Albert V. Smith

ORCID: 0000-0003-1942-5845

Also affiliated with Stanford University

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

10.9Author DataRank

Indexed papers

8in 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 8 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.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Papers

Driven by 102 papers — median percentile 72. Top paper: “Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals”.

Polygenic prediction of educational attainment within and between families from genome-wide association analyses in 3 million individuals

Nature Genetics(2022)10.1038/s41588-022-01016-z

N/A

8.1DataRank · unranked

699 citations

Yeda Wu, Nancy Wang, Hariharan Jayashankar, Michael Bennett, Seyed Moeen Nehzati +94 more

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Cerebral small vessel disease genomics and its implications across the lifespan

Nature Communications(2020)10.1038/s41467-020-19111-2

N/A

4.3DataRank · unranked

209 citations

Hideaki Suzuki, Xueqiu Jian, Chloé Sarnowski, Tavia E. Evans, Joshua C. Bis +94 more

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00935-7

N/A

4.0DataRank · unranked

191 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 more

Genome-wide association meta-analysis identifies 17 loci associated with nonalcoholic fatty liver disease

Nature Genetics(2023)10.1038/s41588-023-01497-6

N/A

3.8DataRank · unranked

208 citations

Xiaomeng Du, Annapurna Kuppa, Mary F. Feitosa, Lawrence F. Bielak, Jeffrey R. O’Connell +32 more

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Nature Genetics(2020)10.1038/s41588-020-00713-x

N/A

3.7DataRank · unranked

242 citations

Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook +94 more

Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

Cell Genomics(2022)10.1016/j.xgen.2021.100084

Top 10%

2.1DataRank

Top 10%82 citations

Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek +95 more

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Nature Communications(2020)10.1038/s41467-020-20086-3

N/A

1.6DataRank · unranked

91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +95 more

Allele-specific variation atAPOEincreases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer’s disease and myocardial infarction

Human Molecular Genetics(2021)10.1093/hmg/ddab096

N/A

1.2DataRank · unranked

41 citations

Bratati Kahali, Annapurna Kuppa, Yanhua Chen, Xiaomeng Du, Mary F. Feitosa +31 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

Gene-educational attainment interactions in a multi-ancestry genome-wide meta-analysis identify novel blood pressure loci

Molecular Psychiatry(2020)10.1038/s41380-020-0719-3

N/A

0.810DataRank · unranked

25 citations

Yun Ju Sung, Raymond Noordam, Thomas W. Winkler, Mary F. Feitosa, Karen Schwander +95 more

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

Nature Genetics(2023)10.1038/s41588-023-01314-0

N/A

0.794DataRank · unranked

198 citations

Abril G. Izquierdo, Jing Chen, Richard Packer, Robert J. Hall, Anna L. Guyatt +95 more

Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability

Nature Communications(2021)10.1038/s41467-020-19366-9

N/A

0.771DataRank · unranked

170 citations

Reedik Mägi, Jouke‐Jan Hottenga, Harald Grallert, John R. B. Perry, Nabila Bouatia‐Naji +95 more

Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

Nature Genetics(2023)10.1038/s41588-023-01518-4

N/A

0.753DataRank · unranked

150 citations

Maxime M. Bos, Hanna J. Barnes, Christian L. Lino Cardenas, Doris Wong, Haojie Lu +84 more

rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis

Journal of Hepatology(2020)10.1016/j.jhep.2020.08.027

N/A

0.744DataRank · unranked

142 citations

Kushala Abeysekera, Leon A. Adams, Elmar Aigner, Quentin M. Anstee, Jesús M. Bañales +93 more

