Victor A. David

4.1k total citations
72 papers, 2.4k citations indexed

About

Victor A. David is a scholar working on Genetics, Molecular Biology and Ecology. According to data from OpenAlex, Victor A. David has authored 72 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 32 papers in Molecular Biology and 12 papers in Ecology. Recurrent topics in Victor A. David's work include Genetic diversity and population structure (16 papers), Genetic and phenotypic traits in livestock (8 papers) and melanin and skin pigmentation (8 papers). Victor A. David is often cited by papers focused on Genetic diversity and population structure (16 papers), Genetic and phenotypic traits in livestock (8 papers) and melanin and skin pigmentation (8 papers). Victor A. David collaborates with scholars based in United States, Brazil and Russia. Victor A. David's co-authors include Marilyn Menotti‐Raymond, Stephen J. O’Brien, Alejandro A. Schäffer, Leslie A. Lyons, Eduardo Eizirik, Warren E. Johnson, Stephen J. O’Brien, Steven S. Hannah, Kristina Narfström and Alan H. Deutch and has published in prestigious journals such as PLoS ONE, Current Biology and Genetics.

In The Last Decade

Victor A. David

71 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Victor A. David United States 28 1.3k 881 748 218 154 72 2.4k
Khalid Shakir United States 2 1.8k 1.4× 2.1k 2.4× 243 0.3× 193 0.9× 211 1.4× 2 4.3k
David Roazen United States 2 1.8k 1.4× 2.1k 2.3× 242 0.3× 181 0.8× 210 1.4× 2 4.3k
Ami Levy‐Moonshine United States 5 1.9k 1.5× 2.2k 2.5× 253 0.3× 188 0.9× 221 1.4× 5 4.5k
Jess Shen Canada 4 1.1k 0.8× 658 0.7× 301 0.4× 119 0.5× 205 1.3× 7 2.1k
Mary J. O’Connell United States 27 563 0.4× 1.4k 1.6× 339 0.5× 71 0.3× 291 1.9× 99 2.7k
Laure Ségurel France 22 1.5k 1.1× 997 1.1× 179 0.2× 37 0.2× 155 1.0× 36 2.7k
Gabriella Lindgren Sweden 26 1.1k 0.9× 386 0.4× 221 0.3× 336 1.5× 260 1.7× 94 2.1k
Gabriel Renaud United States 21 894 0.7× 1.2k 1.4× 215 0.3× 102 0.5× 44 0.3× 43 2.6k
Danika L. Bannasch United States 32 1.2k 0.9× 1.5k 1.7× 186 0.2× 198 0.9× 92 0.6× 106 3.3k
Isaäc J. Nijman Netherlands 36 1.9k 1.4× 2.6k 3.0× 299 0.4× 384 1.8× 179 1.2× 81 5.1k

Countries citing papers authored by Victor A. David

Since Specialization
Citations

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

Fields of papers citing papers by Victor A. David

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Victor A. David. 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 Victor A. David. The network helps show where Victor A. David may publish in the future.

