Bogdan Paşaniuc

ORCID: 0000-0002-0227-2056

Also affiliated with California University of Pennsylvania, Translational Therapeutics (United States), University of Pennsylvania, Philadelphia University

Biochemistry, Genetics and Molecular BiologyMedicine

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

9.9Author DataRank

Indexed papers

5in 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 5 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.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Papers

Driven by 119 papers — median percentile 75. Top paper: “A structural variation reference for medical and population genetics”.

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

The contribution of rare variation to prostate cancer heritability

Nature Genetics(2015)10.1038/ng.3446

N/A

6.3DataRank · unranked

158 citations

Nicholas Mancuso, Kristin A. Rand, Arti Tandon, Alexander Allen, Swapan Mallick +20 more

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5

N/A

5.6DataRank · unranked

143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9

N/A

5.2DataRank · unranked

191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5

N/A

4.9DataRank · unranked

114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

Prior diagnoses and medications as risk factors for COVID-19 in a Los Angeles Health System

medRxiv(2020)10.1101/2020.07.03.20145581

N/A

2.4DataRank · unranked

55 citations

Yi Ding, Malika Freund, Ruth Johnson, Tommer Schwarz, Julie M. Yabu +8 more

Evaluating Performance and Agreement of Coronary Heart Disease Polygenic Risk Scores

JAMA(2024)10.1001/jama.2024.23784

N/A

1.9DataRank · unranked

60 citations

Kristin Boulier, Karl Keat, Katie M. Cardone, Manu Shivakumar, John DePaolo +35 more

Quantifying the contribution of dominance deviation effects to complex trait variation in biobank-scale data

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.03.018

N/A

1.4DataRank · unranked

45 citations

Alec Chiu, Kathryn S. Burch, Bogdan Paşaniuc, Sriram Sankararaman, Ali Pazokitoroudi

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7

N/A

1.4DataRank · unranked

9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 more

Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees

Proceedings of the National Academy of Sciences(2017)10.1073/pnas.1705859115

N/A

1.2DataRank · unranked

36 citations

Alisa Manning, Marcio Almeida, Matthew Zawistowski, Katharina Domschke, Tanya M. Teslovich +82 more

Best practices for multi-ancestry, meta-analytic transcriptome-wide association studies: Lessons from the Global Biobank Meta-analysis Initiative

Cell Genomics(2022)10.1016/j.xgen.2022.100180

N/A

1.1DataRank · unranked

40 citations

Jibril Hirbo, Dan Zhou, Wei Zhou, Jie Zheng, Masahiro Kanai +4 more

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 more

Large uncertainty in individual PRS estimation impacts PRS-based risk stratification

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.30.403188

N/A

0.955DataRank · unranked

11 citations

Kangcheng Hou, Kathryn S. Burch, Sandra Lapinska, Florian Privé, Bjarni J. Vilhjálmsson +3 more

The UCLA ATLAS Community Health Initiative: Promoting precision health research in a diverse biobank

Cell Genomics(2023)10.1016/j.xgen.2022.100243

Top 22%

0.928DataRank

Top 22%35 citations

Yi Ding, Arjun Bhattacharya, Sergey Knyazev, Alec Chiu, Clara Lajonchere +3 more

Principles and methods for transferring polygenic risk scores across global populations

Nature Reviews Genetics(2023)10.1038/s41576-023-00637-2

N/A

0.869DataRank · unranked

328 citations

Nilanjan Chatterjee, Jibril Hirbo, Daniel J. Schaid, Iman K. Martin, Iftikhar J. Kullo +12 more

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

Nature Genetics(2012)10.1038/ng.2283

N/A

0.868DataRank · unranked

326 citations

Nicholas Mancuso, Paul J. McLaren, Kiran Garimella, Noah Zaitlen, Alexandra P. Lewis +23 more

Genome-wide analyses characterize shared heritability among cancers and identify novel cancer susceptibility regions

JNCI Journal of the National Cancer Institute(2023)10.1093/jnci/djad043

Top 25%

0.804DataRank

Top 25%33 citations

Lu Wang, Helian Feng, Arunabha Majumdar, Sijia Huo, James W. MacDonald +56 more

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2

N/A

0.796DataRank · unranked

201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 more

Evaluating drug targets through human loss-of-function genetic variation

Nature(2020)10.1038/s41586-020-2267-z

N/A

0.779DataRank · unranked

179 citations

Konrad J. Karczewski, Hilary C. Martin, Beryl B. Cummings, Nicola Whiffin, Daniel R. Rhodes +150 more

