Andrei Verner

13.4k citations

19 papers · 1.4k indexed · h-index 17

Impact in

Psychiatry and Mental health top 5%
- Epilepsy research and treatment
Genetics top 5%
- Genetics and Neurodevelopmental Disorders

Papers in ⓘ

Genetics 9
- Genetic Syndromes and Imprinting 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Genetic Associations and Epidemiology 2
Clinical Biochemistry 2
- Metabolism and Genetic Disorders 2

Co-authors: Guy A. Rouleau (2 shared papers)Thomas J. Hudson (10 shared papers)Jean‐Marc Saint‐Hilaire (1 shared paper)Patrick Cossette (1 shared paper)Katéri Brisebois (1 shared paper)Lionel Carmant (1 shared paper)Michel Vanasse (1 shared paper)Haiheng Dong (1 shared paper)
Journals: The American Journal of Human Genetics (4 papers)Nature Genetics (2 papers)Genetics (2 papers)Mammalian Genome (2 papers)Human Genetics (2 papers)
Partner nations: Canada United States Costa Rica

In The Last Decade

Andrei Verner

19 papers receiving 1.4k citations

Peers

Countries citing papers authored by Andrei Verner

Since Specialization

Citations

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

Fields of papers citing papers by Andrei Verner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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19 of 19 papers shown

