James S. Sutcliffe

49.3k citations

92 papers · 9.5k indexed · 3 hit papers · h-index 45

Genetics top 0.05%
- Genetics and Neurodevelopmental Disorders 44
- Genomic variations and chromosomal abnormalities 24
- Genetic Syndromes and Imprinting 17
- Genomics and Rare Diseases 8
Cognitive Neuroscience top 0.5%
- Autism Spectrum Disorder Research 50
Cellular and Molecular Neuroscience top 1%
Molecular Biology top 1%
- Epigenetics and DNA Methylation 12
Developmental Neuroscience top 2%
Epidemiology
- Virology and Viral Diseases 9
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 8

Co-authors: David L. Nelson Arthur L. Beaudet Stephen T. Warren Maura Pieretti Ben A. Oostra Derek P.A. Kuhl C. Thomas Caskey Raymond G. Fenwick
Cited by: Genetics Cognitive Neuroscience Cellular and Molecular Neuroscience
Partner nations: United States Canada Denmark

In The Last Decade

James S. Sutcliffe

90 papers receiving 9.2k 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.

1997 De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome
1992 DNA methylation represses FMR-1 transcription in fragile X syndrome
1991 Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

Peers

Countries citing papers authored by James S. Sutcliffe

Since Specialization

Citations

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

Fields of papers citing papers by James S. Sutcliffe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James S. Sutcliffe. 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 James S. Sutcliffe. The network helps show where James S. Sutcliffe may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Long COVID-19 and Peripheral Serotonin: A Commentary and Reconsideration George P. Anderson,Edwin H. Cook,Randy Blakely,James S. Sutcliffe,Jeremy Veenstra‐VanderWeele	2024	6
2	Characterizing sleep disorders in an autism-specific collection of electronic health records E.V. Singer,Maria Niarchou,Angela Maxwell-Horn,Donald Hucks,Rebecca L. Johnston,James S. Sutcliffe,LK Davis,Beth A. Malow	2022	12
3	Psychometric validation and refinement of the Interoception Sensory Questionnaire (ISQ) in adolescents and adults on the autism spectrum Evan Suzman,Zachary J. Williams,Jacob I. Feldman,Michelle D. Failla,Carissa J. Cascio,Mark T. Wallace,Maria Niarchou,James S. Sutcliffe,Ericka L. Wodka,Tiffany G. Woynaroski	2021	10
4	A Bayesian framework that integrates multi-omics data and gene networks predicts risk genes from schizophrenia GWAS data Quan Wang,Rui Chen,Feixiong Cheng,Qiang Wei,Ying Ji,Yang Hai,Xue Zhong,Ran Tao,Zhexing Wen,James S. Sutcliffe,Chunyu Liu,Edwin H. Cook,Nancy J. Cox,Bingshan Li	2019	84
5	The Gain-of-Function Integrin β3 Pro33 Variant Alters the Serotonin System in the Mouse Brain Michael R. Dohn,Christopher G. Kooker,Lisa Bastarache,Tammy Jessen,Capria Rinaldi,Seth Varney,Matthew D. Mazalouskas,Hope Pan,Kendra H. Oliver,Digna R. Velez Edwards,James S. Sutcliffe,Joshua C. Denny,Ana M.D. Carneiro	2017	21
6	Rare Autism-Associated Variants Implicate Syntaxin 1 (STX1 R26Q) Phosphorylation and the Dopamine Transporter (hDAT R51W) in Dopamine Neurotransmission and Behaviors Etienne Cartier,Peter J. Hamilton,Andrea N. Belovich,Aparna Shekar,Nicholas G. Campbell,Christine Saunders,Thorvald F. Andreassen,Ulrik Gether,Jeremy Veenstra‐VanderWeele,James S. Sutcliffe,Paula G. Ulery-Reynolds,Kevin Erreger,H Matthies,Aurelio Galli	2015	54
7	Integrin β3 Haploinsufficiency Modulates Serotonin Transport and Antidepressant-Sensitive Behavior in Mice Matthew D. Mazalouskas,Tammy Jessen,Seth Varney,James S. Sutcliffe,Jeremy Veenstra‐VanderWeele,Edwin H. Cook,Ana M.D. Carneiro	2015	24
8	Rare coding variants of the adenosine A3 receptor are increased in autism: on the trail of the serotonin transporter regulome Nicholas G. Campbell,Chong-Bin Zhu,Kathryn M. Lindler,Brian L. Yaspan,Emily Kistner‐Griffin,William A. Hewlett,Christopher G. Tate,Randy Blakely,James S. Sutcliffe	2013	18
