Lucia A. Hindorff

43.0k citations

64 papers · 8.5k indexed · 3 hit papers · h-index 30

Genetics top 0.2%
- Genetic Associations and Epidemiology 17
- Genomics and Rare Diseases 16
- BRCA gene mutations in cancer 11
Cancer Research top 2%
- Cancer Genomics and Diagnostics 5
Molecular Biology top 1%
- Bioinformatics and Genomic Networks 6
Aging top 5%
Endocrinology, Diabetes and Metabolism top 2%
- Hormonal Regulation and Hypertension 8
Public Health, Environmental and Occupational Health
- Ethics in Clinical Research 12
Hematology
- Blood Coagulation and Thrombosis Mechanisms 7

Co-authors: Heather Junkins Teri A. Manolio Erin M. Ramos Praveen Sethupathy Francis S. Collins Jacqueline A. L. MacArthur Helen Parkinson Peggy Hall
Cited by: Genetics Cancer Research Molecular Biology
Journals: Genetics in Medicine (7 papers)European Journal of Human Genetics (3 papers)American Journal of Hypertension (3 papers)
Partner nations: United States United Kingdom Netherlands

In The Last Decade

Lucia A. Hindorff

61 papers receiving 8.4k citations

Hit Papers

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What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

2016 Nucleic Acids Research
2013 Nucleic Acids Research
2009 Proceedings of the National Academy of Sciences

Peers

Countries citing papers authored by Lucia A. Hindorff

Since Specialization

Citations

This map shows the geographic impact of Lucia A. Hindorff'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 Lucia A. Hindorff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lucia A. Hindorff more than expected).

