Stanaway +10 more

Comparing Ancestry Standardization Approaches for a Transancestry Colorectal Cancer Polygenic Risk Score

Genetic Epidemiology(2024)10.1002/gepi.22590

N/A

0DataRank · unranked

2 citations

Li Hsu, Minta Thomas, Ulrike Peters, Christopher Kachulis, Karynne Patterson +2 more

Expanding the genetic landscape of endometriosis: Integrative -omics analyses implicate key genes and pathways in a multi-ancestry study of over one million women

medRxiv(2024)10.1101/2024.11.26.24316723

N/A

0DataRank · unranked

7 citations

Jagyashila Das, Lannawill Caruth, Ananya Rajagopalan, Alexis T. Akerele, Ben Brumpton +33 more

Multi-ancestry GWAS of severe pregnancy nausea and vomiting identifies risk loci associated with appetite, insulin signaling, and brain plasticity

medRxiv(2024)10.1101/2024.11.19.24317559

N/A

0DataRank · unranked

3 citations

Xinran Wang, Julia Zöllner, Natàlia Pujol‐Gualdo, Triin Laisk, Sarah Finer +24 more

Enhancing Genetic Association Power in Endometriosis through Unsupervised Clustering of Clinical Subtypes Identified from Electronic Health Records

medRxiv(2024)10.1101/2024.04.22.24306092

N/A

0DataRank · unranked

2 citations

Leigh Ann Humphrey, Margaret Rush, Meredith Pollie, Yuan Luo, Chunhua Weng +12 more

Enhancing genetic association power in endometriosis through unsupervised clustering of clinical subtypes identified from electronic health records

Research Square(2024)10.21203/rs.3.rs-5004325/v1

N/A

0DataRank · unranked

1 citations

Lindsay Guare, Leigh Ann Humphrey, Margaret Rush, Meredith Pollie, James Jaworski +13 more

Multi-ancestry genome-wide association study of severe pregnancy nausea and vomiting identifies risk loci associated with appetite, insulin signaling, and brain plasticity

Research Square(2024)10.21203/rs.3.rs-5487737/v1

N/A

0DataRank · unranked

1 citations

Xinran Wang, Julia Zöllner, Natàlia Pujol‐Gualdo, Triin Laisk, Sarah Finer +22 more

Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-024-06408-x

N/A

0DataRank · unranked

0 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +93 more

Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.002

N/A

0DataRank · unranked

175 citations

Daniel J. Schaid, Matthew Kosel, Robert J. Carroll, Christopher G. Chute, Joshua C. Denny +17 more

Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants

Science(2025)10.1126/science.adp4753

N/A

0DataRank · unranked

48 citations

Amin Abedini, Eunji Ha, Ziyuan Ma, Xin Sheng, Bernhard Dumoulin +94 more

Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition

Nature Genetics(2025)10.1038/s41588-024-02067-0

N/A

0DataRank · unranked

34 citations

Jonas Korlach, Kiara C. Eldred, Elliott Swanson, Jason G. Underwood, Stephanie C. Bohaczuk +33 more

Transformer patient embedding using electronic health records enables patient stratification and progression analysis

npj Digital Medicine(2025)10.1038/s41746-025-01872-z

N/A

0DataRank · unranked

10 citations

Monika E. Grabowska, Iftikhar J. Kullo, Yuan Luo, Jordan W. Smoller, Theresa L. Walunas +5 more

Genomic sequencing in diverse and underserved pediatric populations: Parent perspectives on understanding, uncertainty, psychosocial impact, and personal utility of results

Genetics in Medicine(2025)10.1016/j.gim.2025.101363

N/A

0DataRank · unranked

3 citations

Sara Ackerman, Kyle B. Brothers, Kelly M. East, Ann Katherine M. Foreman, Lucia A. Hindorff +14 more

Polygenic risk scores in the clinic: Health-system leaders and primary care providers weigh in

Genetics in Medicine(2025)10.1016/j.gim.2025.101575

N/A

0DataRank · unranked

2 citations

Stephanie M. Fullerton, Betty Cohn, David R. Crosslin, Gail P. Jarvik, Susan Brown Trinidad

