Davit Babikyan

583 total citations
7 papers, 231 citations indexed

About

Davit Babikyan is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Davit Babikyan has authored 7 papers receiving a total of 231 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Davit Babikyan's work include BRCA gene mutations in cancer (4 papers), Genomics and Rare Diseases (3 papers) and Genetic factors in colorectal cancer (2 papers). Davit Babikyan is often cited by papers focused on BRCA gene mutations in cancer (4 papers), Genomics and Rare Diseases (3 papers) and Genetic factors in colorectal cancer (2 papers). Davit Babikyan collaborates with scholars based in United States, Armenia and France. Davit Babikyan's co-authors include Sean V. Tavtigian, Maxime Vallée, Fabienne Lesueur, John L. Hopper, Fergus J. Couch, Amanda Gammon, David E. Goldgar, David H. Cribbs, Ted M. Ross and Anahit Ghochikyan and has published in prestigious journals such as Journal of Clinical Oncology, European Journal of Immunology and Breast Cancer Research.

In The Last Decade

Davit Babikyan

7 papers receiving 230 citations

Peers

Countries citing papers authored by Davit Babikyan

Since Specialization

Citations

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

Fields of papers citing papers by Davit Babikyan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Davit Babikyan

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Germline mutational spectrum in Armenian breast cancer patients suspected of hereditary breast and ovarian cancer 2021 ·Human Genome Variation ·(unknown), Davit Babikyan, (unknown), (unknown), (unknown), (unknown), Tamara Sarkisian	7
2	A novel variant of C12orf4 in a consanguineous Armenian family confirms the etiology of autosomal recessive intellectual disability type 66 with delineation of the phenotype 2019 ·Molecular Genetics & Genomic Medicine ·Miroslava Hančárová, Davit Babikyan, Šárka Bendová, (unknown), Darina Prchalová, (unknown), Viktor Stránecký, Tamara Sarkisian, Zdeněk Sedláček	4
3	Comprehensive analysis of mutations in the MEFV gene reveal that the location and not the substitution type determines symptom severity in FMF 2017 ·Molecular Genetics & Genomic Medicine ·(unknown), Davit Babikyan, (unknown), Hasmik Hayrapetyan, (unknown), (unknown), Tamara Sarkisian	12
4	Rare, evolutionarily unlikely missense substitutions in CHEK2contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study 2011 ·Breast Cancer Research ·Florence Le Calvez‐Kelm, Fabienne Lesueur, Francesca Damiola, Maxime Vallée, Catherine Voegele, Davit Babikyan, Geoffroy Durand, Nathalie Forey, Sandrine McKay‐Chopin, Nivonirina Robinot, Tú Nguyen‐Dumont, Alun Thomas, Graham Byrnes, (unknown), John L. Hopper, Melissa C. Southey, Irene L. Andrulis, Esther M. John, Sean V. Tavtigian	54
5	Classification of missense substitutions in the BRCA genes: A database dedicated to Ex-UVs 2011 ·Human Mutation ·Maxime Vallée, (unknown), (unknown), Davit Babikyan, Fabienne Lesueur, Amanda Gammon, David E. Goldgar, Fergus J. Couch, Sean V. Tavtigian	51
6	Clinical Classification ofBRCA1andBRCA2DNA Sequence Variants: The Value of Cytokeratin Profiles and Evolutionary Analysis—A Report From the kConFab Investigators 2008 ·Journal of Clinical Oncology ·Amanda B. Spurdle, Sunil R. Lakhani, Sue Healey, Suzanne Parry, Leonard Da Silva, Ross I. Brinkworth, John L. Hopper, Melissa A. Brown, Davit Babikyan, Georgia Chenevix‐Trench, Sean V. Tavtigian, David E. Goldgar	53
7	Generation and characterization of the humoral immune response to DNA immunization with a chimeric β‐amyloid‐interleukin‐4 minigene 2003 ·European Journal of Immunology ·Anahit Ghochikyan, Vitaly Vasilevko, Irina Petrushina, Nina Movsesyan, Davit Babikyan, (unknown), (unknown), Ted M. Ross, Elizabeth Head, David H. Cribbs, Michael G. Agadjanyan	50

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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