Structural variation across 138,134 samples in the TOPMed consortium

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.25.525428

Top 27%

0.737DataRank

Top 27%18 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

Human Molecular Genetics(2021)10.1093/hmg/ddab252

Top 28%

0.724DataRank

Top 28%20 citations

Yao Hu, Quan Sun, Deepti Jain, Jai Broome, Ming‐Huei Chen +62 more

TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.006

N/A

0.701DataRank · unranked

106 citations

Jonathan D. Rosen, Quan Sun, Jiawen Chen, Marsha M. Wheeler, Ying Zhou +20 more

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.014

N/A

0.605DataRank · unranked

14 citations

Xiaolong Ma, Adrienne M. Stilp, Fulong Yu, Jason Bacon, Justin Wong +64 more

Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

PLoS ONE(2020)10.1371/journal.pone.0230815

N/A

0.574DataRank · unranked

45 citations

Denis Rybin, Lawrence F. Bielak, Mary F. Feitosa, Nora Franceschini, Yize Li +53 more

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Communications Biology(2022)10.1038/s42003-022-03448-z

N/A

0.553DataRank · unranked

39 citations

Humaira Rasheed, Alexander Teumer, Mathias Gorski, Bryce Rowan, Kira J. Stanzick +94 more

A genome-wide association study identifies genetic loci associated with specific lobar brain volumes

Communications Biology(2019)10.1038/s42003-019-0537-9

N/A

0.546DataRank · unranked

37 citations

Maria J. Knol, Ganesh Chauhan, Claudia L. Satizábal, Albert V. Smith, Edith Hofer +57 more

Association of Genetic Variants with Postsurgical Pain: A Systematic Review and Meta-analyses

Anesthesiology(2023)10.1097/aln.0000000000004677

N/A

0.538DataRank · unranked

35 citations

Mark MacEachern, Adam Akbar, Christian Bolton, Victor Lin, Albert V. Smith +3 more

Rare genetic variants explain missing heritability in smoking

Nature Human Behaviour(2022)10.1038/s41562-022-01408-5

N/A

0.520DataRank · unranked

31 citations

Luke M. Evans, Allison Fialkowski, Donna K. Arnett, Allison E. Ashley‐Koch, Kathleen C. Barnes +85 more

Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

PLoS ONE(2020)10.1371/journal.pone.0230035

N/A

0.513DataRank · unranked

8 citations

Yi-Ping Fu, Michael R. Brown, Joshua C. Bis, Paul S. de Vries, Mary F. Feitosa +40 more

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

EBioMedicine(2021)10.1016/j.ebiom.2020.103157

N/A

0.505DataRank · unranked

28 citations

Kelsey Grinde, Jennifer A. Brody, Charles E. Breeze, Laura M. Raffield, Josyf C. Mychaleckyj +68 more

FixItFelix: improving genomic analysis by fixing reference errors

Genome biology(2023)10.1186/s13059-023-02863-7

N/A

0.500DataRank · unranked

27 citations

Jonathon LeFaive, Peter Orchard, Medhat Mahmoud, Luis F. Paulin, Jesse Farek +7 more

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.007

N/A

0.494DataRank · unranked

26 citations

Caitlin McHugh, Linda M. Polfus, Laura M. Raffield, Meher Preethi Boorgula, Thomas W. Blackwell +88 more

Robust, flexible, and scalable tests for Hardy–Weinberg equilibrium across diverse ancestries

Genetics(2021)10.1093/genetics/iyab044

N/A

0.489DataRank · unranked

25 citations

Thomas W. Blackwell, Jonathon LeFaive, Mariza de Andrade, John Barnard, Kathleen C. Barnes +42 more

Genome-Wide Association Studies Identify CHRNA5/3 and HTR4 in the Development of Airflow Obstruction

UNC Libraries(2020)10.17615/n8t6-g528

N/A

0.457DataRank · unranked

20 citations

Amy R. Bentley, Lorna M. Lopez, Amund Gulsvik, Ivan Curjuric, Tamara B. Harris +27 more

A Noncoding Variant Near PPP1R3B Promotes Liver Glycogen Storage and MetS, but Protects Against Myocardial Infarction

