Pui–Yan Kwok

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

9.3Author 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.

Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese

npj Genomic Medicine(2021)10.1038/s41525-021-00178-9

Top 4%

5.0DataRank

Top 4%272 citations

Jenn-Hwai Yang, Erh‐Chan Yeh, Ming-Fang Tsai, Hsiao‐Jung Kao, Chen-Zen Lo +16 more

Papers

Driven by 28 papers — median percentile 85. Top paper: “Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese”.

Genetic profiles of 103,106 individuals in the Taiwan Biobank provide insights into the health and history of Han Chinese

npj Genomic Medicine(2021)10.1038/s41525-021-00178-9

Top 4%

5.0DataRank

Top 4%272 citations

Jenn-Hwai Yang, Erh‐Chan Yeh, Ming-Fang Tsai, Hsiao‐Jung Kao, Chen-Zen Lo +16 more

Towards a reference genome that captures global genetic diversity

Nature Communications(2020)10.1038/s41467-020-19311-w

Top 12%

1.8DataRank

Top 12%64 citations

Walfred Ma, Chun-Yu Wei, Erh‐Chan Yeh, Wan-Jia Lin, Elin H. F. Wang +19 more

Comprehensive Analysis of Human Subtelomeres by Whole Genome Mapping

PLoS Genetics(2020)10.1371/journal.pgen.1008347

Top 15%

1.4DataRank

Top 15%58 citations

Heba Z. Abid, Pui–Yan Kwok, Harold Riethman, Ming Xiao, Eleanor Young

Accurate assembly of the olive baboon ( Papio anubis ) genome using long-read and Hi-C data

GigaScience(2020)10.1093/gigascience/giaa134

Top 19%

1.1DataRank

Top 19%39 citations

Michal Levy‐Sakin, Jacqueline A. Robinson, Joseph Guillory, Steffen Durinck, Tauras P. Vilgalys +6 more

Loss-of-function mutations in Notch receptors in cutaneous and lung squamous cell carcinoma

Proceedings of the National Academy of Sciences(2011)10.1073/pnas.1114669108

N/A

0.923DataRank · unranked

468 citations

Zachary Sanborn, Kelly L. Arnett, Laura J. Bayston, Wilson Liao, Charlotte M. Proby +33 more

The role of exome sequencing in newborn screening for inborn errors of metabolism

Nature Medicine(2020)10.1038/s41591-020-0966-5

N/A

0.835DataRank · unranked

261 citations

Renata C. Gallagher, Yaqiong Wang, Robert J. Currier, George S. Amatuni, Laia Bassaganyas +19 more

Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder

Molecular Psychiatry(2021)10.1038/s41380-020-01006-9

N/A

0.686DataRank · unranked

22 citations

Fernando S. Goes, Adam E. Locke, Duncan S. Palmer, Weiqing Wang, Sarah Cohen‐Woods +71 more

Application of full-genome analysis to diagnose rare monogenic disorders

npj Genomic Medicine(2021)10.1038/s41525-021-00241-5

N/A

0.598DataRank · unranked

53 citations

Monica Penon‐Portmann, K. Wong, Michal Levy‐Sakin, Michelle Verghese, Anne Slavotinek +15 more

Diagnostic yield of pediatric and prenatal exome sequencing in a diverse population

npj Genomic Medicine(2023)10.1038/s41525-023-00353-0

N/A

0.568DataRank · unranked

43 citations

Shannon Rego, Nuriye Sahin‐Hodoglugil, Mark Kvale, Billie R. Lianoglou, Tiffany Yip +33 more

Genome mapping resolves structural variation within segmental duplications associated with microdeletion/microduplication syndromes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.30.071449

N/A

0DataRank · unranked

2 citations

Feyza Yilmaz, Stephen K. Chow, Catherine Chu, Chin Jia Lin, Elizabeth A. Geiger +6 more

DNA from dried blood spots yields high quality sequences for exome analysis

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.19.105304

N/A

0DataRank · unranked

2 citations

Aashish N. Adhikari, Kunal Kundu, Jennifer M. Puck, Robert J. Currier, Pui–Yan Kwok +3 more

Perturbation robustness analyses reveal important parameters in variant interpretation pipelines

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.29.173815

N/A

0DataRank · unranked

2 citations

Aashish N. Adhikari, Uma Sunderam, Mark Kvale, Robert J. Currier, Renata C. Gallagher +5 more

Newborn Sequencing in Genomic Medicine and Public Health

UNC Libraries(2020)10.17615/p3y4-3s09

N/A

0DataRank · unranked

0 citations

Stacey Pereira, Sean D. Mooney, Anastasia L. Wise, Jennifer M. Puck, Timothy W. Yu +37 more

Inflammation and stress-related candidate genes, plasma interleukin-6 levels, and longevity in older adults