Association of HFE genotypes with hemochromatosis-related phenotypes in the All of Us research program

Genetics in Medicine Open(2025)10.1016/j.gimo.2024.101959

N/A

0DataRank · unranked

1 citations

Ramal Moonesinghe, Lu Shi, Paul C. Adams, Gail P. Jarvik, Kris V. Kowdley +5 more

Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions

medRxiv(2025)10.1101/2025.11.07.25339764

N/A

0DataRank · unranked

3 citations

Adriana E. Sedeño-Cortés, Jane Ranchalis, Katherine M. Munson, Mitchell R. Vollger, Elsa Balton +15 more

Risk factors affecting polygenic score performance across diverse cohorts

eLife(2025)10.7554/elife.88149.3

N/A

0DataRank · unranked

0 citations

Scott Dudek, Krzysztof Kiryluk, Theresa L. Walunas, Iftikhar Kullo, Wei‐Qi Wei +16 more

Expanding the genetic landscape of endometriosis: Integrative -omics analyses implicate key genes and pathways in a multi-ancestry study of over one million women

Research Square(2025)10.21203/rs.3.rs-8116602/v1

N/A

0DataRank · unranked

0 citations

Lindsay Guare, Jagyashila Das, Lannawill Caruth, Ananya Rajagopalan, Alexis T. Akerele +31 more

Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain

UNC Libraries(2024)10.17615/36rr-ma25

N/A

0DataRank · unranked

0 citations

Blair Smith, Magnus K. Karlsson, Michelle S. Yau, Frances M. K. Williams, Traci M. Bartz +32 more

Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.09.011

N/A

0DataRank · unranked

112 citations

Kathleen Muenzen, Leslie G. Biesecker, Kevin M. Bowling, Gregory M. Cooper, Michael O. Dorschner +25 more

A genome-wide association study of polycystic ovary syndrome identified from electronic health records

American Journal of Obstetrics and Gynecology(2020)10.1016/j.ajog.2020.04.004

N/A

0DataRank · unranked

104 citations

Kevin Ho, Jacob M. Keaton, Dustin N. Hartzel, Felix R. Day, Anne E. Justice +15 more

A Polygenic and Phenotypic Risk Prediction for Polycystic Ovary Syndrome Evaluated by Phenome-Wide Association Studies

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgz326

N/A

0DataRank · unranked

64 citations

Ky’Era V. Actkins, Jennifer A. Pacheco, Anna O. Basile, Robert J. Carroll, David R. Crosslin +66 more

Development and early implementation of an Accessible, Relational, Inclusive and Actionable approach to genetic counseling: The ARIA model

Patient Education and Counseling(2020)10.1016/j.pec.2020.12.017

N/A

0DataRank · unranked

23 citations

Laura M. Amendola, Marian J. Gilmore, Cláudia Guerra, Barbara B. Biesecker, Tia L. Kauffman +9 more

The polygenic architecture of left ventricular mass mirrors the clinical epidemiology

Scientific Reports(2020)10.1038/s41598-020-64525-z

N/A

0DataRank · unranked

18 citations

Rebecca T. Levinson, Eric Farber‐Eger, Todd L. Edwards, Jacklyn N. Hellwege, Adriana M. Hung +20 more

Pleiotropy in the Genetic Predisposition to Rheumatoid Arthritis: A Phenome‐Wide Association Study and Inverse Variance–Weighted Meta‐Analysis

Arthritis & Rheumatology(2020)10.1002/art.41291

N/A

0DataRank · unranked

17 citations

Mingjian Shi, Qiping Feng, Cecilia P. Chung, Ge Liu, Nancy J. Cox +13 more

Differences in atheroma between Caucasian and Asian subjects with anterior stroke: A vessel wall MRI study

Stroke and Vascular Neurology(2020)10.1136/svn-2020-000370

N/A

0DataRank · unranked

14 citations

Mi Shen, Binbin Sui, Peiyi Gao, Dong Zhang, Jie Sun +9 more

Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study

PLoS Genetics(2020)10.1371/journal.pgen.1008684

N/A

0DataRank · unranked

33 citations

Mariaelisa Graff, Jeffrey Haessler, Steven Buyske, Stephanie A. Bien, Ran Tao +49 more

