Audrey E. Hendricks

9.5k citations

77 papers · 4.0k · 1 hit paper · h-index 28

Impact in

Genetics top 2%
- Genetic Associations and Epidemiology
- Genomics and Rare Diseases
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
Endocrine and Autonomic Systems top 2%
- Regulation of Appetite and Obesity

Papers in

Genetics 28
- Genetic Associations and Epidemiology 23
- Genomics and Rare Diseases 8
- Genetic Mapping and Diversity in Plants and Animals 7
- Genetic and phenotypic traits in livestock 5
Neurology 10
- Neurological disorders and treatments 6
- Parkinson's Disease Mechanisms and Treatments 5

Co-authors: Vanessa C. Wheeler (3 shared papers)Tammy Gillis (3 shared papers)Richard H. Myers (5 shared papers)Jayalakshmi Srinidhi Mysore (2 shared papers)Meera Swami (1 shared paper)Nancy F. Krebs (20 shared papers)Minghua Tang (15 shared papers)Marcy E. MacDonald (3 shared papers)
Journals: Nature Communications (8 papers)The American Journal of Human Genetics (5 papers)Current Developments in Nutrition (5 papers)Scientific Reports (3 papers)Nutrients (2 papers)
Partner nations: United States United Kingdom China

In The Last Decade

Audrey E. Hendricks

71 papers receiving 3.9k citations

Audrey E. Hendricks's Hit Papers

align trajectories log scale

The UK10K project identifies rare variants in health and disease 2015 · 760 citations

What are hit papers?

Paper score: A paper's citations measured against the top-1% bar of its own field and year: the square root of citations ÷ bar, so 1 means right at the bar and 2 means four times its citations. The bar blends the citation counts that enter the top 1% of the paper's subfields in its year (weighted 89.5%), of those subfields over all years (0.5%) and of its year across all fields (10%); a subfield and year with fewer than 400 papers takes its year's bar. Papers from 2026 are not scored yet: in an unfinished year, when a paper appeared matters more than how it is cited.

Hit paper: A paper cited at least 1.5× the top-1% bar of its field and year: a paper score of at least √1.5.

2015 Nature

Peers

Countries citing papers authored by Audrey E. Hendricks

Since Specialization

Citations

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

Fields of papers citing papers by Audrey E. Hendricks

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Audrey E. Hendricks. 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 Audrey E. Hendricks. The network helps show where Audrey E. Hendricks may publish in the future.

