David J. Cutler

25.3k citations

125 papers · 6.1k indexed · 1 hit paper · h-index 39

Impact in

Endocrine and Autonomic Systems top 0.5%
- Circadian rhythm and melatonin
Genetics top 0.5%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genetic Mapping and Diversity in Plants and Animals
- Genomic variations and chromosomal abnormalities

Papers in

Genetics 54
- Genetic Associations and Epidemiology 16
- Genomic variations and chromosomal abnormalities 15
- Genetics and Neurodevelopmental Disorders 12
- Genetic Mapping and Diversity in Plants and Animals 11
- Genomics and Rare Diseases 10
Endocrine and Autonomic Systems 13
- Circadian rhythm and melatonin 10

Co-authors: Gonçalo R. Abecasis Janis Wigginton Shin Lin Aravinda Chakravarti Michael E. Zwick Hugh D. Piggins Gareth Williams Richard O. Day
Journals: The American Journal of Human Genetics (10 papers)Genetics (5 papers)European Journal of Pharmacology (3 papers)Journal of Raman Spectroscopy (3 papers)G3 Genes Genomes Genetics (3 papers)
Partner nations: United States United Kingdom Australia

In The Last Decade

David J. Cutler

120 papers receiving 6.0k citations

Hit Papers

align trajectories log scale

A Note on Exact Tests of Hardy-Weinberg Equilibrium 2005 · 1.1k citations

Peers

Countries citing papers authored by David J. Cutler

Since Specialization

Citations

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

Fields of papers citing papers by David J. Cutler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David J. Cutler. 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 David J. Cutler. The network helps show where David J. Cutler may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Sex differences in brain protein expression and disease Nature Medicine ·Aliza P. Wingo, Yue Liu, Ekaterina S. Gerasimov, Selina Vattathil, Jiaqi Liu, David J. Cutler, Michael P. Epstein, Gabriëlla A.M. Blokland, Madhav Thambisetty, Juan C. Troncoso, Duc M. Duong, David A. Bennett, Allan I. Levey, Nicholas T. Seyfried, Thomas S. Wingo	2023	37
2	Evaluation of AQP4 functional variants and its association with fragile X-associated tremor/ataxia syndrome Frontiers in Aging Neuroscience ·Andrea Elias-Mas, Míriam Potrony, Jaume Bagué, David J. Cutler, María Isabel Álvarez‐Mora, Teresa Torres, Tamara Barcos, Joan Anton Puig‐Butillé, Marta Rubio, Irene Madrigal, Susana Puig, Emily G. Allen, Laia Rodríguez‐Revenga	2023	3
3	Characterization of Intestinal Mesenchymal Stromal Cells From Patients With Inflammatory Bowel Disease for Autologous Cell Therapy Stem Cells Translational Medicine ·Murugadas Anbazhagan, Duke Geem, Suresh Venkateswaran, Ranjit Pelia, Vasantha L. Kolachala, Anne Dodd, Sushma Chowdary Maddipatla, David J. Cutler, Jason D. Matthews, Raghavan Chinnadurai, Subra Kugathasan	2023	7
4	Methylation quantitative trait loci are largely consistent across disease states in Crohn’s disease G3 Genes Genomes Genetics ·Suresh Venkateswaran, Hari K. Somineni, Varun Kilaru, Şeyma Katrinli, Jarod Prince, David T. Okou, Jeffrey S. Hyams, Lee A. Denson, Richárd Kellermayer, Greg Gibson, David J. Cutler, Alicia K. Smith, Subra Kugathasan, Karen N. Conneely	2022	4
5	Leveraging Family History in Case-Control Analyses of Rare Variation Genetics ·Claudia Solís‐Lemus, Sebastian Fischer, Andrei Todor, Cuining Liu, Elizabeth J. Leslie, David J. Cutler, Debashis Ghosh, Michael P. Epstein	2019	0
6	Restoration of pyrethroid susceptibility in a highly resistant Aedes aegypti population Biology Letters ·Marissa K. Grossman, Valentín Uc-Puc, Julián Rodrı́guez, David J. Cutler, Levi T. Morran, Pablo Manrique‐Saide, Gonzalo M. Vazquez‐Prokopec	2018	28
7	Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects G3 Genes Genomes Genetics ·Benjamin L. Rambo‐Martin, Jennifer G. Mulle, David J. Cutler, Lora Jh Bean, Tracie C. Rosser, Kenneth J. Dooley, L. Clifford, George Capone, Cheryl L. Maslen, Roger H. Reeves, Stephanie L. Sherman, Michael E. Zwick	2017	11
8	Rigor of non‐dairy galactose restriction in early childhood, measured by retrospective survey, does not associate with severity of five long‐term outcomes quantified in 231 children and adults with classic galactosemia Journal of Inherited Metabolic Disease ·Allison B. Frederick, David J. Cutler, Judith L. Fridovich‐Keil	2017	18
9	MPD: multiplex primer design for next-generation targeted sequencing BMC Bioinformatics ·Thomas S. Wingo, Alex Kotlar, David J. Cutler	2017	20
