Joshua C. Bis

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

10in 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 10 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.

Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

Nature Communications(2021)10.1038/s41467-021-22491-8

Top 6%

3.9DataRank

Top 6%339 citations

Sonia Moreno–Grau, Niccoló Tesi, Benjamin Grenier‐Boley, Víctor Andrade, Iris E. Jansen +95 more

Papers

Driven by 142 papers — median percentile 73. Top paper: “Inherited causes of clonal haematopoiesis in 97,691 whole genomes”.

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Nature(2020)10.1038/s41586-020-2819-2

N/A

11.6DataRank · unranked

748 citations

Joshua S. Weinstock, Satish K. Nandakumar, Charles P. Fulco, Erik L. Bao, Seyedeh M. Zekavat +95 more

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Nature Genetics(2022)10.1038/s41588-021-00997-7

N/A

7.2DataRank · unranked

363 citations

Deepti Jain, Zhili Zheng, TOPMed Anthropometry Working Group, Stella Aslibekyan, Diane M. Becker +95 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

Genetic diversity fuels gene discovery for tobacco and alcohol use

Nature(2022)10.1038/s41586-022-05477-4

N/A

5.9DataRank · unranked

513 citations

Xingyan Wang, Fang Chen, Seon-Kyeong Jang, Mengzhen Liu, Chen Wang +95 more

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Nature Genetics(2020)10.1038/s41588-020-0676-4

N/A

5.3DataRank · unranked

295 citations

Zilin Li, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen +88 more

Clonal haematopoiesis and risk of chronic liver disease

Nature(2023)10.1038/s41586-023-05857-4

N/A

4.5DataRank · unranked

204 citations

Connor A. Emdin, Alexander G. Bick, Seyedeh M. Zekavat, Abhishek Niroula, James P. Pirruccello +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

Cholesteryl ester transfer protein (CETP) as a drug target for cardiovascular disease

Nature Communications(2021)10.1038/s41467-021-25703-3

N/A

4.0DataRank · unranked

143 citations

Nicholas B. Hunt, María Gordillo‐Marañón, Pimphen Charoen, Fotios Drenos, Mika Kivimäki +18 more

Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

Nature Communications(2021)10.1038/s41467-021-22491-8

Top 6%

3.9DataRank

Top 6%339 citations

Sonia Moreno–Grau, Niccoló Tesi, Benjamin Grenier‐Boley, Víctor Andrade, Iris E. Jansen +95 more

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 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

52 Genetic Loci Influencing Myocardial Mass

Journal of the American College of Cardiology(2016)10.1016/j.jacc.2016.07.729

N/A

2.4DataRank · unranked

135 citations

Jessica van Setten, Niek Verweij, Georg Vogler, Matthew T. Maurano, Xinchen Wang +172 more

A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

Nature Communications(2022)10.1038/s41467-022-31080-2

N/A

2.1DataRank · unranked

80 citations

Matthew Goodman, Tanika N. Kelly, Tali Elfassy, Kerri L. Wiggins, Joshua C. Bis +32 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

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

Nature(2023)10.1038/s41586-023-05806-1

N/A

2.1DataRank · unranked

107 citations

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

Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults

Nature Communications(2020)10.1038/s41467-020-18367-y

Top 12%

1.8DataRank

Top 12%109 citations

Gennady V. Roshchupkin, Hieab H.H. Adams, Maria J. Knol, Honghuang Lin, Shuo Li +87 more

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

Nature Communications(2022)10.1038/s41467-022-33510-7

N/A

1.6DataRank · unranked

75 citations

Xihao Li, Zilin Li, Akhil Pampana, David Zhang, Joseph Park +95 more

Genome sequencing unveils a regulatory landscape of platelet reactivity

Nature Communications(2021)10.1038/s41467-021-23470-9

N/A

1.5DataRank · unranked

54 citations

Ming‐Huei Chen, Benjamin A.T. Rodriguez, Lisa R. Yanek, Arunoday Bhan, Brady Gaynor +94 more