Cross-ancestry atlas of gene, isoform, and splicing regulation in the developing human brain

Science(2024)10.1126/science.adh0829

Top 26%

0.765DataRank

Top 26%50 citations

Michael Margolis, Rujia Dai, Pan Zhang, Pawel F. Przytycki, Daniel Vo +95 more

Large-scale cross-cancer fine-mapping of the 5p15.33 region reveals multiple independent signals

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100041

Top 27%

0.739DataRank

Top 27%21 citations

Arunabha Majumdar, Lu Wang, Siddhartha Kar, Kevin M. Brown, Helian Feng +54 more

Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals

Nature Genetics(2023)10.1038/s41588-023-01338-6

N/A

0.727DataRank · unranked

126 citations

Yi Ding, Ziqi Xu, Yue Wu, Arjun Bhattacharya, Rachel Mester +24 more

Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.012

N/A

0.714DataRank · unranked

116 citations

Kathryn S. Burch, Ruth Johnson, Malika Freund, Gleb Kichaev, Nicholas Mancuso +4 more

Leveraging expression from multiple tissues using sparse canonical correlation analysis and aggregate tests improves the power of transcriptome-wide association studies

PLoS Genetics(2021)10.1371/journal.pgen.1008973

N/A

0.681DataRank · unranked

93 citations

Nicholas Mancuso, Alexander Gusev, Arunabha Majumdar, Megan Major, Bogdan Paşaniuc +2 more

Optimized design of single-cell RNA sequencing experiments for cell-type-specific eQTL analysis

Nature Communications(2020)10.1038/s41467-020-19365-w

N/A

0.635DataRank · unranked

68 citations

Tommer Schwarz, Arunabha Majumdar, Kangcheng Hou, Leah Briscoe, Richard K. Perez +7 more

Efficient variance components analysis across millions of genomes

Nature Communications(2020)10.1038/s41467-020-17576-9

N/A

0.624DataRank · unranked

63 citations

Yue Wu, Kathryn S. Burch, Kangcheng Hou, Aaron Zhou, Bogdan Paşaniuc +2 more

Temporally distinct 3D multi-omic dynamics in the developing human brain

Nature(2024)10.1038/s41586-024-08030-7

N/A

0.621DataRank · unranked

62 citations

Jingtian Zhou, Yi Zhang, Dong-Sung Lee, Kangcheng Hou, Oier Pastor-Alonso +25 more

Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

Genetic Epidemiology(2020)10.1002/gepi.22288

N/A

0.574DataRank · unranked

45 citations

Alexander Gusev, Bogdan Paşaniuc, Lang Wu, Jirong Long, Zomoroda Abu-Full +95 more

Fast estimation of genetic correlation for biobank-scale data

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.015

N/A

0.568DataRank · unranked

43 citations

Kathryn S. Burch, Andrea Ganna, Päivi Pajukanta, Bogdan Paşaniuc, Sriram Sankararaman +1 more

Impact of cross-ancestry genetic architecture on GWASs in admixed populations

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.001

N/A

0.546DataRank · unranked

37 citations

Kangcheng Hou, Yi Ding, Gillian Meeks, Kathryn S. Burch, Arjun Bhattacharya +3 more

Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery

Nature Medicine(2025)10.1038/s41591-025-03645-3

N/A

0.542DataRank · unranked

36 citations

Mattia Cordioli, Veronica Tozzo, Sarah Urbut, Kadri Arumäe, Roelof A. J. Smit +27 more

Genetically regulated multi-omics study for symptom clusters of posttraumatic stress disorder highlights pleiotropy with hematologic and cardio-metabolic traits

Molecular Psychiatry(2022)10.1038/s41380-022-01488-9

N/A

0.529DataRank · unranked

33 citations

Kritika Singh, Frank R. Wendt, Tyne W. Fleming, Cassie Overstreet, Dóra Koller +17 more

Splicing-specific transcriptome-wide association uncovers genetic mechanisms for schizophrenia

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.06.001

N/A

0.416DataRank · unranked

15 citations

Kofi Amoah, Jack Dodson, Mudra Choudhury, Arjun Bhattacharya, Giovanni Quinones-Valdez +3 more

Combining SNP-to-gene linking strategies to pinpoint disease genes and assess disease omnigenicity

medRxiv(2021)10.1101/2021.08.02.21261488

N/A

0.386DataRank · unranked

7 citations

Omer Weissbrod, Farhad Hormozdiari, Kushal K. Dey, Joseph Nasser, Karthik A. Jagadeesh +8 more

