John B. Vincent

21.8k citations

126 papers · 4.4k indexed · h-index 37

Impact in

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

Papers in

Genetics 71
- Genetics and Neurodevelopmental Disorders 54
- Genomic variations and chromosomal abnormalities 23
- Genomics and Rare Diseases 16
- Genetic Associations and Epidemiology 8
Biological Psychiatry 3

Co-authors: Muhammad Ayub Stephen W. Scherer James L. Kennedy Abdul Noor Hugh Gurling Mark A. Ditmer Leland K. Werden George D. Weiblen
Journals: The American Journal of Human Genetics (9 papers)Psychiatric Genetics (6 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (6 papers)Human Molecular Genetics (5 papers)Molecular Psychiatry (4 papers)
Partner nations: Canada United States United Kingdom

In The Last Decade

John B. Vincent

121 papers receiving 4.3k citations

Peers

Countries citing papers authored by John B. Vincent

Since Specialization

Citations

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

Fields of papers citing papers by John B. Vincent

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John B. Vincent. 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 John B. Vincent. The network helps show where John B. Vincent may publish in the future.

Co-authors

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

All Works

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20 of 20 papers shown

#	Work
1	The role of amylin, a gut–brain axis hormone, in metabolic and neurological disorders FASEB BioAdvances ·Tahir Muhammad, Stephen F. Pastore, Katrina Good, Wai Haung Yu, John B. Vincent	2025	2
2	Computational screening of antiviral candidates for Monkeypox virus DNA polymerase and A42R protein PLoS neglected tropical diseases ·Muhammad Waqas Amjid, Muhammad Maroof Khan, Stephen F. Pastore, John B. Vincent, Tahir Muhammad	2025	0
3	Biallelic variants identified in 36 Pakistani families and trios with autism spectrum disorder Scientific Reports ·Hamid Khan, Ricardo Harripaul, Anna Mikhailov, Sumayah Herzi, Sonya Bowers, Muhammad Ayub, Muhammad Imran Shabbir, John B. Vincent	2024	1
4	Interplay between polygenic risk for mood disorders and stressful life events in bipolar disorder Journal of Affective Disorders ·Georgina M. Hosang, Sania Shakoor, Nicole King, Marcos Sanches, John B. Vincent, James L. Kennedy, Peter McGuffin, Robert Keers, Clement C. Zai	2024	1
5	The Development of Mental Health Difficulties in Young People With and Without Developmental Language Disorder: A Gene–Environment Interplay Study Using Polygenic Scores Journal of Speech Language and Hearing Research ·Umar Toseeb, John B. Vincent, Olakunle Oginni, Kathryn Asbury, Dianne F. Newbury	2023	9
6	Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations Translational Psychiatry ·Rebecca S.F. Mok, Wenbo Zhang, Taimoor I. Sheikh, Kartik S. Pradeepan, Isabella Rodrigues Fernandes, Leah C. DeJong, Gabriel Benigno, Matthew R. Hildebrandt, Marat Mufteev, Deivid C. Rodrigues, Wei Wei, Alina Piekna, Jiajie Liu, Alysson R. Muotri, John B. Vincent, Lyle Muller, Julio Martínez-Trujillo, Michael W. Salter, James Ellis	2022	15
7	Genome-wide association study of suicidal behaviour severity in mood disorders The World Journal of Biological Psychiatry ·Clement C. Zai, Chiara Fabbri, Georgina M. Hosang, Ruo Su Zhang, Emiko Koyama, Vincenzo De Luca, Arun K. Tiwari, Nicole King, John S. Strauss, Ian Jones, Lisa Jones, Gerome Breen, Anne Farmer, Peter McGuffin, John B. Vincent, James L. Kennedy, Cathryn M. Lewis	2021	8
8	Differential Allelic Expression of HTR1B in Suicide Victims: Genetic and Epigenetic Effect of the <b><i>Cis</i></b>-Acting Variants Neuropsychobiology ·Ali Bani‐Fatemi, Aaron Howe, Clement C. Zai, James L. Kennedy, John B. Vincent, John S. Strauss, Albert H.C. Wong, Vincenzo De Luca	2016	1
9	Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability Psychiatric Genetics ·Nasim Vasli, Iltaf Ahmed, Kirti Mittal, Mehrnaz Ohadi, Anna Mikhailov, Muhammad Rafiq, Attya Bhatti, Melissa T. Carter, Danielle M. Andrade, Muhammad Ayub, John B. Vincent, Peter John	2015	17
10	A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family Human Molecular Genetics ·Muzammil Ahmad Khan, Verena Rupp, Meritxell Orpinell, Muhammad Sajid Hussain, Janine Altmüller, Michel O. Steinmetz, Christian Enzinger, Hölger Thiele, Wolfgang Höhne, Gudrun Nürnberg, Shahid Mahmood Baig, Muhammad Ansar, Peter Nürnberg, John B. Vincent, Michael R. Speicher, Pierre Gönczy, Christian Windpassinger	2014	50