9	Autism gene variant causes hyperserotonemia, serotonin receptor hypersensitivity, social impairment and repetitive behavior Jeremy Veenstra‐VanderWeele,Christopher L. Muller,Hideki Iwamoto,Jennifer Sauer,William A. Owens,Charisma R. Shah,Jordan Cohen,Padmanabhan Mannangatti,Tammy Jessen,B. J. Thompson,Ran Ye,Travis M. Kerr,Ana M.D. Carneiro,Jacqueline N. Crawley,Elaine Sanders‐Bush,Douglas G. McMahon,Sammanda Ramamoorthy,Lynette C. Daws,James S. Sutcliffe,Randy Blakely	2012	246
10	Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci Lea K. Davis,Eric R. Gamazon,Emily Kistner‐Griffin,Judith A. Badner,Chunyu Liu,Edwin H. Cook,James S. Sutcliffe,Nancy J. Cox	2012	26
11	Colocalization and Regulated Physical Association of Presynaptic Serotonin Transporters with A3 Adenosine Receptors Chong-Bin Zhu,Kathryn M. Lindler,Nicholas G. Campbell,James S. Sutcliffe,William A. Hewlett,Randy Blakely	2011	28
12	Genetic analysis of biological pathway data through genomic randomization Brian L. Yaspan,William S. Bush,Eric S. Torstenson,Deqiong Ma,Margaret A. Pericak‐Vance,Marylyn D. Ritchie,James S. Sutcliffe,Jonathan L. Haines	2011	37
13	Association of MET with social and communication phenotypes in individuals with autism spectrum disorder Jerry L. Campbell,Dana E. Warren,James S. Sutcliffe,Evon Batey Lee,Pat Levitt	2009	39
14	A genetic variant that disrupts MET transcription is associated with autism Jerry L. Campbell,James S. Sutcliffe,Philip J. Ebert,Roberto Militerni,Carmela Bravaccio,Simona Trillo,Maurizio Elia,Cindy Schneider,Raun D. Melmed,Roberto Sacco,Antonio M. Persico,Pat Levitt	2006	310
15	Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility Lauren A. Weiss,Gülüm Kosova,Ryan Delahanty,Lan Jiang,Edwin H. Cook,Carole Ober,James S. Sutcliffe	2006	70
16	Lack of Association Between Autism and SLC25A12 Raquel Rabionet,Jacob L. McCauley,James Jaworski,Allison E. Ashley‐Koch,Eden R. Martin,James S. Sutcliffe,Jonathan L. Haines,G. Robert DeLong,Ruth K. Abramson,Harry H. Wright,Michael L. Cuccaro,John R. Gilbert,Margaret A. Pericak‐Vance	2006	32
17	Autism and 15q11‐q13 disorders: Behavioral, genetic, and pathophysiological issues Elisabeth M. Dykens,James S. Sutcliffe,Pat Levitt	2004	74
18	Identification of a novel paternally expressed transcript adjacent to snRPN in the Prader-Willi syndrome critical region. Yi Ning,Anna V. Roschke,Susan L. Christian,J Lesser,James S. Sutcliffe,David H. Ledbetter	1996	22
19	Imprinting analysis of three genes in the Prader — Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E) Mltsuyoshl Nakao,James S. Sutcliffe,Becky Durtschl,Aplwat Mutlrangura,David H. Ledbetter,Arthur L. Beaudet	1994	96
20	DNA methylation represses FMR-1 transcription in fragile X syndromebreakdown → James S. Sutcliffe,David L. Nelson,Fuping Zhang,Maura Pieretti,C. Thomas Caskey,Debra Saxe,Stephen T. Warren	1992	557

About James S. Sutcliffe

James S. Sutcliffe is a scholar working on Cognitive Neuroscience, Genetics and Psychiatry and Mental health, having authored 92 papers that have together received 9.5k indexed citations. Recurring topics across this work include Autism Spectrum Disorder Research (50 papers), Genetics and Neurodevelopmental Disorders (44 papers), Genomic variations and chromosomal abnormalities (24 papers), Genetic Syndromes and Imprinting (17 papers), Epigenetics and DNA Methylation (12 papers), Virology and Viral Diseases (9 papers), Genomics and Rare Diseases (8 papers) and Prenatal Screening and Diagnostics (8 papers). The work is most often cited by research in Genetics (6.7k citations), Cognitive Neuroscience (3.9k citations) and Cellular and Molecular Neuroscience (1.4k citations). James S. Sutcliffe has collaborated with scholars based in United States, Canada and Denmark. Frequent co-authors include David L. Nelson, Arthur L. Beaudet, Stephen T. Warren, Maura Pieretti, Ben A. Oostra, Derek P.A. Kuhl, C. Thomas Caskey, Raymond G. Fenwick, Stephen Richards and Ying‐Hui Fu.

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