The contribution of rare variation to prostate cancer heritability

bioRxiv (Cold Spring Harbor Laboratory)(2015)10.1101/023440

N/A

0.365DataRank · unranked

5 citations

Kristin Rand, Arti Tandon, Alexander Allen, Swapan Mallick, Alexandra P. Lewis +20 more

Genotype error due to low-coverage sequencing induces uncertainty in polygenic scoring

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.015

N/A

0.330DataRank · unranked

8 citations

Yi Ding, Kangcheng Hou, Arjun Bhattacharya, Alexander Gusev, Noah Zaitlen +2 more

Exploring depression treatment response by using polygenic risk scoring across diverse populations

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.003

N/A

0.330DataRank · unranked

8 citations

Aditya Pimplaskar, Zhuozheng Shi, Yi Ding, Clara Frydman-Gani, Kangcheng Hou +5 more

Multi-ancestry polygenic risk scores for venous thromboembolism

Human Molecular Genetics(2024)10.1093/hmg/ddae097

N/A

0.292DataRank · unranked

6 citations

Florian Thibord, Alicia Domínguez Estirado, Corriene Sept, Kristin Boulier, Vidhya Venkateswaran +42 more

Calibrated prediction intervals for polygenic scores across diverse contexts

Research Square(2023)10.21203/rs.3.rs-3200692/v1

N/A

0.269DataRank · unranked

5 citations

Ziqi Xu, Yi Ding, Arbel Harpak, Bogdan Paşaniuc, Kangcheng Hou

Leveraging eQTLs to identify individual-level tissue of interest for a complex trait

PLoS Computational Biology(2021)10.1371/journal.pcbi.1008915

N/A

0.269DataRank · unranked

5 citations

Claudia Giambartolomei, Na Cai, Tanushree Haldar, Tommer Schwarz, Michael J. Gandal +3 more

Health care utilization of fine-scale identity by descent clusters in a Los Angeles biobank

medRxiv(2022)10.1101/2022.07.12.22277520

N/A

0.241DataRank · unranked

4 citations

Arya Boudaie, Ruhollah Shemirani, Ella Petter, Alec Chiu, Ruth Johnson +10 more

Leveraging expression from multiple tissues using sparse canonical correlation analysis and aggregate tests improve the power of transcriptome-wide association studies

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.03.186247

N/A

0.165DataRank · unranked

2 citations

Nicholas Mancuso, Alexander Gusev, Arunabha Majumdar, Megan Major, Bogdan Paşaniuc +2 more

Ancestry Calibration of Polygenic Risk Scores Improves Risk Stratification and Effect Estimation in African American Adults

medRxiv(2025)10.1101/2025.06.18.25329573

N/A

0.123DataRank · unranked

1 citations

Mariah Meyer, Iain R. Konigsberg, Aastha Kakar, Patrick M. Carry, Yun Li +14 more

Association between plausible genetic factors and weight loss from GLP1-RA and bariatric surgery: a multi-ancestry study in 10 960 individuals from 9 biobanks

medRxiv(2024)10.1101/2024.09.11.24313458

N/A

0.104DataRank · unranked

1 citations

Mattia Cordioli, Veronica Tozzo, Sarah Urbut, Kadri Arumäe, Roelof A. J. Smit +27 more

twas_sim, a Python-based tool for simulation and power analysis of transcriptome-wide association analysis

Bioinformatics(2023)10.1093/bioinformatics/btad288

N/A

0DataRank · unranked

6 citations

Zeyun Lu, Arjun Bhattacharya, Bogdan Paşaniuc, Nicholas Mancuso, Xinran Wang

Calibrated prediction intervals for polygenic scores across diverse contexts

medRxiv(2023)10.1101/2023.07.24.23293056

N/A

0DataRank · unranked

14 citations

Ziqi Xu, Yi Ding, Arbel Harpak, Bogdan Paşaniuc, Kangcheng Hou

Admix-kit: An Integrated Toolkit and Pipeline for Genetic Analyses of Admixed Populations

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.30.560263

N/A

0DataRank · unranked

9 citations

Stephanie M. Gogarten, Joohyun Kim, Xing Hua, Julie‐Alexia Dias, Quan Sun +10 more

Impact of cross-ancestry genetic architecture on GWAS in admixed populations

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.20.524946

N/A

0DataRank · unranked

7 citations

Kangcheng Hou, Yi Ding, Gillian Meeks, Kathryn S. Burch, Arjun Bhattacharya +3 more