Fields of papers citing papers by Lucia A. Hindorff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lucia A. Hindorff. 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 Lucia A. Hindorff. The network helps show where Lucia A. Hindorff may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Lucia A. Hindorff, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Lucia A. Hindorff Line = papers co-authored together Lucia A. Hindorff links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	The motivation and process for developing a consortium‐wide time and motion study to estimate resource implications of innovations in the use of genome sequencing to inform patient care Clinical and Translational Science ·P. Bernard,Dirk Van Rooyan,王有航,Jeannette T. Bensen,M. Carme,Candice R. Finnila,Lucia A. Hindorff,Y. Li,Frances L. Lynch,Kamalpreet Rakhra,Hadley Stevens Smith,Melissa Wasserstein,Kristen Hassmiller Lich	2023	0
2	Lessons learned and recommendations for data coordination in collaborative research: The CSER consortium experience Human Genetics and Genomics Advances ·Lee Seow Kheng,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,Сотниченко Александр Анатольевич,James M.J. Lawlor,Jeffrey Ou,Lucia A. Hindorff,Gail P. Jarvik,David R. Crosslin	2022	6
3	Cost-effectiveness frameworks for comparing genome and exome sequencing versus conventional diagnostic pathways: A scoping review and recommended methods Genetics in Medicine ·Bart S. Ferket,장규인,Сотниченко Александр Анатольевич,Akila Pai,Kathleen F. Mittendorf,Heidi V. Russell,Flavia Chen,Frances L. Lynch,Kristen Hassmiller Lich,Lucia A. Hindorff,Renate Savich,Anne Slavotinek,Hadley Stevens Smith,Bruce D. Gelb,David L. Veenstra	2022	9
4	Sequencing-based genome-wide association studies reporting standards Cell Genomics ·Aoife McMahon,Elizabeth Lewis,Annalisa Buniello,María Cerezo,Peggy Hall,Elliot Sollis,Helen Parkinson,Lucia A. Hindorff,Laura W. Harris,Jacqueline A. L. MacArthur	2021	10
5	US private payers’ perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER) Genetics in Medicine ·Kathryn A. Phillips,Julia R. Trosman,Michael P. Douglas,Bruce D. Gelb,Bart S. Ferket,Lucia A. Hindorff,Anne Slavotinek,Jonathan S. Berg,Heidi V. Russell,Beth Devine,Sinian Li,Hadley Stevens Smith	2021	8
6	Alaska Native genomic research: perspectives from Alaska Native leaders, federal staff, and biomedical researchers Genetics in Medicine ·Vanessa Y. Hiratsuka,Michael Hahn,R. Brian Woodbury,Sara Chandros Hull,David R. Wilson,Vence L. Bonham,Denise A. Dillard,Jaedon P. Avey,Andrea Beckel‐Mitchener,Juliana Blome,Katrina G. Claw,Elizabeth D. Ferucci,Francine C. Gachupin,Armen A. Ghazarian,Lucia A. Hindorff,Sheena Gingerich,Susan Brown Trinidad,Jennifer L. Troyer,Kelly Bynum,Sheena Gingerich,Kelly Bynum	2020	17
7	Clinical Genetics Lacks Standard Definitions and Protocols for the Collection and Use of Diversity Measures The American Journal of Human Genetics ·Alice B. Popejoy,Kristy Crooks,Stephanie M. Fullerton,Lucia A. Hindorff,Gillian W. Hooker,Barbara A. Koenig,Manuel Loeber,Erin M. Ramos,Deborah Ritter,Hannah Wand,Matt W. Wright,Michael Yudell,James Zou,Sharon E. Plon,Carlos D. Bustamante,Kelly E. Ormond	2020	50
8	Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings Genetics in Medicine ·Kurt D. Christensen,Barbara A. Bernhardt,Gail P. Jarvik,Lucia A. Hindorff,Jeffrey Ou,Sawona Biswas,Bradford C. Powell,Robert W. Grundmeier,Kalotina Machini,Dean Karavite,Jeffrey W. Pennington,Ian D. Krantz,Jonathan S. Berg,Katrina A.B. Goddard	2018	5
9	The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)breakdown → Nucleic Acids Research ·Jacqueline A. L. MacArthur,Emily Bowler-Barnett,María Cerezo,Laurent Gil,Peggy Hall,Emma Hastings,Heather Junkins,Aoife McMahon,Annalisa Milano,Joannella Morales,Zoë May Pendlington,Danielle Welter,Tony Burdett,Lucia A. Hindorff,Paul Flicek,Fiona Cunningham,Helen Parkinson	2016	1346
10	A survey of informatics approaches to whole-exome and whole-genome clinical reporting in the electronic health record Genetics in Medicine ·Peter Tarczy‐Hornoch,Laura M. Amendola,Samuel Aronson,Levi A. Garraway,Stacy W. Gray,Robert W. Grundmeier,Lucia A. Hindorff,Gail P. Jarvik,Dean Karavite,Matthew S. Lebo,Sharon E. Plon,Eliezer M. Van Allen,Karen E. Weck,Peter S. White,Yaping Yang	2013	49
11	The NHGRI GWAS Catalog, a curated resource of SNP-trait associationsbreakdown → Nucleic Acids Research ·Danielle Welter,Jacqueline A. L. MacArthur,Joannella Morales,Tony Burdett,Peggy Hall,Heather Junkins,Olufunke Ogunmoroti,Paul Flicek,Teri A. Manolio,Lucia A. Hindorff,Helen Parkinson	2013	1850
12	A Phenomics-Based Strategy Identifies Loci on APOC1, BRAP, and PLCG1 Associated with Metabolic Syndrome Phenotype Domains PLoS Genetics ·Christy L. Avery,Qianchuan He,Kari E. North,José Luis Ambite,Eric Boerwinkle,Myriam Fornage,Lucia A. Hindorff,Charles Kooperberg,James B. Meigs,James S. Pankow,Sarah A. Pendergrass,Bruce M. Psaty,Marylyn D. Ritchie,Jerome I. Rotter,Kent D. Taylor,Lynne R. Wilkens,Gerardo Heiss,Dan Lin	2011	77
13	Genetic architecture of cancer and other complex diseases: lessons learned and future directions Carcinogenesis ·Lucia A. Hindorff,Elizabeth M. Gillanders,Teri A. Manolio	2011	75
14	Potential etiologic and functional implications of genome-wide association loci for human diseases and traitsbreakdown → Proceedings of the National Academy of Sciences ·Lucia A. Hindorff,Praveen Sethupathy,Heather Junkins,Erin M. Ramos,Yash Wasule,Francis S. Collins,Teri A. Manolio	2009	2820
15	Motivating Factors for Physician Ordering of Factor V Leiden Genetic Tests Archives of Internal Medicine ·Lucia A. Hindorff,Wylie Burke,Omar Luis Hernández García,Kenneth Rice,Thomas Lumley,Kathleen A. Leppig,Frits R. Rosendaal,Eric B. Larson,Bruce M. Psaty	2009	16
16	Common variation in cytochrome P450 epoxygenase genes and the risk of incident nonfatal myocardial infarction and ischemic stroke Pharmacogenetics and Genomics ·Kristin D. Marciante,Rheem A. Totah,Susan R. Heckbert,Nicholas L. Smith,Rozenn N. Lemaître,Thomas Lumley,Kenneth Rice,Lucia A. Hindorff,Joshua C. Bis,H. Lombaerts,Bruce M. Psaty	2008	48
17	Common variants in the CRP gene in relation to longevity and cause-specific mortality in older adults: The Cardiovascular Health Study Atherosclerosis ·Lucia A. Hindorff,Kenneth Rice,Leslie A. Lange,Paula Diehr,Indrani Halder,Jeremy Walston,Pui–Yan Kwok,Elad Ziv,Caroline M. Nievergelt,Steven R. Cummings,Anne B. Newman,Russell P. Tracy,Bruce M. Psaty,Alexander P. Reiner	2007	19
18	Common Genetic Variation in the Prothrombin Gene, Hormone Therapy, and Incident Nonfatal Myocardial Infarction in Postmenopausal Women American Journal of Epidemiology ·Lucia A. Hindorff,Bruce M. Psaty,Christopher S. Carlson,Susan R. Heckbert,Thomas Lumley,Nicholas L. Smith,Rozenn N. Lemaître,Mark J. Rieder,Deborah A. Nickerson,Alexander P. Reiner	2006	6
19	Simple estimates of haplotype relative risks in case‐control data Genetic Epidemiology ·Benjamin French,Thomas Lumley,Stephanie A. Monks,Kenneth Rice,Lucia A. Hindorff,Alexander P. Reiner,Bruce M. Psaty	2006	36
20	Polymorphisms of Coagulation Factor XIII Subunit A and Risk of Nonfatal Hemorrhagic Stroke in Young White Women Editorial Comment Stroke ·Alex P. Reiner,Stephen M. Schwartz,Mark Barton Frank,W.T. Longstreth,Lucia A. Hindorff,Gayle Teramura,F.R. Rosendaal,Lakshmi K. Gaur,Bruce M. Psaty,Sreya Antony,Jacques R. Leclerc	2001	37