10	Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples Nature Genetics ·Jack A. Kosmicki, Kaitlin E. Samocha, Daniel P. Howrigan, Stephan Sanders, Kamil Slowikowski, Monkol Lek, Konrad J. Karczewski, David J. Cutler, Bernie Devlin, Kathryn Roeder, Joseph D. Buxbaum, Benjamin M. Neale, Daniel G. MacArthur, Dennis P. Wall, Elise Robinson, Mark J. Daly	2017	183
11	Contribution of copy-number variation to Down syndrome–associated atrioventricular septal defects Genetics in Medicine ·Dhanya Ramachandran, Jennifer G. Mulle, Adam E. Locke, Lora Jh Bean, Tracie C. Rosser, Promita Bose, Kenneth J. Dooley, L. Clifford, George Capone, Roger H. Reeves, Cheryl L. Maslen, David J. Cutler, Stephanie L. Sherman, Michael E. Zwick	2014	20
12	Common NOD2 risk variants in African Americans with Crohnʼs disease are due exclusively to recent Caucasian admixture Inflammatory Bowel Diseases ·Oloruntosin Adeyanju, David T. Okou, Clifton Huang, Archana Kumar, Cary G. Sauer, Courtney Galloway, Mahadev Prasad, Jon Waters, David J. Cutler, Michael E. Zwick, Tanvi Dhere, Subra Kugathasan	2012	16
13	The Heritability of Amyotrophic Lateral Sclerosis in a Clinically Ascertained United States Research Registry PLoS ONE ·Thomas S. Wingo, David J. Cutler, Nicole Yarab, Crystal Kelly, Jonathan D. Glass	2011	49
14	Association study of serotonin pathway genes in attempted suicide American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Jennifer Judy, Fayaz Seifuddin, Pamela B. Mahon, Yuqing Huo, Fernando S. Goes, Dubravka Jancic, Barbara Schweizer, Francis M. Mondimore, Dean F. MacKinnon, J. Raymond DePaulo, Elliot S. Gershon, Francis J. McMahon, David J. Cutler, Peter P. Zandi, James B. Potash, Virginia L. Willour	2011	12
15	Evaluation of safety and pharmacokinetics of a fully human IGF-1 receptor antibody, SCH 717454, in healthy volunteers Molecular Cancer Therapeutics ·Jabed Seraj, Max Tsai, Michael Seiberling, David J. Cutler	2007	8
16	Relative Contribution of Genetic and Nongenetic Modifiers to Intestinal Obstruction in Cystic Fibrosis Gastroenterology ·Scott M. Blackman, Rebecca Deering–Brose, Rita McWilliams, Kathleen Naughton, Barbara Coleman, Teresa Y.Y. Lai, Marilyn Algire, Suzanne E. Beck, Julie Hoover‐Fong, Ada Hamosh, M. Daniele Fallin, Kristen M. West, Dan E. Arking, Aravinda Chakravarti, David J. Cutler, Garry R. Cutting	2006	101
17	On the probability that a novel variant is a disease-causing mutation Genome Research ·Adele A. Mitchell, Aravinda Chakravarti, David J. Cutler	2005	21
18	Orexin-A immunoreactive neurons in the rat hypothalamus do not contain neuronal nitric oxide synthase (nNOS) Peptides ·David J. Cutler, Richard Morris, Martyn L. Evans, Ron A. Leslie, Jonathan R.S. Arch, Gareth Williams	2001	19
19	Estimating Divergence Times in the Presence of an Overdispersed Molecular Clock Molecular Biology and Evolution ·David J. Cutler	2000	81
20	Effects of ionophoretically applied bombesin-like peptides on hamster suprachiasmatic nucleus neurons in vitro European Journal of Pharmacology ·Hugh D. Piggins, David J. Cutler, Benjamin Rusak	1994	24

About David J. Cutler

David J. Cutler is a scholar working on Genetics, Endocrine and Autonomic Systems, Ophthalmology, Cognitive Neuroscience and Biophysics, having authored 125 papers that have together received 6.1k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (16 papers), Genomic variations and chromosomal abnormalities (15 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genetic Mapping and Diversity in Plants and Animals (11 papers), Circadian rhythm and melatonin (10 papers), Sleep and Wakefulness Research (10 papers), Genomics and Rare Diseases (10 papers) and Drug-Induced Ocular Toxicity (9 papers). The work is most often cited by research in Endocrine and Autonomic Systems (829 citations), Genetics (2.3k citations), Cognitive Neuroscience (989 citations), Biological Psychiatry (84 citations) and Behavioral Neuroscience (116 citations). David J. Cutler has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Gonçalo R. Abecasis, Janis Wigginton, Shin Lin, Aravinda Chakravarti, Michael E. Zwick, Hugh D. Piggins, Aravinda Chakravarti, Gareth Williams, Richard O. Day and Joanne A. Harrold. Their work appears in journals such as The American Journal of Human Genetics, Genetics, European Journal of Pharmacology, Journal of Raman Spectroscopy and G3 Genes Genomes 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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