Generalizability of PRS313 for breast cancer risk amongst non-Europeans in a Los Angeles biobank

arXiv (Cornell University)(2023)10.48550/arxiv.2305.03893

N/A

0DataRank · unranked

2 citations

Yi Ding, Vidhya Venkateswaran, Kristin Boulier, Nikhita Kathuria‐Prakash, Parisa Boodaghi Malidarreh +3 more

Cell type deconvolution of bulk blood RNA-Seq to reveal biological insights of neuropsychiatric disorders

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.24.542156

N/A

0DataRank · unranked

2 citations

Tommer Schwarz, Merel Bot, Kangcheng Hou, Christa Caggiano, Sandra Lapinska +7 more

Interplay Of Serum Bilirubin and Tobacco Smoking with Lung and Head and Neck Cancers in a Diverse, EHR-linked Los Angeles Biobank

medRxiv(2023)10.1101/2023.09.29.23296364

N/A

0DataRank · unranked

0 citations

Ella Petter, Kristin Boulier, Yi Ding, Arjun Bhattacharya, Bogdan Paşaniuc +1 more

Interplay Of Serum Bilirubin and Tobacco Smoking with Lung and Head and Neck Cancers in a Diverse, EHR-linked Los Angeles Biobank

Research Square(2023)10.21203/rs.3.rs-3471383/v1

N/A

0DataRank · unranked

0 citations

Ella Petter, Kristin Boulier, Yi Ding, Arjun Bhattacharya, Bogdan Paşaniuc +1 more

Calibrated prediction intervals for polygenic scores across diverse contexts

Nature Genetics(2024)10.1038/s41588-024-01792-w

N/A

0DataRank · unranked

59 citations

Ziqi Xu, Yi Ding, Ravi Mandla, Zhuozheng Shi, Kristin Boulier +3 more

Electronic health record signatures identify undiagnosed patients with common variable immunodeficiency disease

Science Translational Medicine(2024)10.1126/scitranslmed.ade4510

N/A

0DataRank · unranked

32 citations

Alexis V. Stephens, Rachel Mester, Sergey Knyazev, Lisa A. Kohn, Malika Freund +9 more

Admix-kit: an integrated toolkit and pipeline for genetic analyses of admixed populations

Bioinformatics(2024)10.1093/bioinformatics/btae148

N/A

0DataRank · unranked

16 citations

Stephanie M. Gogarten, Joohyun Kim, Xing Hua, Julie‐Alexia Dias, Quan Sun +89 more

Cell-type deconvolution of bulk-blood RNA-seq reveals biological insights into neuropsychiatric disorders

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2023.12.018

N/A

0DataRank · unranked

8 citations

Tommer Schwarz, Merel Bot, Kangcheng Hou, Christa Caggiano, Sandra Lapinska +7 more

Generalizability of PGS313 for breast cancer risk in a Los Angeles biobank

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100302

N/A

0DataRank · unranked

6 citations

Yi Ding, Vidhya Venkateswaran, Kristin Boulier, Nikhita Kathuria‐Prakash, Parisa Boodaghi Malidarreh +3 more

Improving genetic risk modeling of dementia from real-world data in underrepresented populations

Communications Biology(2024)10.1038/s42003-024-06742-0

N/A

0DataRank · unranked

3 citations

Leopoldo Valiente‐Banuet, Satpal S. Wadhwa, Bogdan Paşaniuc, Keith Vossel, Timothy S. Chang +1 more

Polygenic scores for tobacco use provide insights into systemic health risks in a diverse EHR-linked biobank in Los Angeles

Translational Psychiatry(2024)10.1038/s41398-024-02743-z

N/A

0DataRank · unranked

1 citations

Kristin Boulier, Yi Ding, Ruth Johnson, Arjun Bhattacharya, Bogdan Paşaniuc +1 more

Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction

medRxiv(2024)10.1101/2024.08.25.24312558

N/A

0DataRank · unranked

4 citations

Wenhan Lu, Yon Ho Jee, Ying Wang, Kristin Tsuo, David C. Qian +11 more

Multi-ancestry polygenic risk scores for venous thromboembolism

medRxiv(2024)10.1101/2024.01.09.24300914

N/A

0DataRank · unranked

2 citations

Florian Thibord, Alicia Domínguez Estirado, Corriene Sept, Kristin Boulier, Vidhya Venkateswaran +31 more

Multi-class Modeling Identifies Shared Genetic Risk for Late-onset Epilepsy and Alzheimer’s Disease

medRxiv(2024)10.1101/2024.02.05.24302353

N/A

0DataRank · unranked

2 citations

Thai Tran, Eleazar Eskin, Clara Lajonchere, Bogdan Paşaniuc, Daniel H. Geschwind +3 more