Association of mitochondrial DNA copy number with cardiometabolic diseases

Cell Genomics(2021)10.1016/j.xgen.2021.100006

N/A

1.4DataRank · unranked

62 citations

Ryan J. Longchamps, Kerri L. Wiggins, Laura M. Raffield, Lawrence F. Bielak, Wei Zhao +33 more

Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

Stroke(2021)10.1161/strokeaha.120.031792

Top 16%

1.3DataRank

Top 16%38 citations

Jeffrey W. Haessler, Regina Manansala, Kerri L. Wiggins, Arden Moscati, Alexa Beiser +34 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

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Nature Genetics(2022)10.1038/s41588-022-01225-6

N/A

1.2DataRank · unranked

63 citations

Corbin Quick, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen +95 more

Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

Nature Communications(2022)10.1038/s41467-022-32275-3

N/A

1.1DataRank · unranked

63 citations

Daniel H. Katz, Julián Ávila-Pacheco, Alexander G. Bick, Akhil Pampana, Jeremy Robbins +95 more

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

Nature Genetics(2014)10.1038/ng.3043

N/A

1.1DataRank · unranked

1956 citations

NeuroGenetics Research Consortium (NGRC), The Ashkenazi Jewish Dataset Investigator, Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE), Alzheimer Genetic Analysis Group, Nathan Pankratz +49 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

Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

Journal of the American Heart Association(2023)10.1161/jaha.122.029090

N/A

0.920DataRank · unranked

30 citations

Xianbang Sun, Yuankai Zhang, Wenqing Jiang, M M Lai, Kerri L. Wiggins +40 more

Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry: A Prospective Meta-Analysis From the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

UNC Libraries(2020)10.17615/egzf-8a86

N/A

0.862DataRank · unranked

12 citations

Nicholas L. Smith, Joanne M. Murabito, Christopher J. O’Donnell, Ervin R. Fox, Alanna C. Morrison +33 more

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

Nature Communications(2021)10.1038/s41467-021-23655-2

N/A

0.840DataRank · unranked

21 citations

Xiuwen Zheng, Cecelia Laurie, Stephanie M. Gogarten, Jennifer A. Brody, Matthew P. Conomos +91 more

Clonal Hematopoiesis Is Associated With Higher Risk of Stroke

Stroke(2021)10.1161/strokeaha.121.037388

N/A

0.801DataRank · unranked

208 citations

Seyedeh M. Zekavat, Jeffrey Haessler, Myriam Fornage, Laura M. Raffield, Md Mesbah Uddin +28 more

Clonal hematopoiesis is associated with protection from Alzheimer’s disease

Nature Medicine(2023)10.1038/s41591-023-02397-2

N/A

0.755DataRank · unranked

152 citations

Julia A. Belk, Max Jan, Yanyan Qi, Chloé Sarnowski, Sara A. Wirth +23 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

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

Identification of circulating proteins associated with general cognitive function among middle-aged and older adults

Communications Biology(2023)10.1038/s42003-023-05454-1

N/A

0.689DataRank · unranked

22 citations

Alison E. Fohner, Qiong Yang, Jennifer A. Brody, Gail Davies, Jie Yao +52 more

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

Nature Genetics(2023)10.1038/s41588-023-01553-1

N/A

0.681DataRank · unranked

31 citations

Ying Zhou, Adrienne M. Stilp, Jason Bacon, Justin Wong, Zuhal Özcan +46 more

New insights on the genetic etiology of Alzheimer’s and related dementia

medRxiv(2020)10.1101/2020.10.01.20200659

N/A

0.677DataRank · unranked

90 citations

Fahri Küçükali, Iris E. Jansen, Víctor Andrade, Sonia Moreno–Grau, Najaf Amin +95 more

Polygenic prediction of body mass index and obesity through the life course and across ancestries

Nature Medicine(2025)10.1038/s41591-025-03827-z

N/A

0.665DataRank · unranked

34 citations

Kaitlin H Wade, Qin Hui, Joshua Arias, Xianyong Yin, Malene R. Christiansen +95 more

The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations

Frontiers in Endocrinology(2022)10.3389/fendo.2022.863893

N/A

0.642DataRank · unranked

21 citations

Shing Wan Choi, Nathalie Chami, Eric Boerwinkle, Myriam Fornage, Susan Redline +36 more

