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Jerry L. Campbell

ResearcherPublications, citations & collaboration network

Jerry L. Campbell is a researcher indexed in ScholarIQ from OpenAlex & ORCID. ScholarIQ records 166 works, 9,995 citations, an h-index of 43 and an i10-index of 103.

166
Works
9,995
Citations
43
h-index
103
i10-index

How has Jerry L. Campbell's publication output changed over time?

ScholarIQpublication output · 1998–2013

Output grew0% over the shown period — from 1 works in 1998 to 1 in 2013.

1
1
1
1
2
1
1
1
1
1
1998200320062007200820092010201120122013

What are the most-cited papers on Jerry L. Campbell?

ScholarIQmost cited works
Copper, iron and zinc in Alzheimer's disease senile plaques
Mark A. Lovell, J. David Robertson, W.J. Teesdale, Jerry L. Campbell, William R. Markesbery
Journal of the Neurological Sciences. 19982,112 Citations
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
Brett S. Abrahams, Dan E. Arking, Jerry L. Campbell, Heather C. Mefford, Eric M. Morrow, Lauren A. Weiss, Idan Menashe, Tim Wadkins, Sharmila Banerjee‐Basu, Alan Packer
Molecular Autism. 2013955 CitationsOPEN ACCESS
Evaluation, Diagnosis, and Treatment of Gastrointestinal Disorders in Individuals With ASDs: A Consensus Report
Timothy Buie, Jerry L. Campbell, George J. Fuchs, Glenn T. Furuta, Joseph Levy, Judy VandeWater, Agnes H. Whitaker, Dan Atkins, Margaret L. Bauman, Arthur L. Beaudet, Edward G. Carr, Michael D. Gershon, Susan Hyman, Pipop Jirapinyo, Harumi Jyonouchi, Koorosh Kooros, Rafail I. Kushak, Pat Levitt, Susan E. Levy, Jeffery D. Lewis, Katherine F. Murray, Marvin R. Natowicz, Aderbal Sabrá, Barry K. Wershil, Sharon Weston, Lonnie K. Zeltzer, Harland S. Winter
PEDIATRICS. 2010874 Citations
A genetic variant that disrupts <i>MET</i> 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
Proceedings of the National Academy of Sciences. 2006407 CitationsOPEN ACCESS
Genetic Disruption of Cortical Interneuron Development Causes Region- and GABA Cell Type-Specific Deficits, Epilepsy, and Behavioral Dysfunction
Elizabeth M. Powell, Jerry L. Campbell, Gregg D. Stanwood, Caleb Davis, Jeffrey L. Noebels, Pat Levitt
Journal of Neuroscience. 2003337 CitationsOPEN ACCESS

Related on ScholarIQ

Grand Rapids Community College
Institution
Copper, iron and zinc in Alzheimer's disease senile plaques
Paper
SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)
Paper
Evaluation, Diagnosis, and Treatment of Gastrointestinal Disorders in Individuals With ASDs: A Consensus Report
Paper
A genetic variant that disrupts <i>MET</i> transcription is associated with autism
Paper
Genetic Disruption of Cortical Interneuron Development Causes Region- and GABA Cell Type-Specific Deficits, Epilepsy, and Behavioral Dysfunction
Paper
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