Mark Kvale

4.1k total citations
27 papers, 990 citations indexed

About

Mark Kvale is a scholar working on Genetics, Molecular Biology and Ophthalmology. According to data from OpenAlex, Mark Kvale has authored 27 papers receiving a total of 990 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 5 papers in Molecular Biology and 5 papers in Ophthalmology. Recurrent topics in Mark Kvale's work include Genetic Associations and Epidemiology (9 papers), Genomics and Rare Diseases (6 papers) and Retinal Diseases and Treatments (4 papers). Mark Kvale is often cited by papers focused on Genetic Associations and Epidemiology (9 papers), Genomics and Rare Diseases (6 papers) and Retinal Diseases and Treatments (4 papers). Mark Kvale collaborates with scholars based in United States, India and United Kingdom. Mark Kvale's co-authors include Neil Risch, Catherine Schaefer, Eric Jorgenson, Thomas J. Hoffmann, Christoph E. Schreiner, Yambazi Banda, Hélène Choquet, Pui–Yan Kwok, Jie Yin and Ofer Biham and has published in prestigious journals such as Nature Communications, Nature Genetics and Journal of Neurophysiology.

In The Last Decade

Mark Kvale

27 papers receiving 977 citations

Peers

Countries citing papers authored by Mark Kvale

Since Specialization

Citations

This map shows the geographic impact of Mark Kvale's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Mark Kvale with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark Kvale more than expected).

Fields of papers citing papers by Mark Kvale

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark Kvale. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Mark Kvale. The network helps show where Mark Kvale may publish in the future.

