John Wei

6.2k citations

17 papers · 884 indexed · h-index 13

Impact in

Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Cognitive Neuroscience top 10%
- Autism Spectrum Disorder Research

Papers in ⓘ

Genetics 15
- Genomic variations and chromosomal abnormalities 14
- Genomics and Rare Diseases 6
- Genetics and Neurodevelopmental Disorders 3
- Inflammatory Bowel Disease 2
Pediatrics, Perinatology and Child Health 5
- Prenatal Screening and Diagnostics 4

Co-authors: Stephen W. Scherer (16 shared papers)Christian R. Marshall (6 shared papers)Bhooma Thiruvahindrapuram (9 shared papers)Matthew E. Hurles (2 shared papers)Muhammad Rafiq (2 shared papers)Lars Feuk (2 shared papers)Charles Lee (2 shared papers)Jeffrey R. MacDonald (2 shared papers)
Journals: American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2 papers)Genome Medicine (1 paper)Biological Psychiatry (1 paper)Autism Research (1 paper)Nature Genetics (1 paper)
Partner nations: Canada United Kingdom United States

In The Last Decade

John Wei

17 papers receiving 869 citations

Peers

Countries citing papers authored by John Wei

Since Specialization

Citations

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

Fields of papers citing papers by John Wei

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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17 of 17 papers shown