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

Stroke(2020)10.1161/strokeaha.120.029123

N/A

0.637DataRank · unranked

69 citations

Hyacinth I. Hyacinth, Joshua C. Bis, Steven J. Kittner, Braxton D. Mitchell, Yu-Ching Cheng +43 more

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0.628DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 more

Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

Nature Genetics(2023)10.1038/s41588-022-01282-x

N/A

0.606DataRank · unranked

56 citations

Xingyan Wang, Seon-Kyeong Jang, Bryan C. Quach, J. Dylan Weissenkampen, Chachrit Khunsriraksakul +85 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

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Nature Communications(2022)10.1038/s41467-022-32821-z

N/A

0.596DataRank · unranked

52 citations

Najim Lahrouchi, Aaron Isaacs, ThuyVy Duong, Luisa Foco, Farah Ahmed +95 more

Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups

Nature Communications(2023)10.1038/s41467-023-38990-9

N/A

0.578DataRank · unranked

46 citations

Matthew Goodman, Alyna Khan, Jiongming Wang, Elena V. Feofanova, Joshua C. Bis +38 more

Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia

JAMA Network Open(2024)10.1001/jamanetworkopen.2024.12824

N/A

0.571DataRank · unranked

19 citations

Aïcha Soumaré, Joshua C. Bis, Ida Surakka, Tuuli Jürgenson, Pierre Joly +29 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

Genomic and phenomic landscape of clonal hematopoiesis in over a million ancestrally diverse participants

medRxiv(2022)10.1101/2022.07.29.22278015

Top 37%

0.528DataRank

Top 37%13 citations

Zhi Yu, Joshua S. Weinstock, Abhishek Niroula, Satoshi Koyama, Tetsushi Nakao +83 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

Rare variant contribution to the heritability of coronary artery disease

Nature Communications(2024)10.1038/s41467-024-52939-6

N/A

0.513DataRank · unranked

16 citations

Shoa L. Clarke, Gaëlle Auguste, Natalie R. Hasbani, Alanna C. Morrison, Adam S. Heath +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

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

Multiomics integrative analysis identifies APOE allele-specific blood biomarkers associated to Alzheimer’s disease etiopathogenesis

Aging(2021)10.18632/aging.202950

N/A

0.510DataRank · unranked

29 citations

Alzheimer’s Disease Neuroimaging Initiative (ADNI)*, Sonia Moreno–Grau, Shahzad Ahmad, Antonio González-Pérez, Itziar de Rojas +32 more

Proteomics and Population Biology in the Cardiovascular Health Study (CHS): design of a study with mentored access and active data sharing

European Journal of Epidemiology(2022)10.1007/s10654-022-00888-z

N/A

0.505DataRank · unranked

28 citations

Caitlin McHugh, Jennifer A. Brody, Joshua C. Bis, Colleen M. Sitlani, Traci M. Bartz +33 more

Association of Plasma YKL-40 With MRI, CSF, and Cognitive Markers of Brain Health and Dementia

Neurology(2024)10.1212/wnl.0000000000208075

N/A

0.505DataRank · unranked

28 citations

Jayandra J. Himali, Raquel Puerta, Alexa Beiser, Mitzi M. Gonzales, Claudia L. Satizábal +21 more

Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

Molecular Psychiatry(2021)10.1038/s41380-021-01087-0

N/A

0.483DataRank · unranked

24 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

Cystatin C and Cardiovascular Disease: A Mendelian Randomization Study

UNC Libraries(2020)10.17615/n5vd-xm37

N/A

0.477DataRank · unranked

23 citations

Björn O. Eriksen, Ivana Išgum, Annette Peters, Christopher D. O’Donnell, Christa Meisinger +67 more

Associations of Pulmonary Function with MRI Brain Volumes: A Coordinated Multi-Study Analysis

Journal of Alzheimer s Disease(2022)10.3233/jad-220667

N/A

0.477DataRank · unranked

23 citations

Joshua C. Bis, Elías F. Guðmundsson, Adrienne O’Donnell, Jeannette Simino, Amber Yaqub +35 more

Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries

Nature Genetics(2024)10.1038/s41588-024-01951-z

N/A

0.470DataRank · unranked

22 citations

Adrián I. Campos, Santiago Díaz‐Torres, Jill A. Rabinowitz, Zuriel Ceja, Brittany L. Mitchell +95 more

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

Nature Communications(2022)10.1038/s41467-022-28729-3

N/A

0.470DataRank · unranked

22 citations

Lingyan Chen, Paulina J. Stanczyk, Joanna M. M. Howson, Amy M. Mason, Stephen Burgess +91 more

Admixture mapping implicates 13q33.3 as ancestry-of-origin locus for Alzheimer disease in Hispanic and Latino populations

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100207

N/A

0.425DataRank · unranked

16 citations

Lisa A. Boyken, Elizabeth Blue, Kelsey Grinde, Rafael A. Nafikov, Harkirat Sohi +13 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

Genomic Studies Across the Lifespan Point to Early Mechanisms Determining Subcortical Volumes

Biological Psychiatry Cognitive Neuroscience and Neuroimaging(2021)10.1016/j.bpsc.2021.10.011

N/A

0.406DataRank · unranked

14 citations

Claudia L. Satizábal, Muralidharan Sargurupremraj, Aniket Mishra, Aïcha Soumaré, Alexandre Laurent +17 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

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

A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies

Nature Computational Science(2025)10.1038/s43588-024-00764-8

N/A

0.393DataRank · unranked

10 citations

Han Chen, Margaret Sunitha Selvaraj, Eric Van Buren, Hufeng Zhou, Yuxuan Wang +95 more

Genetic variants for head size share genes and pathways with cancer

Cell Reports Medicine(2024)10.1016/j.xcrm.2024.101529

N/A

0.380DataRank · unranked

10 citations

Raymond A. Poot, Tavia E. Evans, Claudia L. Satizábal, Aniket Mishra, Muralidharan Sargurupremraj +95 more

Selected social and lifestyle correlates of brain health markers: the Cross‐Cohort Collaboration Consortium

Alzheimer s & Dementia(2025)10.1002/alz.70148

Top 49%

0.363DataRank

Top 49%8 citations

Joshua C. Bis, Stefan Frenzel, Daniel Kojis, Jeannette Simino, Amber Yaqub +29 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

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

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

Determinants of mosaic chromosomal alteration fitness

Nature Communications(2024)10.1038/s41467-024-48190-8

N/A

0.345DataRank · unranked

9 citations

Taralynn Mack, Hannah Poisner, Yasminka A. Jakubek, Adrienne M. Stilp, Braxton D. Mitchell +39 more

Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel disease

Research Square(2024)10.21203/rs.3.rs-4535534/v1

N/A

0.331DataRank · unranked

5 citations

Ilana Caro, Daniel Western, Shinichi Namba, Na Sun, Shuji Kawaguchi +52 more

A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment

Journal of Thrombosis and Haemostasis(2023)10.1016/j.jtha.2023.11.027

N/A

0.330DataRank · unranked

8 citations

Gerard Temprano‐Sagrera, Jara Cárcel‐Márquez, Elena Muiño, Natàlia Cullell, Miquel Lledós +91 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

Epigenetic mechanisms underlying variation of IL-6, a well-established inflammation biomarker and risk factor for cardiovascular disease

Atherosclerosis(2025)10.1016/j.atherosclerosis.2025.120219

N/A

0.312DataRank · unranked

7 citations

Ulrike Peters, Yao Hu, Farah Ammous, Emelia J. Benjamin, Joshua C. Bis +31 more

Genome-wide association study meta-analysis of neurofilament light (NfL) levels in blood reveals novel loci related to neurodegeneration

Communications Biology(2024)10.1038/s42003-024-06804-3

N/A

0.312DataRank · unranked

7 citations

Mohammad Aslam Imtiaz, Aniket Mishra, Ruiqi Wang, Marisol Herrera-Rivero, Joshua C. Bis +29 more