Co-authorship network of co-authors of Mark Kvale

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Kvale. A scholar is included among the top collaborators of Mark Kvale based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Mark Kvale. Mark Kvale is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	SLCO1B1 Functional Variants, Bilirubin, Statin‐Induced Myotoxicity, and Recent Sub‐Saharan African Ancestry: A Precision Medicine Health Equity Study 2025 ·Clinical Pharmacology & Therapeutics ·Tanushree Haldar, Mark Kvale, Jia Yang, Michael P. Douglas, Willow Coyote‐Maestas, Linda Kachuri, John S. Witte, Carlos Iribarren, Marisa W. Medina, Ronald M. Krauss, Sook Wah Yee, Akinyemi Oni‐Orisan	3
2	Genetic ancestry and diagnostic yield of exome sequencing in a diverse population 2024 ·npj Genomic Medicine ·(unknown), Nuriye Sahin‐Hodoglugil, Uğur Hodoğlugil, Mark Kvale, Pierre‐Marie Martin, Jessica Van Ziffle, W. Patrick Devine, Sara Ackerman, Barbara A. Koenig, Pui–Yan Kwok, Mary E. Norton, Anne Slavotinek, Neil Risch	7
3	Risk factors for inguinal hernia repair among US adults 2023 ·Hernia ·(unknown), Mark Kvale, Jie Yin, Sanjay R. Patel, Eric Jorgenson, Rouzbeh Mostaedi, Hélène Choquet	5
4	Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience 2022 ·Human Genetics and Genomics Advances ·(unknown), Laura M. Amendola, Tia L. Kauffman, Kathleen F. Mittendorf, Jeannette T. Bensen, Flavia Chen, Richard Green, Bradford C. Powell, Mark Kvale, Frank Angelo, Laura Farnan, Stephanie M. Fullerton, Jill O. Robinson, Tianran Li, (unknown), James M.J. Lawlor, Jeffrey Ou, Lucia A. Hindorff, Gail P. Jarvik, David R. Crosslin	6
5	Predicting genes from phenotypes using human phenotype ontology (HPO) terms 2022 ·Human Genetics ·Anne Slavotinek, Hannah Prasad, (unknown), Shannon Rego, (unknown), Mark Kvale	4
6	A multiethnic genome-wide analysis of 44,039 individuals identifies 41 new loci associated with central corneal thickness 2020 ·Communications Biology ·Hélène Choquet, Ronald B. Melles, Jie Yin, Thomas J. Hoffmann, Khanh K. Thai, Mark Kvale, Yambazi Banda, Alison J. Hardcastle, Stephen J. Tuft, M. Maria Glymour, Catherine Schaefer, Neil Risch, K. Saidas Nair, Pirro G. Hysi, Eric Jorgenson	26
7	Genetic ancestry, skin pigmentation, and the risk of cutaneous squamous cell carcinoma in Hispanic/Latino and non-Hispanic white populations 2020 ·Communications Biology ·Eric Jorgenson, Hélène Choquet, Jie Yin, Thomas J. Hoffmann, Yambazi Banda, Mark Kvale, Neil Risch, Catherine Schaefer, Maryam M. Asgari	6
8	Telomere length and socioeconomic status at neighborhood and individual levels among 80,000 adults in the Genetic Epidemiology Research on Adult Health and Aging cohort 2019 ·Environmental Epidemiology ·Stacey Alexeeff, Catherine Schaefer, Mark Kvale, Jun Shan, Elizabeth H. Blackburn, Neil Risch, Dilrini K. Ranatunga, Eric Jorgenson, Thomas J. Hoffmann, Lori C. Sakoda, Charles P. Quesenberry, Stephen K. Van Den Eeden	28
9	A large electronic-health-record-based genome-wide study of serum lipids 2018 ·Nature Genetics ·Thomas J. Hoffmann, Elizabeth Theusch, Tanushree Haldar, Dilrini K. Ranatunga, Eric Jorgenson, Marisa W. Medina, Mark Kvale, Pui–Yan Kwok, Catherine Schaefer, Ronald M. Krauss, Carlos Iribarren, Neil Risch	170
10	A multiethnic genome-wide association study of primary open-angle glaucoma identifies novel risk loci 2018 ·Nature Communications ·Hélène Choquet, (unknown), Stephen C. Kneeland, Khanh K. Thai, Thomas J. Hoffmann, Jie Yin, Mark Kvale, Yambazi Banda, Nicholas Tolman, Pete A. Williams, Catherine Schaefer, Ronald B. Melles, Neil Risch, Simon W. M. John, K. Saidas Nair, Eric Jorgenson	104
11	A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci 2018 ·Genetics ·Thomas J. Hoffmann, Hélène Choquet, Jie Yin, Yambazi Banda, Mark Kvale, M. Maria Glymour, Catherine Schaefer, Neil Risch, Eric Jorgenson	118
12	Pierpont syndrome associated with the p.Tyr446Cys missense mutation in TBL1XR1 2017 ·European Journal of Medical Genetics ·Anne Slavotinek, Heather H. Pua, Uğur Hodoğlugil, Jude Abadie, Joseph T.C. Shieh, Jessica Van Ziffle, Mark Kvale, Hane Lee, Pui–Yan Kwok, Neil Risch, M.G. Sabbadini	16
13	A large multi-ethnic genome-wide association study identifies novel genetic loci for intraocular pressure 2017 ·Nature Communications ·Hélène Choquet, Khanh K. Thai, Jie Yin, Thomas J. Hoffmann, Mark Kvale, Yambazi Banda, Catherine Schaefer, Neil Risch, K. Saidas Nair, Ronald B. Melles, Eric Jorgenson	63
14	Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study 2017 ·Molecular Psychiatry ·Eric Jorgenson, Khanh K. Thai, Thomas J. Hoffmann, Lori C. Sakoda, Mark Kvale, Yambazi Banda, Cathy Schaefer, Neil Risch, Jennifer R. Mertens, Constance Weisner, Hélène Choquet	95
15	Common coding variants in the HLA-DQB1 region confer susceptibility to age-related macular degeneration 2016 ·European Journal of Human Genetics ·Eric Jorgenson, Ronald B. Melles, Thomas J. Hoffmann, Xiaoming Jia, Lori C. Sakoda, Mark Kvale, Yambazi Banda, Catherine Schaefer, Neil Risch, Ling Shen	11
16	Imputation of the Rare HOXB13 G84E Mutation and Cancer Risk in a Large Population-Based Cohort 2015 ·PLoS Genetics ·Thomas J. Hoffmann, Lori C. Sakoda, Ling Shen, Eric Jorgenson, Laurel A. Habel, Jinghua Liu, Mark Kvale, Maryam M. Asgari, Yambazi Banda, Douglas A. Corley, Lawrence H. Kushi, Charles P. Quesenberry, Catherine Schaefer, Stephen K. Van Den Eeden, Neil Risch, John S. Witte	25
17	Estimating genotype error rates from high-coverage next-generation sequence data 2014 ·Genome Research ·Jeffrey D. Wall, Ling Tang, (unknown), Mark Kvale, Pui–Yan Kwok, Catherine Schaefer, Neil Risch	87
18	B4-4: Genome-Wide Association Study of Macular Degeneration: Early Results from the Kaiser Permanente Research Program on Genes, Environment, and Health (RPGEH) 2013 ·Clinical Medicine & Research ·Eric Jorgenson, Stanley Sciortino, Ling Shen, Dilrini K. Ranatunga, Thomas J. Hoffmann, Mark Kvale, (unknown), Pui–Yan Kwok, Lutz Walter, Neil Risch, Catherine Schaefer	2
19	VALID: visualization of association study results and linkage disequilibrium 2009 ·Genetic Epidemiology ·Eric Jorgenson, Mark Kvale, John S. Witte	2
20	Segmentation and Estimation for SNP Microarrays: A Bayesian Multiple Change‐Point Approach 2009 ·Biometrics ·Yu Chuan Tai, Mark Kvale, John S. Witte	5

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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