Co-authors

The 25 scholars most cited alongside Audrey E. Hendricks, 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 Audrey E. Hendricks Line = papers co-authored together Audrey E. Hendricks links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 77 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	The UK10K project identifies rare variants in health and disease Nature ·Josine L. Min, Jie Huang, Yasin Memari, Shane McCarthy, Changjiang Xu, Marta Futema, Valentina Iotchkova, Stephan Schiffels Hit paper breakdown →	2015	760
2	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity Nature Genetics ·Valérie Turcot, Yingchang Lu, Heather M. Highland, Claudia Schurmann, Anne E. Justice, Rebecca S. Fine, Jonathan P. Bradfield, Tõnu Esko	2017	307
3	The UK10K project identifies rare variants in health and disease Kölner Universitäts PublikationsServer (Universität zu Köln) ·Klaudia Walter, Josine L. Min, Jie Huang, Lucy Crooks, Yasin Memari, Shane McCarthy, John Richard Perry, Changjiang Xu	2015	285
4	Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset Human Molecular Genetics ·Meera Swami, Audrey E. Hendricks, Tammy Gillis, Tiffany Massood, Jayalakshmi Srinidhi Mysore, Richard H. Myers, Vanessa C. Wheeler	2009	255
5	Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel Nature Communications ·Jie Huang, Bryan Howie, Shane McCarthy, Yasin Memari, Klaudia Walter, Josine L. Min, Petr Danecek, Giovanni Malerba	2015	253
6	Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes Neurobiology of Disease ·Ella Dragileva, Audrey E. Hendricks, Allison Teed, Tammy Gillis, Edith Lopez, Errol C. Friedberg, Raju Kucherlapati, Winfried Edelmann	2008	186
7	KSR2 Mutations Are Associated with Obesity, Insulin Resistance, and Impaired Cellular Fuel Oxidation Cell ·Laura R. Pearce, Neli Atanassova, Matthew C. Banton, Bill Bottomley, Agatha A. van der Klaauw, Jean‐Pierre Revelli, Audrey E. Hendricks, Julia M. Keogh	2013	155
8	Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits The American Journal of Human Genetics ·Ioanna Tachmazidou, Dániel Süveges, Josine L. Min, Graham R. S. Ritchie, Julia Steinberg, Klaudia Walter, Valentina Iotchkova, Jeremy Schwartzentruber	2017	132
9	Body mass index is negatively associated with telomere length: a collaborative cross-sectional meta-analysis of 87 observational studies American Journal of Clinical Nutrition ·Marij Gielen, Geja J. Hageman, Evangelia E. Antoniou, Katarina Nordfjäll, Massimo Mangino, Muthuswamy Balasubramanyam, Tim De Meyer, Audrey E. Hendricks	2018	131
10	Genetic architecture of human thinness compared to severe obesity PLoS Genetics ·Fernando Riveros Mckay Aguilera, Vanisha Mistry, Rebecca Bounds, Audrey E. Hendricks, Julia M. Keogh, H. Thomas, Elana Henning, Laura J. Corbin	2019	104
11	Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance Cell ·Agatha A. van der Klaauw, Sophie Croizier, Edson Mendes de Oliveira, Lukas Kurt Josef Stadler, Soyoung Park, Youxin Kong, Matthew C. Banton, Panna Tandon	2019	104
12	Haplotypes and gene expression implicate the MAPT region for Parkinson disease Neurology ·Jennifer E. Tobin, Jeanne C. Latourelle, Mark Lew, Christine Klein, Oksana Suchowersky, Holly A. Shill, Lawrence I. Golbe, M. H. Mark	2008	93
13	The Gly2019Ser mutation in LRRK2is not fully penetrant in familial Parkinson's disease: the GenePD study BMC Medicine ·Jeanne C. Latourelle, Mei Sun, Mark Lew, Oksana Suchowersky, Christine Klein, Lawrence I. Golbe, Margery H. Mark, John H. Growdon	2008	89
14	Whole-genome sequence-based analysis of thyroid function Nature Communications ·Peter Nicholas Taylor, Eleonora Porcu, Shelby Chew, Purdey J. Campbell, Michela Traglia, Suzanne J. Brown, Benjamin H. Mullin, Hashem A. Shihab	2015	87
15	Iron in Micronutrient Powder Promotes an Unfavorable Gut Microbiota in Kenyan Infants Nutrients ·Minghua Tang, Daniel N. Frank, Audrey E. Hendricks, Diana Ir, Fabian Esamai, Edward A. Liechty, K. Michael Hambidge, Nancy F. Krebs	2017	80
16	Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis Nature Communications ·Agatha A. van der Klaauw, Liangru Zhu, Tessa Cacciottolo, Yanlin He, Lukas Kurt Josef Stadler, Chunmei Wang, Pingwen Xu, Kenji Saito	2019	63
17	Exome Sequencing Identifies Genes and Gene Sets Contributing to Severe Childhood Obesity, Linking PHIP Variants to Repressed POMC Transcription Cell Metabolism ·Gaëlle Marenne, Audrey E. Hendricks, Aliki Perdikari, Rebecca Bounds, Felicity Payne, Julia M. Keogh, Christopher J. Lelliott, Elana Henning	2020	60
18	A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans Nature Communications ·Nicholas John Timpson, Klaudia Walter, Josine L. Min, Ioanna Tachmazidou, Giovanni Malerba, So–Youn Shin, Lu Chen, Marta Futema	2014	58
19	Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity Scientific Reports ·Audrey E. Hendricks, Elena G. Bochukova, Gaëlle Marenne, Julia M. Keogh, Neli Atanassova, Rebecca Bounds, Eleanor Wheeler, Vanisha Mistry	2017	58
20	TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport Nature Communications ·Miriam Schmidts, Yuqing Hou, Claudio R. Cortés, Dorus A. Mans, Céline Huber, Karsten Boldt, Mitali Patel, Jeroen van Reeuwijk	2015	51

About Audrey E. Hendricks

Audrey E. Hendricks is a scholar working on Genetics, Neurology, Cellular and Molecular Neuroscience, Physiology and Nutrition and Dietetics, having authored 77 papers that have together received 4.0k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (23 papers), Genomics and Rare Diseases (8 papers), Genetic Mapping and Diversity in Plants and Animals (7 papers), Neurological disorders and treatments (6 papers), Genetic Neurodegenerative Diseases (6 papers), Genetic and phenotypic traits in livestock (5 papers), Parkinson's Disease Mechanisms and Treatments (5 papers) and Metabolomics and Mass Spectrometry Studies (5 papers). The work is most often cited by research in Genetics (1.5k citations), Endocrine and Autonomic Systems (297 citations), Cellular and Molecular Neuroscience (597 citations), Molecular Biology (1.6k citations) and Neurology (327 citations). Audrey E. Hendricks has collaborated with scholars based in United States, United Kingdom and China. Frequent co-authors include Vanessa C. Wheeler, Tammy Gillis, Richard H. Myers, Jayalakshmi Srinidhi Mysore, Meera Swami, Nancy F. Krebs, Minghua Tang, Marcy E. MacDonald, Kathryn L. Lunetta and Errol C. Friedberg. Their work appears in journals such as Nature Communications, The American Journal of Human Genetics, Current Developments in Nutrition, Scientific Reports and Nutrients.

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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Audrey E. Hendricks

Audrey E. Hendricks's Hit Papers

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About Audrey E. Hendricks

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