Human plasma proteomic profile of clonal hematopoiesis

Nature Communications(2025)10.1038/s41467-025-66755-z

N/A

0.312DataRank · unranked

7 citations

Amélie Vromman, Ngoc Quynh Nguyen, Art Schuermans, Linke Li, Thiago Rentz +48 more

Genetic variants for head size share genes and pathways with cancer

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.15.191114

N/A

0.312DataRank · unranked

7 citations

Raymond A. Poot, Tavia E. Evans, Claudia L. Satizábal, Aniket Mishra, Sandra Van der Auwera +95 more

Single-Ancestry versus Multi-Ancestry Polygenic Risk Scores for CKD in Black American Populations

Journal of the American Society of Nephrology(2024)10.1681/asn.0000000000000437

N/A

0.292DataRank · unranked

6 citations

Amit Patki, Vinodh Srinivasasainagendra, Hemant K. Tiwari, Nicole D. Armstrong, Ninad S. Chaudhary +25 more

Frequency of Variants in Mendelian Alzheimer’s Disease Genes within the Alzheimer’s Disease Sequencing Project (ADSP)

medRxiv(2023)10.1101/2023.10.24.23297227

N/A

0.292DataRank · unranked

6 citations

Alexandra Scalici, Yanbing Wang, Honghuang Lin, Achilleas Pitsillides, Nancy L. Heard‐Costa +16 more

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Human Plasma Proteomic Profile of Clonal Hematopoiesis

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.25.550557

N/A

0.269DataRank · unranked

5 citations

Amélie Vromman, Ngoc Quynh Nguyen, Art Schuermans, Thiago Rentz, Shamsudheen Karuthedath Vellarikkal +44 more

A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.18.146423

N/A

0.269DataRank · unranked

5 citations

Leslie S. Emery, Jai Broome, Erin Buth, Alyna Khan, Cecelia Laurie +67 more

Association of Novel Genetic Loci With Circulating Fibrinogen Levels: A Genome-Wide Association Study in 6 Population-Based Cohorts

UNC Libraries(2020)10.17615/b6yn-gb03

N/A

0.269DataRank · unranked

5 citations

Susana Eyhermendy, Wendy L. McArdle, David P. Strachan, Melanie Kolz, Martin G. Larson +36 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

Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele

Nature Communications(2025)10.1038/s41467-025-58420-2

N/A

0.269DataRank · unranked

5 citations

Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu +93 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

Population Stratification at the Phenotypic Variance level and Implication for the Analysis of Whole Genome Sequencing Data from Multiple Studies

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.03.973420

N/A

0.241DataRank · unranked

4 citations

Xiuwen Zheng, Cecelia Laurie, Stephanie M. Gogarten, Jennifer A. Brody, Matthew P. Conomos +10 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

Genomic Variation Associated With Mortality Among Adults of European and African Ancestry With Heart Failure: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium

UNC Libraries(2020)10.17615/4tec-rx52

N/A

0.241DataRank · unranked

4 citations

Ying A. Wang, L. Adrienne Cupples, Patricia P. Chang, James T. Willerson, Eric Boerwinkle +29 more

Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance

Alzheimer s Research & Therapy(2024)10.1186/s13195-023-01376-6

N/A

0.208DataRank · unranked

3 citations

Jeannette Simino, Lianna Li, Fan Jiang, Joshua C. Bis, Gail Davies +62 more

Proteogenomics in cerebrospinal fluid and plasma reveals new biological fingerprint of cerebral small vessel disease

Nature Aging(2025)10.1038/s43587-025-01006-w

N/A

0.165DataRank · unranked

2 citations

Daniel Western, Shinichi Namba, Na Sun, Shuji Kawaguchi, Yunye He +56 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

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk

medRxiv(2023)10.1101/2023.08.14.23294063

N/A

0.165DataRank · unranked

2 citations

Rainer Malik, Omar El Bounkari, Natalie R. Hasbani, Jiang Li, Jennifer E. Huffman +60 more

WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE

medRxiv(2023)10.1101/2023.08.21.23293271

N/A

0.165DataRank · unranked

2 citations

Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu +95 more

Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals

Genome biology(2025)10.1186/s13059-025-03698-0

N/A

0.165DataRank · unranked

2 citations

Xihao Li, Zilin Li, Eric Van Buren, Sara Haidermota, Darina Postupaka +95 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

