Robin Sherrington

13.7k citations

47 papers · 3.2k indexed · h-index 25

Impact in

Genetics top 1%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Biological Psychiatry top 5%

Papers in

Genetics 24
- Genetic Associations and Epidemiology 16
- Genomic variations and chromosomal abnormalities 12
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 4
Psychiatry and Mental health 8
- Bipolar Disorder and Treatment 5

Co-authors: Hannes Pétursson Jon Brynjolfsson David Curtis Peter St George‐Hyslop Sarah H. Shaw Hugh Gurling H. Gurling Mark D. Potter
Journals: Genomics (4 papers)Nature (3 papers)The American Journal of Human Genetics (3 papers)American Journal of Psychiatry (3 papers)Psychiatric Genetics (3 papers)
Partner nations: United Kingdom United States Iceland

In The Last Decade

Robin Sherrington

47 papers receiving 3.1k citations

Peers

Countries citing papers authored by Robin Sherrington

Since Specialization

Citations

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

Fields of papers citing papers by Robin Sherrington

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robin Sherrington. 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 Robin Sherrington. The network helps show where Robin Sherrington may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	Stereoselective Analysis of the Antiseizure Activity of Fenfluramine and Norfenfluramine in Mice: Is l-Norfenfluramine a Better Follow-Up Compound to Racemic-Fenfluramine? International Journal of Molecular Sciences ·Natalia Erenburg, Emilio Perucca, Jeff Bechard, Céline Dubé, Nina Weishaupt, Robin Sherrington, Meir Bialer	2024	4
2	Identification of four novel genes contributing to familial elevated plasma HDL cholesterol in humans Journal of Lipid Research ·Roshni R. Singaraja, Ian Tietjen, G. Kees Hovingh, Patrick L. Franchini, Chris Radomski, Kenny K. Wong, Margaret vanHeek, Ioannis M. Stylianou, Linus Lin, Liangsu Wang, Lyndon J. Mitnaul, Brian K. Hubbard, Michael D. Winther, Maryanne Mattice, Annick Legendre, Robin Sherrington, John J.P. Kastelein, Karen Akinsanya, Andrew Plump, Michael R. Hayden	2014	15
3	Treatment of Nav1.7-mediated pain in inherited erythromelalgia using a novel sodium channel blocker Pain ·Yigal Paul Goldberg, Nicola Price, Rostam Namdari, Charles J. Cohen, Mieke H Lamers, Conrad Winters, James J. Price, Clint E. Young, Henry Verschoof, Robin Sherrington, Simon N. Pimstone, Michael R. Hayden	2011	108
4	A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12 Molecular Psychiatry ·Éric Shink, J Morissette, Robin Sherrington, Nicholas Barden	2004	59
5	Genome‐wide scan for linkage to schizophrenia in a Spanish‐origin cohort from Costa Rica American Journal of Medical Genetics ·Lynn E. DeLisi, Andrea Mesén, Carlos Rodriguez, Arturo Bertheau, Beatrice LaPrade, Michelle Llach, Silvina Riondet, Kamran Razi, Margaret Relja, William Byerley, Robin Sherrington	2002	70
6	A Schizophrenia-Susceptibility Locus at 6q25, in One of the World's Largest Reported Pedigrees The American Journal of Human Genetics ·Eva Lindholm, Birgit Ekholm, Sarah H. Shaw, Paula Jalonen, Gunnel Johansson, Ulf Pettersson, Robin Sherrington, Rolf Adolfsson, Elena Jazin	2001	111
7	Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder American Journal of Medical Genetics ·Lynn E. DeLisi, Sarah H. Shaw, Robin Sherrington, Betsy Nanthakumar, G. Shields, Angela Smith, Nigel Wellman, Veronica W. Larach, J. Loftus, Kamran Razi, Jason A. Stewart, Margherita Comazzi, Antonio Vita, Marc D. Binder, Timothy J. Crow	2000	29
8	New DNA markers with increased informativeness show diminished support for a chromosome 5q11–13 schizophrenia susceptibility locus and exclude linkage in two new cohorts of British and Icelandic families Annals of Human Genetics ·Gursharan Kalsi, Baljinder S. Mankoo, David Curtis, Robin Sherrington, Georg Melmer, Jon Brynjolfsson, T. Sigmundsson, Timothy D. Read, P. Murphy, Hannes Pétursson, H. Gurling	1999	11
9	A genome-wide search for schizophrenia susceptibility genes American Journal of Medical Genetics ·Sarah H. Shaw, Mary T. Kelly, Angela Smith, Gail Shields, Penelope J. Hopkins, J. Loftus, Steven H. Laval, Antonio Vita, Marc D. Binder, Lon R. Cardon, Timothy J. Crow, Robin Sherrington, Lynn E. DeLisi	1998	208