Loci identified by a genome‐wide association study of carotid artery stenosis in the eMERGE network

Genetic Epidemiology(2020)10.1002/gepi.22360

N/A

0DataRank · unranked

10 citations

Daniel Seung Kim, David R. Crosslin, Ian B. Stanaway, Elisabeth A. Rosenthal, David Carrell +19 more

Generalizability of Polygenic Risk Scores for Breast Cancer in the Multiethnic eMERGE Study

medRxiv(2020)10.1101/2020.08.17.20176685

N/A

0DataRank · unranked

0 citations

Nur Zeinomar, Wendy K. Chung, Krzysztof Kiryluk, Ali G. Ghravi, George Hripcsak +17 more

A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record

UNC Libraries(2020)10.17615/4zec-ff92

N/A

0DataRank · unranked

0 citations

Matthew S. Lebo, Samuel Aronson, Laura M. Amendola, Levi A. Garraway, Gail P. Jarvik +10 more

Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between

UNC Libraries(2020)10.17615/rpzn-a165

N/A

0DataRank · unranked

0 citations

Gail P. Jarvik, Nanibaa’ A. Garrison, Wylie Burke, Jonathan S. Berg, John F. Connolly +27 more

ClinGen Pathogenicity Calculator: a configurable system for assessing pathogenicity of genetic variants

UNC Libraries(2020)10.17615/0r6z-dk65

N/A

0DataRank · unranked

0 citations

Kevin Riehle, Heidi L. Rehm, Rajarshi Ghosh, Tristan H Nelson, Aaron B. Baker +16 more

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

UNC Libraries(2020)10.17615/x7nz-xc34

N/A

0DataRank · unranked

0 citations

Levi A. Garraway, Elizabeth T. DeChene, Heidi L. Rehm, Matthew C. Dulik, James P. Evans +12 more

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

UNC Libraries(2020)10.17615/pbds-w495

N/A

0DataRank · unranked

0 citations

David Craig, Liming Qu, Jonathan L. Haines, Taniesha Morgan, Mark A. Sager +95 more

A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis

Kidney International(2021)10.1016/j.kint.2021.05.037

N/A

0DataRank · unranked

24 citations

Ian B. Stanaway, Gail P. Jarvik, Mark Lambie, Johann Morelle, Jeffrey Perl +84 more

What improves the likelihood of people receiving genetic test results communicating to their families about genetic risk?

Patient Education and Counseling(2021)10.1016/j.pec.2021.01.001

N/A

0DataRank · unranked

15 citations

Sukh Makhnoon, Brian H. Shirts, Stephanie M. Fullerton, Eric B. Larson, James D. Ralston +5 more

The genetic architecture of plasma kynurenine includes cardiometabolic disease mechanisms associated with the SH2B3 gene

Scientific Reports(2021)10.1038/s41598-021-95154-9

N/A

0DataRank · unranked

11 citations

Chuan Wang, Mingjian Shi, Ali Manouchehri, Katherine T. Murray, Matthew B. Murphy +12 more

Usefulness of mobile apps for communication of genetic test results to at-risk family members in a U.S. integrated health system: A qualitative approach from user-testing

Health Policy and Technology(2021)10.1016/j.hlpt.2021.100511

N/A

0DataRank · unranked

8 citations

Aaron Scrol, Chethan Jujjavarapu, Gail P. Jarvik, Nora B. Henrikson, Cameron B. Haas

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w

N/A

0DataRank · unranked

8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 more

ShareDNA: a smartphone app to facilitate family communication of genetic results

BMC Medical Genomics(2021)10.1186/s12920-020-00864-0

N/A

0DataRank · unranked

8 citations

Jeevan Anandasakaran, Laura M. Amendola, Cameron B. Haas, Elizabeth Zampino, Nora B. Henrikson +3 more

Gail P. Jarvik

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