Methylome-wide association analyses of lipids and modifying effects of behavioral factors in diverse race and ethnicity participants

Clinical Epigenetics(2025)10.1186/s13148-025-01859-3

N/A

0.104DataRank · unranked

1 citations

Jeff Haessler, Jessica I. Lundin, Burcu F. Darst, Eric A. Whitsel, Megan L. Grove +32 more

The association between mitochondrial DNA copy number, low-density lipoprotein cholesterol, and cardiovascular disease risk

medRxiv(2022)10.1101/2022.10.23.22281418

N/A

0.104DataRank · unranked

1 citations

Xianbang Sun, Yuankai Zhang, Wenqing Jiang, Lai Meng, Kerri L. Wiggins +40 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

Determinants of mosaic chromosomal alteration fitness

medRxiv(2023)10.1101/2023.10.20.23297280

N/A

0.104DataRank · unranked

1 citations

Taralynn Mack, Hannah Poisner, Yasminka A. Jakubek, Adrienne M. Stilp, Braxton D. Mitchell +39 more

African ancestry genome-wide association study of blood pressure and hypertension identifies 25 novel loci through predicted gene expression

Research Square(2022)10.21203/rs.3.rs-1392991/v1

N/A

0.104DataRank · unranked

1 citations

Jingjing Liang, Ayush Giri, Jacob M. Keaton, Xiao Sun, Eric S. Torstenson +35 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

0DataRank · unranked

18 citations

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

A population‐based meta‐analysis of circulating GFAP for cognition and dementia risk

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51652

N/A

0DataRank · unranked

41 citations

Crystal Wiedner, Chen‐Pin Wang, Qianqian Liu, Joshua C. Bis, Chi Kong Li +27 more

A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

Nature Methods(2022)10.1038/s41592-022-01640-x

N/A

0DataRank · unranked

109 citations

Xihao Li, Hufeng Zhou, Sheila M. Gaynor, Margaret Sunitha Selvaraj, Theodore Arapoglou +95 more

Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease

Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring(2021)10.1002/dad2.12255

N/A

0DataRank · unranked

8 citations

William S. Bush, Alan E. Renton, Edoardo A. Marcora, Joshua C. Bis, Brian W. Kunkle +13 more

Adverse Cardiovascular Outcomes and Antihypertensive Treatment: A Genome‐Wide Interaction Meta‐Analysis in the International Consortium for Antihypertensive Pharmacogenomics Studies

Clinical Pharmacology & Therapeutics(2021)10.1002/cpt.2355

N/A

0DataRank · unranked

16 citations

Helen R. Warren, John Jack, Alison A. Motsinger‐Reif, Nicole D. Armstrong, Joshua C. Bis +23 more

Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies

UNC Libraries(2020)10.17615/tb6e-th27

N/A

0DataRank · unranked

0 citations

Christina L. Wassel, Tanja Zeller, Lina Zgaga, Eric Boerwinkle, Ben A. Oostra +95 more

Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations

Epigenetics(2024)10.1080/15592294.2024.2333668

N/A

0DataRank · unranked

9 citations

Ulrike Peters, Yao Hu, Farah Ammous, Christy L. Avery, Emelia J. Benjamin +35 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

Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans

UNC Libraries(2020)10.17615/y6gd-gc72

N/A

0DataRank · unranked

0 citations

Stacey Gabriel, Lisa Warsinger Martin, Deborah Farlow, Ethan M. Lange, Ramachandran S. Vasan +27 more

Fine-mapping, novel loci identification, and SNP association transferability in a genome-wide association study of QRS duration in African Americans

UNC Libraries(2020)10.17615/gng9-yn62

N/A

0DataRank · unranked

0 citations

Jonathan D. H. Smith, Steven Buyske, Erin N. Smith, Kathleen F. Kerr, Toshiko Tanaka +56 more

Sequencing of 2 Subclinical Atherosclerosis Candidate Regions in 3669 Individuals: Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing Study