Co-authorship network of co-authors of Victor A. David

This figure shows the co-authorship network connecting the top 25 collaborators of Victor A. David. A scholar is included among the top collaborators of Victor A. David 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 Victor A. David. Victor A. David is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Toyoda, Yu, Sung Kweon Cho, Velibor Tasić, et al.. (2023). Identification of a dysfunctional exon-skipping splice variant in GLUT9/SLC2A9 causal for renal hypouricemia type 2. Frontiers in Genetics. 13. 1048330–1048330. 6 indexed citations
2.
David, Victor A., Luciana S. Wermelinger, Paulo Antônio de Souza Mourão, et al.. (2023). rJararacin, a recombinant disintegrin from Bothrops jararaca venom: Exploring its effects on hemostasis and thrombosis. Archives of Biochemistry and Biophysics. 738. 109557–109557. 3 indexed citations
3.
Costa, Priscila Ribas de Farias, et al.. (2023). Thiols as a marker of inflammatory bowel disease activity: a systematic review. BMC Gastroenterology. 23(1). 94–94. 1 indexed citations
4.
Yoon, Jaeho, Raúl E. Cachau, Victor A. David, et al.. (2021). Characterization of a Compound Heterozygous SLC2A9 Mutation That Causes Hypouricemia. Biomedicines. 9(9). 1172–1172. 4 indexed citations
5.
Levy, Rebecca V., Kimberly J. Reidy, Thu H. Le, et al.. (2021). Association of GSTM1 Deletion With Progression of CKD in Children: Findings From the Chronic Kidney Disease in Children (CKiD) Study. American Journal of Kidney Diseases. 80(1). 79–86. 5 indexed citations
6.
Balmer, Lois, Caroline A. O’Leary, Marilyn Menotti‐Raymond, et al.. (2020). Mapping of Diabetes Susceptibility Loci in a Domestic Cat Breed with an Unusually High Incidence of Diabetes Mellitus. Genes. 11(11). 1369–1369. 5 indexed citations
7.
Winkler, Cheryl A., et al.. (2020). Maternal variants within the apolipoprotein L1 gene are associated with preeclampsia in a South African cohort of African ancestry. European Journal of Obstetrics & Gynecology and Reproductive Biology. 246. 129–133. 19 indexed citations
8.
Bhimma, Rajendra, Victor A. David, Hoosen Coovadia, et al.. (2018). NPHS2 V260E Is a Frequent Cause of Steroid-Resistant Nephrotic Syndrome in Black South African Children. Kidney International Reports. 3(6). 1354–1362. 14 indexed citations
9.
Limou, Sophie, George W. Nelson, Laurence Lecordier, et al.. (2015). Sequencing rare and common APOL1 coding variants to determine kidney disease risk. Kidney International. 88(4). 754–763. 22 indexed citations
10.
Spencer, Peter B. S., Andrey A. Yurchenko, Victor A. David, et al.. (2015). The Population Origins and Expansion of Feral Cats in Australia. Journal of Heredity. 107(2). 104–114. 19 indexed citations
11.
Richards, Vincent P., Thomas W. Greig, Patricia A. Fair, et al.. (2013). Patterns of Population Structure for Inshore Bottlenose Dolphins along the Eastern United States. Journal of Heredity. 104(6). 765–778. 23 indexed citations
12.
Menotti‐Raymond, Marilyn, Victor A. David, B. S. Weir, & Stephen J. O’Brien. (2012). A Population Genetic Database of Cat Breeds Developed in Coordination with a Domestic Cat STR Multiplex*. Journal of Forensic Sciences. 57(3). 596–601. 11 indexed citations
13.
Ishida, Yasuko, Tarás K. Oleksyk, Nicholas J. Georgiadis, et al.. (2011). Reconciling Apparent Conflicts between Mitochondrial and Nuclear Phylogenies in African Elephants. PLoS ONE. 6(6). e20642–e20642. 43 indexed citations
14.
15.
Menotti‐Raymond, Marilyn, Victor A. David, Solveig M.V. Pflueger, et al.. (2007). Patterns of molecular genetic variation among cat breeds. Genomics. 91(1). 1–11. 59 indexed citations
16.
Wildt, David E., Russell A. Mittermeier, Susie Ellis, et al.. (2006). Giant Pandas. Cambridge University Press eBooks. 26 indexed citations
17.
Ishida, Yasuko, Victor A. David, Eduardo Eizirik, et al.. (2006). A homozygous single-base deletion in MLPH causes the dilute coat color phenotype in the domestic cat. Genomics. 88(6). 698–705. 82 indexed citations
18.
Murphy, William J., Brian W. Davis, Victor A. David, et al.. (2006). A 1.5-Mb-resolution radiation hybrid map of the cat genome and comparative analysis with the canine and human genomes. Genomics. 89(2). 189–196. 45 indexed citations
19.
Fyfe, John C., Marilyn Menotti‐Raymond, Victor A. David, et al.. (2006). An ~140-kb deletion associated with feline spinal muscular atrophy implies an essentialLIX1function for motor neuron survival. Genome Research. 16(9). 1084–1090. 32 indexed citations
20.
David, Victor A. & Alan H. Deutch. (1992). Detection of bovine αs1‐casein genomic variants using the allele‐specific polymerase chain reaction. Animal Genetics. 23(5). 425–429. 21 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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