Improving genetic risk modeling of dementia from real-world data in underrepresented populations

medRxiv(2024)10.1101/2024.02.05.24302355

N/A

0DataRank · unranked

1 citations

Leopoldo Valiente‐Banuet, Satpal S. Wadhwa, UCLA Precision Health Data Discovery Repository Working Group, UCLA Precision Health ATLAS Working Group, Bogdan Paşaniuc +3 more

Isoform-level analyses of 6 cancers uncover extensive genetic risk mechanisms undetected at the gene-level

medRxiv(2024)10.1101/2024.10.29.24316388

N/A

0DataRank · unranked

1 citations

Sean T. Bresnahan, S. Taylor Head, Tabitha A. Harrison, Yao Yu, Chad D. Huff +4 more

Improving genetic risk modeling of dementia from real-world data in underrepresented populations

Research Square(2024)10.21203/rs.3.rs-3911508/v1

N/A

0DataRank · unranked

0 citations

Mingzhou Fu, Leopoldo Valiente‐Banuet, Satpal S. Wadhwa, Bogdan Paşaniuc, Keith Vossel +1 more

Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals

UNC Libraries(2024)10.17615/7x9d-na26

N/A

0DataRank · unranked

0 citations

Rachel Mester, David V. Conti, M. FORNAGE, S. Buyske, E.E. Kenny +24 more

Identifying common disease trajectories of Alzheimer’s disease with electronic health records

EBioMedicine(2025)10.1016/j.ebiom.2025.105831

N/A

0DataRank · unranked

5 citations

Sriram Sankararaman, Bogdan Paşaniuc, Keith Vossel, Timothy S. Chang, Mingzhou Fu

Proceedings of the second Artificial Intelligence in Primary Immunodeficiency (AIPI) meeting

Journal of Allergy and Clinical Immunology(2025)10.1016/j.jaci.2025.09.002

N/A

0DataRank · unranked

2 citations

Lisa Bastarache, Luiza C. Campos, Gerard Carot-Sans, Aaron Chin, Rumi Chunara +38 more

Isoform-level analyses of 6 cancers uncover extensive genetic risk mechanisms undetected at the gene-level

British Journal of Cancer(2025)10.1038/s41416-025-03141-y

N/A

0DataRank · unranked

1 citations

Sean T. Bresnahan, S. Taylor Head, Tabitha A. Harrison, Yao Yu, Chad D. Huff +4 more

PennPRS: a centralized cloud computing platform for efficient polygenic risk score training in precision medicine

medRxiv(2025)10.1101/2025.02.07.25321875

N/A

0DataRank · unranked

4 citations

Bingxuan Li, Xiyao Wang, Xiaochen Yang, Yujue Li, Ruofan Wang +10 more

Large-scale admixture mapping in the All of Us Research Program improves the characterization of cross-population phenotypic differences

medRxiv(2025)10.1101/2025.04.02.25325115

N/A

0DataRank · unranked

2 citations

Zhuozheng Shi, Kangcheng Hou, Ying Wang, Georgia Mies, Alan J. Aw +7 more

Inclusion bias affects common variant discovery and replication in a health-system linked biobank

medRxiv(2025)10.1101/2025.04.04.25325131

N/A

0DataRank · unranked

2 citations

Junqiong Qiu, Sandra Lapinska, Veronica Tozzo, Jeffrey N. Chiang, Bogdan Paşaniuc +2 more

Hidden structure in polygenic scores and the challenge of disentangling ancestry interactions in admixed populations

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.06.30.662316

N/A

0DataRank · unranked

1 citations

Ravi Mandla, Zhuozheng Shi, Penn Medicine BioBank, Bogdan Paşaniuc, Iain Mathieson +1 more

Multi-Trait Polygenic Scores for COPD and COPD Exacerbations Implicate Druggable Proteins

medRxiv(2025)10.1101/2025.08.22.25334001

N/A

0DataRank · unranked

0 citations

Iain R. Konigsberg, Yixuan He, Jingzhou Zhang, Tinashe Chikowore, William B. Feldman +22 more

Admix-kit: an integrated toolkit and pipeline for genetic analyses of admixed populations

UNC Libraries(2025)10.17615/6srp-f244

N/A

0DataRank · unranked

0 citations

Elizabeth G. Atkinson, Jibril Hirbo, Bogdan Paşaniuc, Stephanie M. Gogarten, Quan Sun +11 more

Multi-task learning identifies shared genetic risk for late-onset epilepsy and alzheimer’s disease