UNC Libraries(2020)10.17615/aycf-t384

N/A

0DataRank · unranked

0 citations

Andrea Z. LaCroix, Pui–Yan Kwok, Amy M. Matteini, Nir Barzilai, Gil Atzmon +11 more

Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann‐Steiner syndrome

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62124

N/A

0DataRank · unranked

72 citations

Ian M. Campbell, Margaret Harr, Nina B. Gold, Dong Li, Hans T. Björnsson +95 more

Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation

Genetics(2021)10.1093/genetics/iyaa038

N/A

0DataRank · unranked

20 citations

Feyza Yilmaz, Stephen K. Chow, Catherine Chu, Chin Jia Lin, Elizabeth A. Geiger +7 more

Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner Syndrome

Molecular Genetics and Metabolism(2021)10.1016/s1096-7192(21)00373-5

N/A

0DataRank · unranked

1 citations

Ian M. Campbell, Margaret Harr, Nina B. Gold, Dong Li, Hans T. Björnsson +95 more

Multi-modal investigation of the schizophrenia-associated 3q29 genomic interval reveals global genetic diversity with unique haplotypes and segments that increase the risk for non-allelic homologous recombination

medRxiv(2021)10.1101/2021.11.10.21266197

N/A

0DataRank · unranked

2 citations

Gurusamy Umamaheswaran, Trenell J. Mosley, Yulia Mostovoy, Tamim H. Shaikh, Michael E. Zwick +4 more

Whole-exome sequencing reveals damaging gene variants associated with hypoalphalipoproteinemia

Journal of Lipid Research(2022)10.1016/j.jlr.2022.100209

N/A

0DataRank · unranked

8 citations

K. Wong, Youbin Liu, Michal Levy‐Sakin, Wei‐Chien Hung, Mo Li +17 more

High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing

Genome Medicine(2023)10.1186/s13073-023-01184-5

N/A

0DataRank · unranked

11 citations

Gurusamy Umamaheswaran, Trenell J. Mosley, Pille Hallast, Kwondo Kim, Yulia Mostovoy +7 more

Data from A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility

(2023)10.1158/0008-5472.c.6513064

Top 100%

0DataRank

Top 100%0 citations

Taylor B. Cavazos, Sara R. Rashkin, Clinton L. Cario, Rebecca E. Graff, Caroline G. Tai +21 more

Diagnostic Yield of Exome Sequencing in a Diverse Pediatric and Prenatal Population is not Associated with Genetic Ancestry

medRxiv(2023)10.1101/2023.05.19.23290066

N/A

0DataRank · unranked

0 citations

Nuriye Sahin‐Hodoglugil, Uğur Hodoğlugil, Mark Kvale, Pierre‐Marie Martin, Jessica Van Ziffle +8 more

Genetic ancestry and diagnostic yield of exome sequencing in a diverse population

npj Genomic Medicine(2024)10.1038/s41525-023-00385-6

N/A

0DataRank · unranked

19 citations

Nuriye Sahin‐Hodoglugil, Uğur Hodoğlugil, Mark Kvale, Pierre‐Marie Martin, Jessica Van Ziffle +8 more

Analysis of putative cis-regulatory elements regulating blood pressure variation

Human Molecular Genetics(2020)10.1093/hmg/ddaa098

N/A

0DataRank · unranked

13 citations

Dongwon Lee, Thomas J. Hoffmann, Georg Ehret, Dan E. Arking, Dilrini K. Ranatunga +9 more

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

Science(2025)10.1126/science.adp4753

N/A

0DataRank · unranked

48 citations

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

Genomic Analysis of Historical Cases with Positive Newborn Screens for Short-Chain Acyl-CoA Dehydrogenase Deficiency Shows That a Validated Second-Tier Biochemical Test Can Replace Future Sequencing

International Journal of Neonatal Screening(2020)10.3390/ijns6020041

N/A

0DataRank · unranked

19 citations

Robert J. Currier, Hao Tang, Coleman Turgeon, Robert L. Nussbaum, Rajgopal Srinivasan +7 more

A Large-Scale Association Study Detects Novel Rare Variants, Risk Genes, Functional Elements, and Polygenic Architecture of Prostate Cancer Susceptibility

Cancer Research(2020)10.1158/0008-5472.can-20-2635

N/A

0DataRank · unranked

25 citations

Taylor B. Cavazos, Sara R. Rashkin, Clinton L. Cario, Rebecca E. Graff, Caroline G. Tai +21 more

Application of Full Genome Analysis to Diagnose Rare Monogenic Disorders

medRxiv(2020)10.1101/2020.10.22.20216531

N/A

0DataRank · unranked

9 citations

Monica Penon‐Portmann, K. Wong, Michal Levy‐Sakin, Michelle Verghese, Anne Slavotinek +15 more

Pui–Yan Kwok

Indexed papers

Top data-sharing exemplar

Papers