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa855

N/A

0.449DataRank · unranked

19 citations

Yue Chen, Mary F. Feitosa, Lawrence F. Bielak, Jeffrey R. O’Connell, Solomon K. Musani +41 more

Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research

Journal of the American Medical Informatics Association(2023)10.1093/jamia/ocad048

N/A

0.442DataRank · unranked

18 citations

Paul Avillach, Rebecca Boyles, Kira Bradford, Steven J. Cox, Brandi N. Davis‐Dusenbery +53 more

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Nature Communications(2022)10.1038/s41467-022-35354-7

N/A

0.442DataRank · unranked

18 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more

Investigating Gene–Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits

Diabetes(2023)10.2337/db22-0851

N/A

0.425DataRank · unranked

16 citations

Maura E. Walker, Sheila M. Gaynor, Jennifer Wessel, Daniel DiCorpo, Jiantao Ma +66 more

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.003

N/A

0.416DataRank · unranked

15 citations

Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A. Holdcraft, Donna K. Arnett +69 more

Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

Nature Aging(2024)10.1038/s43587-024-00647-7

N/A

0.406DataRank · unranked

14 citations

Michael A. Raddatz, Yash Pershad, Daniel Nachun, Kent D. Taylor, Xiuqing Guo +40 more

Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100013

N/A

0.406DataRank · unranked

14 citations

Melissa A. Richard, Solomon K. Musani, Yun Ju Sung, Thomas W. Winkler, Karen Schwander +95 more

Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy

American Journal of Ophthalmology(2021)10.1016/j.ajo.2021.06.014

N/A

0.406DataRank · unranked

14 citations

Gayatri Susarla, Lynn K. Stanwyck, John M. Rouhana, Ashley Li, Samuela Pollack +25 more

The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

Science Advances(2023)10.1126/sciadv.abm4945

N/A

0.396DataRank · unranked

13 citations

Cecelia Laurie, Jai Broome, Kent D. Taylor, Xiuqing Guo, Alan R. Shuldiner +82 more

Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

medRxiv(2020)10.1101/2020.12.09.20246736

N/A

0.360DataRank · unranked

10 citations

Adrienne M. Stilp, Caitlin McHugh, Shuquan Rao, Deepti Jain, Xiuwen Zheng +74 more

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100163

N/A

0.360DataRank · unranked

10 citations

Virginia Fisher, Xuan Deng, Jennifer A. Brody, Misa Graff, Elise Lim +57 more

Clonal hematopoiesis is driven by aberrant activation of TCL1A

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.10.471810

N/A

0.360DataRank · unranked

10 citations

Jayakrishnan Gopakumar, Bala Bharathi Burugula, Md Mesbah Uddin, Nikolaus Jahn, Julia A. Belk +95 more

Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.120.003258

N/A

0.360DataRank · unranked

10 citations

Latchezar Dimitrov, Shyh‐Huei Chen, Lawrence F. Bielak, Joshua C. Bis, Mary F. Feitosa +37 more

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization

Wellcome Open Research(2023)10.12688/wellcomeopenres.18754.1

N/A

0.357DataRank · unranked

7 citations

Natasha Hui Jin Ng, Juan Fernandez, Rebecca S. Fine, Eleanor Wheeler, Jennifer Wessel +95 more

Structural variation across 138,134 samples in the TOPMed consortium

Research Square(2023)10.21203/rs.3.rs-2515453/v1

N/A

0.345DataRank · unranked

9 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Rare and low-frequency exonic variants and gene-by-smoking interactions in pulmonary function

Scientific Reports(2021)10.1038/s41598-021-98120-7

N/A

0.331DataRank · unranked

5 citations

Victoria E. Jackson, Albert V. Smith, Han Chen, Traci M. Bartz, Colleen M. Sitlani +42 more

Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program

PLoS ONE(2021)10.1371/journal.pone.0253611

N/A

0.330DataRank · unranked

8 citations

Han Chen, Mary L. Biggs, Sylvia Wassertheil‐Smoller, Jan Bressler, Marguerite R. Irvin +24 more

Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential

Cancer Epidemiology Biomarkers & Prevention(2023)10.1158/1055-9965.epi-23-0305

N/A

0.330DataRank · unranked

8 citations

Eric A. Whitsel, Alex P. Reiner, Stephen S. Rich, Jerome I. Rotter, Kent D. Taylor +9 more

Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

Nature Communications(2024)10.1038/s41467-024-48394-y

N/A

0.330DataRank · unranked

8 citations

Surya B. Chhetri, Carla J. Connelly, Margaret A. Taub, Matthew P. Conomos, Joshua S. Weinstock +95 more

Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program

medRxiv(2021)10.1101/2021.12.16.21267871

N/A

0.292DataRank · unranked

6 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more

GAWMerge expands GWAS sample size and diversity by combining array-based genotyping and whole-genome sequencing

Communications Biology(2022)10.1038/s42003-022-03738-6

N/A

0.269DataRank · unranked

3 citations

Fang Fang, Nathan Gaddis, Dana B. Hancock, Michael H. Cho, John E. Hokanson +8 more

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

Digital Commons@Becker (Washington University School of Medicine)(2020)10.17615/5y99-4w88

N/A

0.269DataRank · unranked

5 citations

Terho Lehtimäki, P. Eline Slagboom, Albert V. Smith, Dennis O. Mook‐Kanamori, Paul Elliott +93 more

Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.23.167759

N/A

0.269DataRank · unranked

5 citations

Thomas W. Blackwell, Jonathon LeFaive, Mariza de Andrade, John Barnard, Kathleen C. Barnes +42 more

Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00979-9

N/A

0.246DataRank · unranked

4 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 more

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

medRxiv(2024)10.1101/2024.04.16.24305851

N/A

0.241DataRank · unranked

4 citations

Xiaolong Ma, Adrienne M. Stilp, Fulong Yu, Jason Bacon, Justin Wong +61 more

Genetic architecture and analysis practices of circulating metabolites in the NHLBI Trans-Omics for Precision Medicine Program

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.022

N/A

0.217DataRank · unranked

3 citations

Franklin P Ockerman, Laura Y. Zhou, Megan L. Grove, Taryn Alkis, J. A. Barnard +31 more

Fixing reference errors efficiently improves sequencing results

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.07.18.500506

Top 65%

0.208DataRank

Top 65%3 citations

Jonathon LeFaive, Peter Orchard, Medhat Mahmoud, Luis F. Paulin, Jesse Farek +7 more

Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function

UNC Libraries(2020)10.17615/6mem-qn63

N/A

0.208DataRank · unranked

3 citations

Matthew Kowgier, Tamara B. Harris, Wei Gao, Xiangjun Gu, Rasika A. Mathias +27 more

Genetic Associations of Persistent Opioid Use After Surgery Point to OPRM1 but Not Other Opioid‐Related Loci as the Main Driver of Opioid Use Disorder

Genetic Epidemiology(2024)10.1002/gepi.22588

N/A

0.184DataRank · unranked

2 citations

Vidhya Gunaseelan, Albert V. Smith, Gonçalo R. Abecasis, Daniel B. Larach, Matthew Zawistowski +3 more

Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits

medRxiv(2022)10.1101/2022.07.26.22278077

N/A

0.182DataRank · unranked

1 citations

Maura E. Walker, Sheila M. Gaynor, Jennifer Wessel, Daniel DiCorpo, Jiantao Ma +66 more

Association of low-frequency and rare coding variants with information processing speed

Translational Psychiatry(2021)10.1038/s41398-021-01736-6

N/A

0.165DataRank · unranked

2 citations

Gail Davies, Albert V. Smith, Yasaman Saba, Joshua C. Bis, Xueqiu Jian +50 more

Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations

Nature Communications(2025)10.1038/s41467-025-64236-x

N/A

0.165DataRank · unranked

2 citations

Sharjeel A. Chaudhry, Μαρία Ιωάννου, Maria Viskadourou, Paula Reventún, Yasminka A. Jakubek +49 more