Scientific Reports(2025)10.1038/s41598-025-32329-8

N/A

0DataRank · unranked

0 citations

Thai Tran, Bogdan Paşaniuc, Keith Vossel, Timothy S. Chang, Mingzhou Fu

Challenges and Recommendations in Establishing National Human Diversity Genomic Projects

arXiv (Cornell University)(2025)10.48550/arxiv.2510.19869

N/A

0DataRank · unranked

0 citations

Walter Wolfsberger, Karishma Chhugani, Yu-Ning Huang, Valerii Pokrytiuk, Khrystyna Shchubelka +36 more

Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

UNC Libraries(2020)10.17615/haws-ma91

N/A

0DataRank · unranked

0 citations

Nicholas Mancuso, Paul J. McLaren, Kiran Garimella, Noah Zaitlen, Alexandra P. Lewis +19 more

Massively parallel reporter assays of melanoma risk variants identify MX2 as a gene promoting melanoma

Nature Communications(2020)10.1038/s41467-020-16590-1

N/A

0DataRank · unranked

144 citations

Tongwu Zhang, Andrew Vu, Julien Ablain, Matthew Makowski, Leandro M. Colli +22 more

Transcriptomic Insight Into the Polygenic Mechanisms Underlying Psychiatric Disorders

Biological Psychiatry(2020)10.1016/j.biopsych.2020.06.005

N/A

0DataRank · unranked

59 citations

Minsoo Kim, Gil D. Hoftman, Jillian R. Haney, Luis de la Torre-Ubieta, Bogdan Paşaniuc +2 more

A two-step approach to testing overall effect of gene–environment interaction for multiple phenotypes

Bioinformatics(2020)10.1093/bioinformatics/btaa1083

N/A

0DataRank · unranked

9 citations

Kathryn S. Burch, Tanushree Haldar, Sriram Sankararaman, Bogdan Paşaniuc, W. James Gauderman +2 more

Broad transcriptomic dysregulation across the cerebral cortex in ASD

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.17.423129

N/A

0DataRank · unranked

20 citations

Brie Wamsley, George Chen, Sepideh Parhami, Prashant S. Emani, Nathan Chang +17 more

Quantifying the contribution of dominance effects to complex trait variation in biobank-scale data

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.10.376897

N/A

0DataRank · unranked

7 citations

Alec Chiu, Kathryn S. Burch, Bogdan Paşaniuc, Sriram Sankararaman, Ali Pazokitoroudi

Credible learning of hydroxychloroquine and dexamethasone effects on COVID-19 mortality outside of randomized trials

medRxiv(2020)10.1101/2020.12.06.20244798

N/A

0DataRank · unranked

1 citations

David A. Wulf, Bogdan Paşaniuc, Onyebuchi A. Arah, Kristine M. Erlandson, Brian T. Montague +1 more

A scalable method for estimating the regional polygenicity of complex traits

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.15.908095

N/A

0DataRank · unranked

0 citations

Kathryn S. Burch, Kangcheng Hou, Mario Paciuc, Bogdan Paşaniuc, Sriram Sankararaman +1 more

Integrative approaches for large-scale transcriptome-wide association studies

UNC Libraries(2020)10.17615/q98d-fy71

N/A

0DataRank · unranked

0 citations

Marcus Alvarez, Fred A. Wright, Elina Nikkola, Huwenbo Shi, Patrick F. Sullivan +20 more

Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci

UNC Libraries(2020)10.17615/hx9s-wm59

N/A

0DataRank · unranked

0 citations

Devin Absher, Petra Bůžková, Wayne H.-H. Sheu, Wen‐Jane Lee, Ran Tao +52 more

Enhanced Statistical Tests for GWAS in Admixed Populations: Assessment using African Americans from CARe and a Breast Cancer Consortium

UNC Libraries(2020)10.17615/3jdw-6426

N/A

0DataRank · unranked

0 citations

Leslie A. Lange, Michael F. Press, Elisa V. Bandera, L. Adrienne Cupples, Solomon K. Musani +27 more

Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

UNC Libraries(2020)10.17615/vqrj-3e30

N/A

0DataRank · unranked

0 citations

Patrick F. Sullivan, Chongzhi Zang, David Collier, Hailiang Huang, Eli A. Stahl +24 more

Genome-wide Comparison of African-Ancestry Populations from CARe and Other Cohorts Reveals Signals of Natural Selection

UNC Libraries(2020)10.17615/hjj0-4367

N/A

0DataRank · unranked

0 citations

Pardis C. Sabeti, Leslie A. Lange, Josyf C. Mychaleckyj, George Papanicolaou, Noah Zaitlen +27 more