UNC Libraries(2020)10.17615/wjqf-6y28

N/A

0DataRank · unranked

0 citations

Kari E. North, Donna M. Muzny, Xiaoming Liu, Joshua C. Bis, Eric Boerwinkle +10 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

Association analysis of mitochondrial DNA heteroplasmic variants: Methods and application

Mitochondrion(2024)10.1016/j.mito.2024.101954

N/A

0DataRank · unranked

2 citations

Katia Bulekova, Jian Yang, M M Lai, Achilleas Pitsillides, Xue Liu +19 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

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

Association analysis of mitochondrial DNA heteroplasmic variants: methods and application

medRxiv(2024)10.1101/2024.01.12.24301233

N/A

0DataRank · unranked

0 citations

Katia Bulekova, Jian Yang, M M Lai, Achilleas Pitsillides, Xue Liu +20 more

A system for phenotype harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) program

UNC Libraries(2024)10.17615/0ea7-3v47

N/A

0DataRank · unranked

0 citations

Nicola L. Hawley, May E. Montasser, P.A. Peyser, Daniel E. Weeks, Braxton D. Mitchell +67 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

N/A

0DataRank · unranked

0 citations

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

Determinants of mosaic chromosomal alteration fitness

UNC Libraries(2024)10.17615/yx5k-ka41

N/A

0DataRank · unranked

0 citations

Taralynn Mack, Margaret F. Doyle, Yash Pershad, Paul L. Auer, Jeong H. Yun +39 more

Genetic variants for head size share genes and pathways with cancer

UNC Libraries(2024)10.17615/0jt9-4n49

N/A

0DataRank · unranked

0 citations

Vince D. Calhoun, Manabu Nagata, Raymond A. Poot, Aad van der Lugt, Svenja Caspers +95 more

Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations

UNC Libraries(2024)10.17615/b6xd-h115

N/A

0DataRank · unranked

0 citations

Eimear E. Kenny, Chunyu Liu, Christy L. Avery, On Behalf of the PAGE Study, Nona Sotoodehnia +35 more

Prospective Associations of Coronary Heart Disease Loci in African Americans Using the MetaboChip: The PAGE Study

UNC Libraries(2020)10.17615/4xdt-j376

N/A

0DataRank · unranked

0 citations

Diane M. Becker, Nobuyo Maeda, Christopher J. O’Donnell, D. Y. Lin, Alex P. Reiner +26 more

Cholesteryl Ester Transfer Protein as a Drug Target for Cardiovascular Disease

Research Square(2020)10.21203/rs.3.rs-78818/v1

N/A

0DataRank · unranked

0 citations

Nicholas B. Hunt, María Gordillo‐Marañón, Pimphen Charoen, Fotios Drenos, Juan-Pablo Casas +19 more

Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskCLINICAL PERSPECTIVE

UNC Libraries(2020)10.17615/ttpw-sn86

N/A

0DataRank · unranked

0 citations

Alex P. Reiner, Donna M. Muzny, Shih‐Jen Hwang, Christopher Newton‐Cheh, Leslie J. Raffel +30 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

Association of exome sequences with plasma C-reactive protein levels in >9000 participants

UNC Libraries(2020)10.17615/003k-2b61

N/A

0DataRank · unranked

2 citations

Cristen J. Willer, Jennifer A. Brody, Eric Boerwinkle, Joshua C. Bis, Jeffery Haessler +27 more

Catechol‐O‐Methyltransferase Genotype, Frailty, and Gait Speed in a Biracial Cohort of Older Adults

Journal of the American Geriatrics Society(2020)10.1111/jgs.16842

N/A

0DataRank · unranked

6 citations

Andrea Rosso, Joshua C. Bis, Stephanie A. Studenski, Nico I. Bohnen, Caterina Rosano +1 more

Genomewide Association Studies of Stroke

UNC Libraries(2020)10.17615/xmdx-xm56

N/A

0DataRank · unranked

4 citations

Talin Haritunians, Shahar, Eyal, Peter J. Koudstaal, Kenneth Rice, Wayne D. Rosamond +27 more