About Lucia A. Hindorff

Lucia A. Hindorff is a scholar working on Genetics, Hematology, Endocrinology, Diabetes and Metabolism, Cancer Research and Public Health, Environmental and Occupational Health, having authored 64 papers that have together received 8.5k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (17 papers), Genomics and Rare Diseases (16 papers), Ethics in Clinical Research (12 papers), BRCA gene mutations in cancer (11 papers), Hormonal Regulation and Hypertension (8 papers), Blood Coagulation and Thrombosis Mechanisms (7 papers), Bioinformatics and Genomic Networks (6 papers) and Cancer Genomics and Diagnostics (5 papers). The work is most often cited by research in Genetics (4.2k citations), Cancer Research (1.0k citations), Molecular Biology (4.2k citations), Aging (57 citations) and Endocrinology, Diabetes and Metabolism (531 citations). Lucia A. Hindorff has collaborated with scholars based in United States, United Kingdom and Netherlands. Frequent co-authors include Heather Junkins, Teri A. Manolio, Erin M. Ramos, Praveen Sethupathy, Francis S. Collins, Jacqueline A. L. MacArthur, Helen Parkinson, Peggy Hall, Joannella Morales and Paul Flicek. Their work appears in journals such as Genetics in Medicine, European Journal of Human Genetics, American Journal of Hypertension, Clinical and Translational Science and Circulation Cardiovascular Genetics.

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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