Reprogramming of the FOXA1 cistrome in treatment-emergent neuroendocrine prostate cancer

Nature Communications(2021)10.1038/s41467-021-22139-7

N/A

0DataRank · unranked

171 citations

David Y. Takeda, Ji-Heui Seo, Justin H. Hwang, Sheng-Yu Ku, Rand Arafeh +36 more

Large uncertainty in individual polygenic risk score estimation impacts PRS-based risk stratification

Nature Genetics(2021)10.1038/s41588-021-00961-5

N/A

0DataRank · unranked

153 citations

Kangcheng Hou, Kathryn S. Burch, Sandra Lapinska, Florian Privé, Bjarni J. Vilhjálmsson +3 more

Integrative genomic analyses identify susceptibility genes underlying COVID-19 hospitalization

Nature Communications(2021)10.1038/s41467-021-24824-z

N/A

0DataRank · unranked

81 citations

Kritika Singh, Tyne W. Miller‐Fleming, Frank R. Wendt, Nava Ehsan, Kangcheng Hou +10 more

H3K27ac HiChIP in prostate cell lines identifies risk genes for prostate cancer susceptibility

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.007

N/A

0DataRank · unranked

51 citations

Ji-Heui Seo, Tommer Schwarz, Malika Freund, Ruth Johnson, Sándor Spisák +6 more

Estimation of regional polygenicity from GWAS provides insights into the genetic architecture of complex traits

PLoS Computational Biology(2021)10.1371/journal.pcbi.1009483

N/A

0DataRank · unranked

25 citations

Kathryn S. Burch, Kangcheng Hou, Mario Paciuc, Bogdan Paşaniuc, Sriram Sankararaman +1 more

Pre-existing conditions in Hispanics/Latinxs that are COVID-19 risk factors

iScience(2021)10.1016/j.isci.2021.102188

N/A

0DataRank · unranked

19 citations

Yi Ding, Malika Freund, Ruth Johnson, Tommer Schwarz, Julie M. Yabu +34 more

Multitrait transcriptome‐wide association study (TWAS) tests

Genetic Epidemiology(2021)10.1002/gepi.22391

N/A

0DataRank · unranked

12 citations

Nicholas Mancuso, Bogdan Paşaniuc, Peter Kraft, Helian Feng

Polygenic enrichment distinguishes disease associations of individual cells in single-cell RNA-seq data

Research Square(2021)10.21203/rs.3.rs-933790/v1

N/A

0DataRank · unranked

28 citations

Kangcheng Hou, Bogdan Paşaniuc, Alkes L. Price, Kushal K. Dey, Karthik A. Jagadeesh +10 more

Best practices for multi-ancestry, meta-analytic transcriptome-wide association studies: lessons from the Global Biobank Meta-analysis Initiative

medRxiv(2021)10.1101/2021.11.24.21266825

N/A

0DataRank · unranked

11 citations

Jibril Hirbo, Dan Zhou, Wei Zhou, Jie Zheng, Masahiro Kanai +5 more

Polygenic enrichment distinguishes disease associations of individual cells in single-cell RNA-seq data

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.24.461597

N/A

0DataRank · unranked

4 citations

Kangcheng Hou, Kushal K. Dey, Saori Sakaue, Karthik A. Jagadeesh, Kathryn Weinand +10 more

Powerful eQTL mapping through low coverage RNA sequencing

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.08.455466

N/A

0DataRank · unranked

3 citations

Toni Boltz, Kangcheng Hou, Merel Bot, Chenda Duan, Loes M. Olde Loohuis +5 more

Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genes

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.17.456722

N/A

0DataRank · unranked

2 citations

Kangcheng Hou, Yi Ding, Yifei Wang, Steven Gazal, Huwenbo Shi +2 more

Broad transcriptomic dysregulation occurs across the cerebral cortex in ASD

Nature(2022)10.1038/s41586-022-05377-7

N/A

0DataRank · unranked

294 citations

Jillian R. Haney, Brie Wamsley, Chloe X. Yap, Sepideh Parhami, Prashant S. Emani +21 more

Polygenic enrichment distinguishes disease associations of individual cells in single-cell RNA-seq data

Nature Genetics(2022)10.1038/s41588-022-01167-z

N/A

0DataRank · unranked

278 citations

Kangcheng Hou, Kushal K. Dey, Saori Sakaue, Karthik A. Jagadeesh, Kathryn Weinand +10 more