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

Nature Methods(2025)10.1038/s41592-025-02919-5

N/A

0DataRank · unranked

0 citations

Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou +544 more

Whole genome sequence association analysis of brain structural volume measures in the NHLBI TOPMed Program highlights novel loci in diverse participants

10.1101/2025.06.11.25329426

N/A

0DataRank · unranked

0 citations

Mohsen Sharifitabar, Alexa Beiser, Claudia L. Satizábal, Thomas H. Mosley, Joanne E. Curran +34 more

Fibrinogen-Associated Plasma Metabolites and Implications for Coagulation, Inflammation, and Vascular Diseases

medRxiv(2025)10.1101/2025.08.06.25333064

N/A

0DataRank · unranked

0 citations

Taryn Alkis, Joshua C. Bis, Eric Boerwinkle, Jennifer A. Brody, Clary B. Clish +22 more

Adjustment for Genotype Imputation Uncertainty Corrects for Inflated Type I Error in Family‐Based Association Testing

Genetic Epidemiology(2025)10.1002/gepi.70021

N/A

0DataRank · unranked

0 citations

Joshua C. Bis, Nicola H. Chapman, Alejandro Q. Nato, Andréa R. V. R. Horimoto, Harkirat Sohi +5 more

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

EBioMedicine(2023)10.1016/j.ebiom.2023.104758

N/A

0DataRank · unranked

19 citations

Priyadarshini Kachroo, Tianxiao Huan, David Van Den Berg, Gha Young Lee, Helena Bui +95 more

Association of Severe Hypercholesterolemia and Familial Hypercholesterolemia Genotype With Risk of Coronary Heart Disease

Circulation(2023)10.1161/circulationaha.123.064168

N/A

0DataRank · unranked

12 citations

Jacqueline S. Dron, Brandon K. Bellows, Amit V. Khera, Junxiu Liu, Pallavi Balte +27 more

HLA-DP on Epithelial Cells Enables Tissue Damage by NKp44+ Natural Killer Cells in Ulcerative Colitis

Gastroenterology(2023)10.1053/j.gastro.2023.06.034

N/A

0DataRank · unranked

20 citations

Annika Niehrs, Frauke Degenhardt, Maria Schwerk, Ole Hinrichs, Ana Jordan-Paiz +94 more

Proteome Network Analysis Identifies Potential Biomarkers for Brain Aging

Journal of Alzheimer s Disease(2023)10.3233/jad-230145

N/A

0DataRank · unranked

5 citations

Alison E. Fohner, Håvard Kjesbu Skjellegrind, Alexa Beiser, Mitzi M. Gonzales, Claudia L. Satizábal +17 more

Serum NfL and GFAP are associated with incident dementia and dementia mortality in older adults: The cardiovascular health study

Alzheimer s & Dementia(2023)10.1002/alz.13367

N/A

0DataRank · unranked

48 citations

Xiaojuan Liu, Michelle C. Odden, Kristine F. Moseholm, Sudha Seshadri, Claudia L. Satizábal +10 more

Association of Peripheral Lymphocyte Subsets with Cognitive Decline and Dementia: The Cardiovascular Health Study

Journal of Alzheimer s Disease(2022)10.3233/jad-220091

N/A

0DataRank · unranked

5 citations

Colleen M. Sitlani, Petra Bůžková, Margaret F. Doyle, Xiaojuan Liu, Joshua C. Bis +16 more

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

UNC Libraries(2025)10.17615/mztm-gw84

N/A

0DataRank · unranked

0 citations

Margaret F. Doyle, Jason Bacon, Xiaolong Ma, Nathan Pankratz, Ramachandran S. Vasan +46 more

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

UNC Libraries(2025)10.17615/5tss-f273

N/A

0DataRank · unranked

0 citations

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

Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

Nature Communications(2023)10.1038/s41467-023-36192-x

Top 100%

0DataRank

Top 100%0 citations

Sonia Moreno–Grau, Niccoló Tesi, Benjamin Grenier‐Boley, Víctor Andrade, Iris E. Jansen +95 more

Joshua C. Bis

Indexed papers

Top data-sharing exemplar

Papers