#	Work
1	Towards a comprehensive structural variation map of an individual human genome Genome biology ·Andy Wing Chun Pang, Jeffrey R. MacDonald, Dalila Pinto, John Wei, Muhammad Rafiq, Donald F. Conrad, Hansoo Park, Matthew E. Hurles, Charles Lee, J. Craig Venter, Ewen F. Kirkness, Samuel Lévy, Lars Feuk, Stephen W. Scherer	2010	214
2	A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder G3 Genes Genomes Genetics ·Aparna Prasad, Daniele Merico, Bhooma Thiruvahindrapuram, John Wei, Anath C. Lionel, Daisuke Sato, Jessica Rickaby, Chao Lu, Péter Szatmári, Wendy Roberts, Bridget A. Fernandez, Christian R. Marshall, Eli Hatchwell, Peggy S. Eis, Stephen W. Scherer	2012	145
3	Genome assembly comparison identifies structural variants in the human genome Nature Genetics ·Razi Khaja, Junjun Zhang, Jeffrey R. MacDonald, Yongshu He, Ann M. Joseph‐George, John Wei, Muhammad Rafiq, Qian Cheng, Mary Shago, Lorena Pantano, Hiroyuki Aburatani, Keith Jones, Richard Redon, Matthew E. Hurles, Lluı́s Armengol, Xavier Estivill, Richard Mural, Charles Lee, Stephen W. Scherer, Lars Feuk	2006	113
4	Clinically relevant copy number variations detected in cerebral palsy Nature Communications ·Maryam Oskoui, Matthew J. Gazzellone, Bhooma Thiruvahindrapuram, Mehdi Zarrei, John Andersen, John Wei, Zhuozhi Wang, Richard F. Wintle, Christian R. Marshall, Ronald D. Cohn, Rosanna Weksberg, Dimitri J. Stavropoulos, Darcy Fehlings, Michael Shevell, Stephen W. Scherer	2015	103
5	Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Abdul Noor, Anath C. Lionel, Sarah Cohen‐Woods, Narges Moghimi, James Rucker, Alanna Fennell, Bhooma Thiruvahindrapuram, Liana Kaufman, Bryan Degagne, John Wei, Sagar V. Parikh, Pierandrea Muglia, Julia Forte, Stephen W. Scherer, James L. Kennedy, Wei Xu, Peter McGuffin, Anne Farmer, John S. Strauss, John B. Vincent	2014	61
6	Copy Number Variable MicroRNAs in Schizophrenia and Their Neurodevelopmental Gene Targets Biological Psychiatry ·W. David Warnica, Daniele Merico, Gregory Costain, Simon E. Alfred, John Wei, Christian R. Marshall, Stephen W. Scherer, Anne S. Bassett	2014	52
7	Copy number variation in Han Chinese individuals with autism spectrum disorder Journal of Neurodevelopmental Disorders ·Matthew J. Gazzellone, Xue Zhou, Anath C. Lionel, Mohammed Uddin, Bhooma Thiruvahindrapuram, Shuang Liang, Caihong Sun, Jia Wang, Mingyang Zou, Kristiina Tammimies, Susan Walker, Thanuja Selvanayagam, John Wei, Zhuozhi Wang, Lijie Wu, Stephen W. Scherer	2014	44
8	Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia Genome Medicine ·Chelsea Lowther, Daniele Merico, Gregory Costain, Jack Waserman, Kerry Boyd, Abdul Noor, Marsha Speevak, Dimitri J. Stavropoulos, John Wei, Anath C. Lionel, Christian R. Marshall, Stephen W. Scherer, Anne S. Bassett	2017	24
9	A genotype resource for postmortem brain samples from the Autism Tissue Program Autism Research ·Richard F. Wintle, Anath C. Lionel, Pingzhao Hu, Stephen D. Ginsberg, Dalila Pinto, Bhooma Thiruvahindrapduram, John Wei, Christian R. Marshall, Jane Pickett, Edwin H. Cook, Stephen W. Scherer	2011	21
10	Evolutionary implications of inversions that have caused intra-strand parity in DNA BMC Genomics ·K. Okamura, John Wei, Stephen W. Scherer	2007	21
11	Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders Twin Research and Human Genetics ·Sofia Stamouli, Britt‐Marie Anderlid, Charlotte Willfors, Bhooma Thiruvahindrapuram, John Wei, Steve Berggren, Ann Nordgren, Stephen W. Scherer, Paul Lichtenstein, Kristiina Tammimies, Sven Bölte	2018	19
12	Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease PLoS ONE ·Svetlana Frenkel, Çharles N. Bernstein, Michael Sargent, Qin Kuang, Wenxin Jiang, John Wei, Bhooma Thiruvahindrapuram, Elizabeth Spriggs, Stephen W. Scherer, Pingzhao Hu	2019	18
13	Genomic imbalances in the placenta are associated with poor fetal growth Molecular Medicine ·Giulia Gobbo, Yue Yin, Sanaa Choufani, Emma Butcher, John Wei, Evica Rajcan‐Separovic, Hayley Bos, Peter von Dadelszen, Rosanna Weksberg, Wendy P. Robinson, Ryan K. C. Yuen	2021	18
14	Copy number variation in fetal alcohol spectrum disorder Biochemistry and Cell Biology ·Mehdi Zarrei, Geoffrey G. Hicks, James N. Reynolds, Bhooma Thiruvahindrapuram, Worrawat Engchuan, Molly Pind, Sylvia Lamoureux, John Wei, Zhouzhi Wang, Christian R. Marshall, Richard F. Wintle, Albert E. Chudley, Stephen W. Scherer	2018	12
15	Rare copy number variation in extremely impulsively violent males Genes Brain & Behavior ·Jan Vevera, Mehdi Zarrei, Hana Hartmannová, Ivana Jedličková, Dita Mušálková, Anna Přistoupilová, Petra Oliveriusová, Helena Trešlová, Lenka Nosková, Kateřina Hodaňová, Viktor Stránecký, Václav Jiřička, Marek Preiss, Kateřina Příhodová, Jana Šaligová, John Wei, Marc Woodbury‐Smith, Anthony J. Bleyer, Stephen W. Scherer, Stanislav Kmoch	2018	10
16	Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Marc Woodbury‐Smith, Mehdi Zarrei, John Wei, Bhooma Thiruvahindrapuram, Irene O’Connor, Andrew D. Paterson, Ryan K. C. Yuen, Jila Dastan, Dimitri J. Stavropoulos, Jennifer Howe, Ann Thompson, Morgan Parlier, Bridget A. Fernandez, Joseph Piven, Evdokia Anagnostou, Stephen W. Scherer, Veronica J. Vieland, Péter Szatmári	2020	8
17	Genome-Wide Analysis Identifies Rare Copy Number Variations Associated with Inflammatory Bowel Disease Gastroenterology ·Svetlana Frenkel, Michael Sargent, Qin Kuang, John Wei, Bhooma Thiruvahindrapuram, Elizabeth Spriggs, Stephen W. Scherer, Çharles N. Bernstein, Pingzhao Hu	2017	1

About John Wei

John Wei is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Cognitive Neuroscience, Clinical Biochemistry and Obstetrics and Gynecology, having authored 17 papers that have together received 884 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (14 papers), Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Autism Spectrum Disorder Research (3 papers), Chromosomal and Genetic Variations (3 papers), Inflammatory Bowel Disease (2 papers) and Genomics and Phylogenetic Studies (2 papers). The work is most often cited by research in Genetics (563 citations), Cognitive Neuroscience (141 citations), Pediatrics, Perinatology and Child Health (126 citations), Molecular Biology (422 citations) and Psychiatry and Mental health (90 citations). John Wei has collaborated with scholars based in Canada, United Kingdom and United States. Frequent co-authors include Stephen W. Scherer, Christian R. Marshall, Bhooma Thiruvahindrapuram, Matthew E. Hurles, Muhammad Rafiq, Lars Feuk, Charles Lee, Jeffrey R. MacDonald, Anath C. Lionel and Daniele Merico. Their work appears in journals such as American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Genome Medicine, Biological Psychiatry, Autism Research and Nature 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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