#	Work
1	Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy Nature Genetics ·Patrick Cossette, Lidong Liu, Katéri Brisebois, Haiheng Dong, Anne Lortie, Michel Vanasse, Jean‐Marc Saint‐Hilaire, Lionel Carmant, Andrei Verner, Wei‐Yang Lu, Yu Tian Wang, Guy A. Rouleau	2002	449
2	A survey of genetic and epigenetic variation affecting human gene expression Physiological Genomics ·Tomi Pastinen, Robert Sladek, Scott Gurd, Alya’a Sammak, Bing Ge, Patricia Lepage, Karine J. Lavergne, Amélie Villeneuve, Tiffany Gaudin, Helena Brändström, Allon Beck, Andrei Verner, Jade Kingsley, Eef Harmsen, Damian Labuda, Kenneth Morgan, Marie‐Claude Vohl, Anna K. Naumova, Daniel Sinnett, Thomas J. Hudson	2004	209
3	Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q The American Journal of Human Genetics ·Alex Désautels, Gustavo Turecki, Jacques Montplaisir, Adolfo Sequeira, Andrei Verner, Guy A. Rouleau	2001	181
4	Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population Nature Genetics ·Marcelo Távora Mira, Alexandre Alcaïs, Nguyen Van Thuc, Vu Hong Thai, Nguyễn Thu Hương, Nguyen Ngoc Ba, Andrei Verner, Thomas J. Hudson, Laurent Abel, Erwin Schurr	2003	142
5	Spectrum of mutations inmutmethylmalonic acidemia and identification of a common Hispanic mutation and haplotype Human Mutation ·Lisa Worgan, Kirsten M. Niles, Jamie C. Tirone, Adam Hofmann, Andrei Verner, Alya’a Sammak, Terrence Kucic, Patricia Lepage, David S. Rosenblatt	2005	90
6	A Novel Syndrome Affecting Multiple Mitochondrial Functions, Located by Microcell-Mediated Transfer to Chromosome 2p14-2p13 The American Journal of Human Genetics ·Agnieszka Seyda, Robert F. Newbold, Thomas J. Hudson, Andrei Verner, Neviana MacKay, Susan Winter, Annette Feigenbaum, Suzann Malaney, Diego González‐Halphen, Andrew Cuthbert, Brian H. Robinson	2001	57
7	A Progressive Autosomal Recessive Cataract Locus Maps to Chromosome 9q13-q22 The American Journal of Human Genetics ·Elise Héon, Andrew D. Paterson, Michael Fraser, Gail Billingsley, Megan Priston, Aubin Balmer, Daniel F. Schorderet, Andrei Verner, Thomas J. Hudson, Francis L. Munier	2001	45
8	Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal “DDK syndrome” genes are linked Mammalian Genome ·Fernando Pardo‐Manuel de Villena, Anna K. Naumova, Andrei Verner, Wen-Hui Jin, Carmen Sapienza	1997	37
9	Genome‐wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: Fine mapping adds support on chromosomes 6 and 11 American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Carlos N. Pato, Michele T. Pato, Andrew Kirby, Tracey L. Petryshen, Helena Medeiros, Célia Barreto Carvalho, A. Macedo, A. Dourado, I. Coelho, J. Valente, M.J. Soares, Carlos Paz Ferreira, M. Lei, Andrei Verner, Thomas J. Hudson, Christopher P. Morley, James L. Kennedy, Maria Helena Pinto de Azevedo, Mark J. Daly, Pamela Sklar	2004	29
10	An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22 Human Genetics ·Thomas G. Saba, Alexandre Montpetit, Andrei Verner, Pierre Rioux, Thomas J. Hudson, R�gen Drouin, Christian A. Drouin	2004	27
11	Localization of a Recessive Gene for North American Indian Childhood Cirrhosis to Chromosome Region 16q22—and Identification of a Shared Haplotype The American Journal of Human Genetics ·Christine Bétard, Andrée Rasquin‐Weber, Carl G. Brewer, Éric Drouin, Suzanne Clark, Andrei Verner, Corinne Darmond-Zwaig, J.P. Fortin, Jocelyne Mercier, Pierre Chagnon, Takuya Fujiwara, Kenneth Morgan, Andréa Richter, Thomas J. Hudson, Grant A. Mitchell	2000	26
12	Transmission‐ratio distortion of X chromosomes among male offspring of females with skewed X‐inactivation Developmental Genetics ·Anna K. Naumova, Leonard Olien, Lynne M. Bird, C. Slamka, M. E. N. Fonseca, Andrei Verner, M. Wang, Mark Leppert, Kenneth Morgan, Carmen Sapienza	1995	22
13	Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica Human Molecular Genetics ·Benjamin A. Raby, Manuel E. Soto-Quirós, Lydiana Ávila, Stephen Lake, Amy Murphy, Catherine Liang, Eduardo Fournier, Mitzi Spesny, Jody Sylvia, Andrei Verner, Thomas J. Hudson, Barbara J. Klanderman, Nelson B. Freimer, Edwin K. Silverman, Juan C. Celedón	2006	22
14	Transmission-Ratio Distortion Through F1 Females at Chromosome 11 Loci Linked to Om in the Mouse DDK Syndrome Genetics ·Fernando Pardo‐Manuel de Villena, C. Slamka, M. E. N. Fonseca, Anna K. Naumova, Jean Paquette, P Pannunzio, Mark A. Smith, Andrei Verner, Kenneth Morgan, Carmen Sapienza	1996	22
15	The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians Molecular Genetics and Metabolism ·Marie‐Thérèse Berthier, Patrick Couture, Alain Houde, Ann-Marie Paradis, Alya’a Sammak, Andrei Verner, Jean-Pierre Deprés, Claude Gagné, Daniel Gaudet, Marie‐Claude Vohl	2003	19
16	The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om Mammalian Genome ·Fernando Pardo‐Manuel de Villena, Elena de la Casa‐Esperón, Andrei Verner, Kenneth Morgan	1999	19
17	Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica Human Genetics ·Juan C. Celedón, Manuel E. Soto-Quirós, Lydiana Ávila, Stephen Lake, Catherine Liang, Eduardo Fournier, Mitzi Spesny, Craig P. Hersh, Jody Sylvia, Thomas J. Hudson, Andrei Verner, Barbara J. Klanderman, Nelson B. Freimer, Edwin K. Silverman, Scott T. Weiss	2006	17
18	Sex-of-Offspring-Specific Transmission Ratio Distortion on Mouse Chromosome X Genetics ·Elena de la Casa‐Esperón, Fernando Pardo‐Manuel de Villena, Andrei Verner, Tammi L Briscoe, Jan Michel Malette, Michelle Rosa, Wen-Hui Jin, Carmen Sapienza	2000	16
19	Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica Thorax ·Craig P. Hersh, M. E Soto-Quiros, Lydiana Ávila, Sarah L. Lake, Chang‐seng Liang, Eduardo Fournier, Mitzi Spesny, J. S Sylvia, Ross Lazarus, Thomas J. Hudson, Andrei Verner, Barbara J. Klanderman, Nelson B. Freimer, Edwin K. Silverman, JC Celedon	2006	15

About Andrei Verner

Andrei Verner is a scholar working on Genetics, Clinical Biochemistry, Immunology and Allergy, Molecular Biology and Speech and Hearing, having authored 19 papers that have together received 1.4k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (4 papers), Genetic Syndromes and Imprinting (4 papers), Asthma and respiratory diseases (3 papers), Metabolism and Genetic Disorders (2 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Epigenetics and DNA Methylation (2 papers), Connexins and lens biology (2 papers) and Genetic Associations and Epidemiology (2 papers). The work is most often cited by research in Psychiatry and Mental health (287 citations), Genetics (507 citations), Clinical Biochemistry (120 citations), Cellular and Molecular Neuroscience (265 citations) and Neurology (172 citations). Andrei Verner has collaborated with scholars based in Canada, United States and Costa Rica. Frequent co-authors include Guy A. Rouleau, Thomas J. Hudson, Jean‐Marc Saint‐Hilaire, Patrick Cossette, Katéri Brisebois, Lionel Carmant, Michel Vanasse, Haiheng Dong, Anne Lortie and Lidong Liu. Their work appears in journals such as The American Journal of Human Genetics, Nature Genetics, Genetics, Mammalian Genome and Human 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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