Unlocking capacities of genomics for the COVID-19 response and future pandemics

Nature Methods(2022)10.1038/s41592-022-01444-z

N/A

0DataRank · unranked

67 citations

Karishma Chhugani, Varuni Sarwal, Ram Ayyala, Harman Singh, Smruthi Karthikeyan +30 more

Multi-ancestry fine-mapping improves precision to identify causal genes in transcriptome-wide association studies

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.07.002

N/A

0DataRank · unranked

63 citations

Shyamalika Gopalan, Yuan Dong, David V. Conti, Bogdan Paşaniuc, Alexander Gusev +2 more

Leveraging genomic diversity for discovery in an electronic health record linked biobank: the UCLA ATLAS Community Health Initiative

Genome Medicine(2022)10.1186/s13073-022-01106-x

N/A

0DataRank · unranked

51 citations

Yi Ding, Vidhya Venkateswaran, Arjun Bhattacharya, Kristin Boulier, Alec Chiu +21 more

Powerful eQTL mapping through low-coverage RNA sequencing

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100103

N/A

0DataRank · unranked

10 citations

Toni Boltz, Kangcheng Hou, Merel Bot, Chenda Duan, Loes M. Olde Loohuis +5 more

Polygenic scoring accuracy varies across the genetic ancestry continuum in all human populations

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.28.509988

N/A

0DataRank · unranked

17 citations

Kangcheng Hou, Ziqi Xu, Aditya Pimplaskar, Ella Petter, Kristin Boulier +5 more

Isoform-level transcriptome-wide association uncovers extensive novel genetic risk mechanisms for neuropsychiatric disorders in the human brain

medRxiv(2022)10.1101/2022.08.23.22279134

N/A

0DataRank · unranked

10 citations

Daniel Vo, Connor Jops, Minsoo Kim, Cindy Wen, Jonatan L. Hervoso +3 more

Multi-ancestry fine-mapping improves precision to identify causal genes in transcriptome-wide association studies

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.10.479993

N/A

0DataRank · unranked

6 citations

Shyamalika Gopalan, Yuan Dong, David V. Conti, Bogdan Paşaniuc, Alexander Gusev +2 more

Causal effects on complex traits are similar across segments of different continental ancestries within admixed individuals

medRxiv(2022)10.1101/2022.08.16.22278868

N/A

0DataRank · unranked

4 citations

Yi Ding, Ziqi Xu, Yue Wu, Arjun Bhattacharya, Rachel Mester +23 more

Causal effects on complex traits are similar across segments of different continental ancestries within admixed individuals

Research Square(2022)10.21203/rs.3.rs-1950966/v1

N/A

0DataRank · unranked

2 citations

Yi Ding, Ziqi Xu, Yue Wu, Arjun Bhattacharya, Rachel Mester +23 more

Distal gene regulation mediated by non-coding RNAs contributes to germline risk for breast and prostate cancer

medRxiv(2022)10.1101/2022.02.08.22270601

N/A

0DataRank · unranked

1 citations

Paige Lee, Tommer Schwarz, Pan Zhang, Matthew L. Freedman, Alexander Gusev +5 more

Electronic health record signatures identify undiagnosed patients with Common Variable Immunodeficiency Disease

medRxiv(2022)10.1101/2022.08.03.22278352

N/A

0DataRank · unranked

1 citations

Alexis V. Stephens, Sergey Knyazev, Lisa A. Kohn, Malika Freund, Leroy Bondhus +7 more

Germline determinants of the prostate tumor genome

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.11.16.516773

N/A

0DataRank · unranked

0 citations

Jiapei Yuan, Tommer Schwarz, Julie Livingstone, Natalie S. Fox, Weerachai Jaratlerdsiri +36 more

Polygenic scoring accuracy varies across the genetic ancestry continuum

Nature(2023)10.1038/s41586-023-06079-4

N/A

0DataRank · unranked

323 citations

Kangcheng Hou, Ziqi Xu, Aditya Pimplaskar, Ella Petter, Kristin Boulier +5 more

Isoform-level transcriptome-wide association uncovers genetic risk mechanisms for neuropsychiatric disorders in the human brain

Nature Genetics(2023)10.1038/s41588-023-01560-2

N/A

0DataRank · unranked

62 citations

Daniel Vo, Connor Jops, Minsoo Kim, Cindy Wen, Jonatan L. Hervoso +3 more

Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region

Nature Medicine(2023)10.1038/s41591-023-02425-1

N/A

0DataRank · unranked

14 citations

Arya Boudaie, Ruhollah Shemirani, Joel Mefford, Ella Petter, Alec Chiu +14 more

Bogdan Paşaniuc

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