11	Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family Human Genetics ·Asif Mir, Kumudesh Sritharan, Kirti Mittal, Nasim Vasli, Carolina Araujo-Sousa, Talal Jamil, Muhammad Rafiq, Zubair Anwar, Anna Mikhailov, Sobiah Rauf, Huda Mahmood, Abdul Shakoor, Sabir Ali, Joyce So, Farooq Naeem, Muhammad Ayub, John B. Vincent	2014	17
12	A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient Orphanet Journal of Rare Diseases ·Taimoor I. Sheikh, Kirti Mittal, Mary Willis, John B. Vincent	2013	20
13	Quantitative leukocyte BDNF promoter methylation analysis in bipolar disorder International Journal of Bipolar Disorders ·John S. Strauss, Tarang Khare, Vincenzo De Luca, Richie Jeremian, James L. Kennedy, John B. Vincent, Artūras Petronis	2013	13
14	A multi-tissue analysis identifies HLA complex group 9 gene methylation differences in bipolar disorder Molecular Psychiatry ·Zachary Kaminsky, Mamoru Tochigi, Pengxiang Jia, Mrinal Pal, Jonathan Mill, Angel Hoi Wan Kwan, Ilya Ioshikhes, John B. Vincent, James L. Kennedy, John S. Strauss, Shraddha Pai, S-C Wang, Artūras Petronis	2011	105
15	Replicated association of the NR4A3 gene with smoking behaviour in schizophrenia and in bipolar disorder Genes Brain & Behavior ·Gabriela Novak, Clement C. Zai, M. Mirkhani, Sajid A. Shaikh, John B. Vincent, Herbert Y. Meltzer, Jeffrey A. Lieberman, John S. Strauss, Daniel Lévesque, James L. Kennedy, Bernard Le Foll	2010	20
16	Population-based linkage analysis of schizophrenia and bipolar case–control cohorts identifies a potential susceptibility locus on 19q13 Molecular Psychiatry ·Clyde Francks, Federica Tozzi, Anne Farmer, John B. Vincent, Dan Rujescu, David St Clair, Pierandrea Muglia	2008	36
17	A translocation t(6;7)(p11–p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints Psychiatric Genetics ·John B. Vincent, Sanaa Choufani, Shin‐ichi Horike, Beata Stachowiak, Martin Li, F. J. Dill, Christian R. Marshall, Monica Hrynchak, Elizabeth Pewsey, Kennedy C. Ukadike, Jan M. Friedman, Anand K. Srivastava, Stephen W. Scherer	2008	11
18	A role for common fragile site induction in amplification of human oncogenes Cancer Cell ·Asaf Hellman, Eitan Zlotorynski, Stephen W. Scherer, Joseph Cheung, John B. Vincent, Jeremy C. Smith, Luba Trakhtenbrot, Batsheva Kerem	2002	240
19	Analysis of genome-wide CAG/CTG repeats, and at SEF2-1B and ERDA1 in schizophrenia and bipolar affective disorder Molecular Psychiatry ·John B. Vincent, Artūras Petronis, Emily Strong, Sagar V. Parikh, Herbert Y. Meltzer, Jeffrey A. Lieberman, James L. Kennedy	1999	26
20	Molecular and Cytogenetic Investigations of the Fragile X Region Including the Frax A and Frax E CGG Trinucleotide Repeat Sequences in Families Multiplex for Autism and Related Phenotypes Human Heredity ·H.M.D. Gliding, PF Bolton, John B. Vincent, Georg Melmer, Michael Rutter	1997	12

About John B. Vincent

John B. Vincent is a scholar working on Genetics, Biological Psychiatry, Cognitive Neuroscience, Cellular and Molecular Neuroscience and Psychiatry and Mental health, having authored 126 papers that have together received 4.4k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (54 papers), Genomic variations and chromosomal abnormalities (23 papers), Autism Spectrum Disorder Research (20 papers), Genomics and Rare Diseases (16 papers), Bipolar Disorder and Treatment (10 papers), Genetic Associations and Epidemiology (8 papers), Epigenetics and DNA Methylation (8 papers) and Genetic Neurodegenerative Diseases (8 papers). The work is most often cited by research in Genetics (1.7k citations), Biological Psychiatry (108 citations), Molecular Biology (1.9k citations), Cognitive Neuroscience (514 citations) and Cellular and Molecular Neuroscience (471 citations). John B. Vincent has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Muhammad Ayub, Stephen W. Scherer, James L. Kennedy, Abdul Noor, Hugh Gurling, Mark A. Ditmer, Leland K. Werden, George D. Weiblen, Christian Windpassinger and John S. Strauss. Their work appears in journals such as The American Journal of Human Genetics, Psychiatric Genetics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Human Molecular Genetics and Molecular Psychiatry.

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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