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study

medRxiv(2023)10.1101/2023.06.28.23291966

N/A

0.146DataRank · unranked

1 citations

Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A. Holdcraft, Donna K. Arnett +69 more

Genome-Wide Association Studies of MRI-Defined Brain Infarcts: Meta-Analysis From the CHARGE Consortium * Supplemental Appendix

UNC Libraries(2020)10.17615/1epm-k923

Top 73%

0.105DataRank

Top 73%1 citations

A. Beiser, J. I. Rotter, G. Eiriksdottir, M. FORNAGE, C. Enzinger +27 more

General Kernel Machine Methods for Multi‐Omics Integration and Genome‐Wide Association Testing With Related Individuals

Genetic Epidemiology(2025)10.1002/gepi.22610

N/A

0.104DataRank · unranked

1 citations

Ni Zhao, Anna V. Mikhaylova, Angela Zhang, Wodan Ling, Florian Thibord +25 more

Validation of human telomere length trans-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as novel human telomere length regulation genes

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.12.548702

N/A

0.104DataRank · unranked

1 citations

Surya B. Chhetri, Carla J. Connelly, Margaret A. Taub, Matthew P. Conomos, Joshua S. Weinstock +93 more

Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

UNC Libraries(2020)10.17615/aapr-pr41

N/A

0.104DataRank · unranked

1 citations

Niels Grarup, Albert Hofman, Lenore J. Launer, David C. Liewald, Albert V. Smith +76 more

Genome-wide gene by sleepiness interaction analysis for sleep apnea

SLEEP(2025)10.1093/sleep/zsaf212

N/A

0.104DataRank · unranked

1 citations

Nuzulul Kurniansyah, Jiwon Lee, Sina A. Gharib, Yushan Xu, Yiyan Zhang +80 more

Multi-Ethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI

MURAL - Maynooth University Research Archive Library (National University of Ireland, Maynooth)(2020)10.17615/8trn-p892

N/A

0DataRank · unranked

0 citations

W. T. Longstreth, Reinhold Schmidt, Paul Freudenberger, Pamela J. Schreiner, Stella Trompet +95 more

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

UNC Libraries(2020)10.17615/m864-xv86

N/A

0DataRank · unranked

0 citations

Lisa R. Yanek, Kjell Nikus, Salman M. Tajuddin, Jussi Hernesniemi, Dawn Waterworth +95 more

A Meta-analysis of Four Genome-Wide Association Studies of Survival to Age 90 Years or Older: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

Data Archiving and Networked Services (DANS)(2020)10.17615/rjmx-zn51

N/A

0DataRank · unranked

0 citations

Albert Hofman, Yurii S. Aulchenko, Lene Christiansen, Anne B. Newman, Robert M. Kaplan +27 more

Genome-Wide Joint Meta-Analysis of SNP and SNP-by-Smoking Interaction Identifies Novel Loci for Pulmonary Function

UNC Libraries(2020)10.17615/2z2d-ex03

N/A

0DataRank · unranked

0 citations

Jason Z. Liu, Joanna Smolonska, Kristin M. Burkart, Paul Elliott, Alisa K. Manning +27 more

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

UNC Libraries(2020)10.17615/a384-d483

N/A

0DataRank · unranked

0 citations

Jerome I. Rotter, Alex P. Reiner, André G. Uitterlinden, Gonçalo R. Abecasis, Digna R. Velez Edwards +95 more

Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants

Genetics(2023)10.1093/genetics/iyad115

N/A

0DataRank · unranked

10 citations

Dafni A. Glinos, Eric Boerwinkle, Peter J. Castaldi, Dawood Darbar, Mariza de Andrade +28 more

Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

UNC Libraries(2020)10.17615/xs3t-3334

N/A

0DataRank · unranked

0 citations

Annette L. Fitzpatrick, Luigi Ferrucci, Paul M. Ridker, Bertram Müller-Myhsok, Arezoo Assareh +95 more

Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.21.959312

N/A

0DataRank · unranked

0 citations

Yi‐Ping Fu, Michael R. Brown, Joshua C. Bis, Paul S. de Vries, Mary F. Feitosa +40 more

FTO genotype is associated with phenotypic variability of body mass index

UNC Libraries(2020)10.17615/yvv7-bx40

N/A

0DataRank · unranked

0 citations

Ayşe Demirkan, David Hadley, Cameron D. Palmer, Sarah E. Medland, Ruth J. F. Loos +27 more

Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

UNC Libraries(2024)10.17615/zpcz-6n16

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0 citations

Mary F. Feitosa, D.W. Bowden, N. Franceschini, L.M. Raffield, Daniël Bos +37 more

Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose

UNC Libraries(2024)10.17615/sj56-cj53

N/A

0DataRank · unranked

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Salman M. Tajuddin, Linda Kao, B.H. Smith, A. Correa, Sheelakumari Raghavan +52 more

Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

UNC Libraries(2024)10.17615/vs68-ca81

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Ryan L. Minster, Fernando D. Martínez, Dawood Darbar, Juan M. Peralta, Barbara A. Konkle +93 more

Gene-Excessive Sleepiness Interactions Suggest Treatment Targets for Obstructive Sleep Apnea Subtype

medRxiv(2024)10.1101/2024.10.25.24316158

N/A

0DataRank · unranked

0 citations

Nuzulul Kurniansyah, Jiwon Lee, Sina A. Gharib, Yushan Xu, Yiyan Zhang +31 more

Multi-ancestry genome-wide association analyses incorporating SNP-by-psychosocial interactions identify novel loci for serum lipids

Translational Psychiatry(2025)10.1038/s41398-025-03418-z

N/A

0DataRank · unranked

0 citations

Michael R. Brown, Solomon K. Musani, Karen Schwander, Thomas W. Winkler, Mario Sims +93 more

Associations between Ambient Air Pollutants and Clonal Hematopoiesis of Indeterminate Potential.

UNC Libraries(2025)10.17615/fdg0-0818

N/A

0DataRank · unranked

0 citations

Alexander G. Bick, JOANN E. MANSON, Jerome I. Rotter, Claire L. Leiser, Albert V. Smith +9 more

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

UNC Libraries(2025)10.17615/cdn0-cm52

N/A

0DataRank · unranked

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Russell P. Tracy, Jill M. Johnsen, Hind Bouzid, Nicholas L. Smith, Katherine P. Prothro +95 more

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

UNC Libraries(2025)10.17615/5tss-f273

N/A

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0 citations

Eric Boerwinkle, Yash Pershad, K.E. North, Fulong Yu, Center, Regeneron Genetics +66 more

Serum microRNA expression quantitative trait loci in children with asthma colocalize with asthma-related GWAS results

npj Genomic Medicine(2025)10.1038/s41525-025-00510-7

N/A

0DataRank · unranked

1 citations

Anshul Tiwari, Rinku Sharma, Kevin Mendez, Jiang Li, Sofina Begum +9 more

Sparse allele vectors and the savvy software suite

Bioinformatics(2021)10.1093/bioinformatics/btab378

N/A

0DataRank · unranked

15 citations

Albert V. Smith, Hyun Min Kang, Gonçalo R. Abecasis, Jonathon LeFaive

Ehret GB, Munroe PB, Rice KM, Bochud M, Johnson AD, Chasman DI et al. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature 2011; 478: 103-109