10	Presenilin Proteins Undergo Heterogeneous Endoproteolysis between Thr291and Ala299and Occur as Stable N- and C-Terminal Fragments in Normal and Alzheimer Brain Tissue Neurobiology of Disease ·Marcia B. Podlisny, Martin Citron, Patricia Amarante, Robin Sherrington, Weiming Xia, Jimin Zhang, Thekla S. Diehl, George Levesque, Paul Fraser, Christian Haass, Edward H. Koo, Peter Seubert, Peter St George‐Hyslop, David B. Teplow, Dennis J. Selkoe	1997	250
11	Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant Human Molecular Genetics ·Robin Sherrington	1996	215
12	Linkage analysis of chromosome 22q12–13 in a United Kingdom/Icelandic sample of 23 multiplex schizophrenia families American Journal of Medical Genetics ·Gursharan Kalsi, Jon Brynjolfsson, Robert J. Butler, Robin Sherrington, David Curtis, Thordur Sigmundsson, Timothy Read, P. Murphy, T. Sharma, Hannes Pétursson, Hmd Gurling	1995	32
13	Segregation and linkage analysis in five manic depression pedigrees excludes the 5HT1a receptor gene (HTR1A) Annals of Human Genetics ·David Curtis, Jon Brynjolfsson, Hannes Pétursson, Susan Holmes, Robin Sherrington, Peter Brett, Larry Rifkin, P. Murphy, E. Moloney, Georg Melmer, Hugh Gurling	1993	15
14	Cloning of the Human Dopamine D5 Receptor Gene and Identification of a Highly Polymorphic Microsatellite for the DRD5 Locus That Shows Tight Linkage to the Chromosome 4p Reference Marker RAF1P1 Genomics ·Robin Sherrington, Baljinder S. Mankoo, (unknown), Gursharon Kalsi, David Curtis, Kenneth H. Buetow, Sue Povey, Hugh Gurling	1993	54
15	Linkage analysis in a large pedigree multiply affected with Gilles de la Tourette syndrome UCL Discovery (University College London) ·PM Brett, David Curtis, Georg Melmer, Robin Sherrington, Deborah Holmes, Michael Robertson, H. Gurling	1991	1
16	Two microsatellite polymorphisms at the D5S39 locus Nucleic Acids Research ·Baljinder S. Mankoo, Robin Sherrington, Amador De La Concha, Gursharan Kalsi, David Curtis, Georg Melmer, Hugh Gurling	1991	25
17	Exclusion of linkage to 5qll–13 in families with schizophrenia and other psychiatric disorders Nature ·Sevilla D. Detera‐Wadleigh, Lynn R. Goldin, Robin Sherrington, Ignacio Encı́o, Carlos de Miguel, Wade H. Berrettini, Hugh Gurling, Elliot S. Gershon	1989	78
18	Recent and Future Molecular Genetic Research Into Schizophrenia Schizophrenia Bulletin ·Hugh Gurling, Robin Sherrington, Jon Brynjolfsson, Timothy Read, David Curtis, B. J. Mankoo, Mark D. Potter, Hannes Pétursson	1989	6
19	Molecular genetics and heterogeneity in manic depression Molecular Neurobiology ·Hugh Gurling, Robin Sherrington, Jon Brynjolfsson, Mark D. Potter, Melvin G. McInnis, Hannes Pétursson, S. Hodgkinson	1988	5
20	Localization of a susceptibility locus for schizophrenia on chromosome 5 Nature ·Robin Sherrington, Jon Brynjolfsson, Hannes Pétursson, Mark D. Potter, Keith E. Dudleston, B. M. Barraclough, John J. Wasmuth, Mark Dobbs, H. Gurling	1988	402

About Robin Sherrington

Robin Sherrington is a scholar working on Genetics, Psychiatry and Mental health, Physiology, Pharmacology and Molecular Biology, having authored 47 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (16 papers), Genomic variations and chromosomal abnormalities (12 papers), Alzheimer's disease research and treatments (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), Bipolar Disorder and Treatment (5 papers), Autism Spectrum Disorder Research (5 papers), Genomics and Rare Diseases (4 papers) and Receptor Mechanisms and Signaling (3 papers). The work is most often cited by research in Genetics (1.4k citations), Biological Psychiatry (116 citations), Physiology (999 citations), Psychiatry and Mental health (533 citations) and Cellular and Molecular Neuroscience (502 citations). Robin Sherrington has collaborated with scholars based in United Kingdom, United States and Iceland. Frequent co-authors include Hannes Pétursson, Jon Brynjolfsson, David Curtis, Peter St George‐Hyslop, Sarah H. Shaw, Hugh Gurling, H. Gurling, Mark D. Potter, B. M. Barraclough and John J. Wasmuth. Their work appears in journals such as Genomics, Nature, The American Journal of Human Genetics, American Journal of Psychiatry and Psychiatric 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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