Andrei Verner

13.4k total citations
19 papers, 1.4k citations indexed

About

Andrei Verner is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Andrei Verner has authored 19 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Surgery. Recurrent topics in Andrei Verner's work include Genetic Syndromes and Imprinting (4 papers), Genomics and Chromatin Dynamics (4 papers) and Asthma and respiratory diseases (3 papers). Andrei Verner is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Genomics and Chromatin Dynamics (4 papers) and Asthma and respiratory diseases (3 papers). Andrei Verner collaborates with scholars based in Canada, United States and Costa Rica. Andrei Verner's co-authors include Guy A. Rouleau, Thomas J. Hudson, Haiheng Dong, Yu Tian Wang, Katéri Brisebois, Michel Vanasse, Anne Lortie, Patrick Cossette, Lionel Carmant and Jean‐Marc Saint‐Hilaire and has published in prestigious journals such as Nature Genetics, Genetics and The American Journal of Human Genetics.

In The Last Decade

Andrei Verner

19 papers receiving 1.4k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Andrei Verner Canada 17 670 507 287 269 265 19 1.4k
Alison Gardner Australia 17 799 1.2× 569 1.1× 339 1.2× 143 0.5× 225 0.8× 30 1.6k
Shin‐ichiro Hamano Japan 19 340 0.5× 246 0.5× 612 2.1× 90 0.3× 329 1.2× 111 1.3k
Junko Nakayama Japan 22 427 0.6× 330 0.7× 392 1.4× 77 0.3× 245 0.9× 53 1.3k
Alex R. Paciorkowski United States 21 630 0.9× 669 1.3× 270 0.9× 60 0.2× 161 0.6× 49 1.4k
Tomohide Goto Japan 18 602 0.9× 165 0.3× 125 0.4× 71 0.3× 328 1.2× 67 1.3k
Christian Korff Switzerland 24 307 0.5× 307 0.6× 638 2.2× 51 0.2× 322 1.2× 87 1.3k
Fang He China 20 623 0.9× 410 0.8× 231 0.8× 66 0.2× 191 0.7× 59 1.3k
Syed Hosain United States 15 288 0.4× 194 0.4× 345 1.2× 47 0.2× 150 0.6× 24 1.0k
Lana M. Olson United States 18 1.2k 1.7× 552 1.1× 77 0.3× 148 0.6× 70 0.3× 25 3.4k
Michael Freilinger Austria 19 447 0.7× 206 0.4× 223 0.8× 45 0.2× 95 0.4× 42 1.2k

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-authorship network of co-authors of Andrei Verner

This figure shows the co-authorship network connecting the top 25 collaborators of Andrei Verner. A scholar is included among the top collaborators of Andrei Verner based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrei Verner. Andrei Verner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Hersh, Craig P., Lydiana Ávila, Sarah L. Lake, et al.. (2006). Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica. Thorax. 62(3). 224–230. 15 indexed citations
2.
Raby, Benjamin A., Manuel E. Soto-Quirós, Lydiana Ávila, et al.. (2006). Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica. Human Molecular Genetics. 16(3). 243–253. 22 indexed citations
3.
Celedón, Juan C., Manuel E. Soto-Quirós, Lydiana Ávila, et al.. (2006). Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica. Human Genetics. 120(5). 691–699. 17 indexed citations
4.
Worgan, Lisa, et al.. (2005). Spectrum of mutations inmutmethylmalonic acidemia and identification of a common Hispanic mutation and haplotype. Human Mutation. 27(1). 31–43. 90 indexed citations
5.
Montpetit, Alexandre, et al.. (2004). An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22. Human Genetics. 116(3). 167–171. 27 indexed citations
6.
Pato, Carlos N., Michele T. Pato, Andrew Kirby, et al.. (2004). 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. 127B(1). 30–34. 29 indexed citations
7.
Pastinen, Tomi, Robert Sladek, Scott Gurd, et al.. (2004). A survey of genetic and epigenetic variation affecting human gene expression. Physiological Genomics. 16(2). 184–193. 209 indexed citations
8.
Couture, Patrick, Alain Houde, Ann-Marie Paradis, et al.. (2003). The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians. Molecular Genetics and Metabolism. 81(2). 140–143. 19 indexed citations
9.
Mira, Marcelo Távora, Alexandre Alcaïs, Nguyen Van Thuc, et al.. (2003). Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population. Nature Genetics. 33(3). 412–415. 142 indexed citations
10.
Cossette, Patrick, Lidong Liu, Katéri Brisebois, et al.. (2002). Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy. Nature Genetics. 31(2). 184–189. 449 indexed citations
11.
Héon, Elise, Andrew D. Paterson, Michael Fraser, et al.. (2001). A Progressive Autosomal Recessive Cataract Locus Maps to Chromosome 9q13-q22. The American Journal of Human Genetics. 68(3). 772–777. 45 indexed citations
12.
Seyda, Agnieszka, Robert F. Newbold, Thomas J. Hudson, et al.. (2001). A Novel Syndrome Affecting Multiple Mitochondrial Functions, Located by Microcell-Mediated Transfer to Chromosome 2p14-2p13. The American Journal of Human Genetics. 68(2). 386–396. 57 indexed citations
13.
Désautels, Alex, et al.. (2001). Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q. The American Journal of Human Genetics. 69(6). 1266–1270. 181 indexed citations
14.
Bétard, Christine, Andrée Rasquin‐Weber, Carl G. Brewer, et al.. (2000). 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. 67(1). 222–228. 26 indexed citations
15.
Casa‐Esperón, Elena de la, et al.. (2000). Sex-of-Offspring-Specific Transmission Ratio Distortion on Mouse Chromosome X. Genetics. 154(1). 343–350. 16 indexed citations
16.
Villena, Fernando Pardo‐Manuel de, Elena de la Casa‐Esperón, Andrei Verner, & Kenneth Morgan. (1999). The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om. Mammalian Genome. 10(5). 492–497. 19 indexed citations
17.
Villena, Fernando Pardo‐Manuel de, et al.. (1997). Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal “DDK syndrome” genes are linked. Mammalian Genome. 8(9). 642–646. 37 indexed citations
18.
Villena, Fernando Pardo‐Manuel de, M. E. N. Fonseca, Anna K. Naumova, et al.. (1996). Transmission-Ratio Distortion Through F1 Females at Chromosome 11 Loci Linked to Om in the Mouse DDK Syndrome. Genetics. 142(4). 1299–1304. 22 indexed citations
19.
Naumova, Anna K., Lynne M. Bird, M. E. N. Fonseca, et al.. (1995). Transmission‐ratio distortion of X chromosomes among male offspring of females with skewed X‐inactivation. Developmental Genetics. 17(3). 198–205. 22 indexed citations

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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