WOS(2020)10.17615/brds-5n12

N/A

0DataRank · unranked

0 citations

Simon Heath, Abbas Dehghan, Feng Zhang, Jing Zhao, Jian’an Luan +27 more

Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

UNC Libraries(2020)10.17615/frhz-yk87

N/A

0DataRank · unranked

0 citations

Juan M. Peralta, Olivia Weeks, Gudnason, Vilmunder, Kurt Lohman, Andrew D. Johnson +63 more

Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium

UNC Libraries(2020)10.17615/xrs5-6v14

N/A

0DataRank · unranked

0 citations

James Wilson, Bouwe P. Krijthe, Nicholas L. Smith, Susan R. Heckbert, Kerri L. Wiggins +27 more

NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium

UNC Libraries(2020)10.17615/svd7-zw53

N/A

0DataRank · unranked

0 citations

Lenore J. Launer, Barbara McKnight, Alan R. Shuldiner, Tamara B. Harris, Ulf Gyllensten +27 more

Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins

Data Archiving and Networked Services (DANS)(2020)10.17615/b2qf-7d72

N/A

0DataRank · unranked

0 citations

Daniel I. Chasman, Neil R. Poulter, Iris Postmus, Catherine E. de Keyser, David J. Stott +27 more

Molecular mechanisms underlying variations in lung function: a systems genetics analysis

UNC Libraries(2020)10.17615/nsqr-r935

N/A

0DataRank · unranked

0 citations

Yunlong Nie, Ma’en Obeidat, H. Schulz, Andrew J. Sandford, Albert V. Smith +27 more

Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function

UNC Libraries(2020)10.17615/d3kg-q519

N/A

0DataRank · unranked

0 citations

Patricia A. Cassano, Jing Zhao, Guðný Eiríksdóttir, Gauti Kjartan Gíslason, Jennifer E. Huffman +27 more

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

UNC Libraries(2020)10.17615/s8sd-h432

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Todd L. Edwards, Jin Li, John M. Starr, Eric Boerwinkle, Yingchang Lu +92 more

Accounting for population structure in genetic studies of cystic fibrosis

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100117

N/A

0DataRank · unranked

6 citations

Adrienne M. Stilp, William W. Gordon, Jai Broome, Stephanie M. Gogarten, Hua Ling +20 more

Multiple Loci Are Associated with White Blood Cell Phenotypes

UNC Libraries(2020)10.17615/52kr-j158

N/A

0DataRank · unranked

0 citations

Vasiliki Lagou, Kent D. Taylor, Daniela Toniolo, Uwe Völker, James Wilson +27 more

Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

UNC Libraries(2020)10.17615/y892-y714

N/A

0DataRank · unranked

0 citations

Wen‐Chi Hsueh, Eric Orwoll, Serkalem Demissie, Liisa Byberg, Arjun Verma +95 more

Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways

UNC Libraries(2020)10.17615/qy4d-rv77

N/A

0DataRank · unranked

0 citations

Albert V. Smith, Stefan Gustafsson, Laura J. Rasmussen‐Torvik, J. Wouter Jukema, P. Johnson +27 more

Genetic diversity is a predictor of mortality in humans

UNC Libraries(2020)10.17615/kwh0-eh07

N/A

0DataRank · unranked

0 citations

John M. Starr, David A. Bennett, Kathryn L. Lunetta, Hans J. Grabe, Lei Yu +47 more

Tutorial: a statistical genetics guide to identifying HLA alleles driving complex disease

Nature Protocols(2023)10.1038/s41596-023-00853-4

N/A

0DataRank · unranked

44 citations

Saisriram Gurajala, Michelle Curtis, Yang Luo, Wanson Choi, Kazuyoshi Ishigaki +14 more

Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks

UNC Libraries(2020)10.17615/sbz9-wg52

N/A

0DataRank · unranked

0 citations

Rebecca D. Jackson, Valeska Redon, Gina M. Peloso, Joshua C. Bis, Arend Voorman +27 more

Albert V. Smith

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