Avinash Abhyankar

7.4k total citations
30 papers, 1.9k citations indexed

About

Avinash Abhyankar is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Avinash Abhyankar has authored 30 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 8 papers in Immunology. Recurrent topics in Avinash Abhyankar's work include Genomics and Rare Diseases (10 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Avinash Abhyankar is often cited by papers focused on Genomics and Rare Diseases (10 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Avinash Abhyankar collaborates with scholars based in United States, France and United Kingdom. Avinash Abhyankar's co-authors include Jean‐Laurent Casanova, Laurent Abel, Arnold Münnich, Patrick Nitschké, Agata Smogorzewska, Arleen D. Auerbach, Francis P. Lach, Emmanuelle Jouanguy, Capucine Pïcard and Minji Byun and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Avinash Abhyankar

30 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Avinash Abhyankar United States 20 959 650 358 223 186 30 1.9k
F. Yesim Demirci United States 25 843 0.9× 490 0.8× 467 1.3× 197 0.9× 136 0.7× 89 2.1k
Marc A. Schaub United States 8 1.5k 1.5× 1.1k 1.7× 302 0.8× 150 0.7× 132 0.7× 9 2.6k
Ann Nordgren Sweden 29 1.1k 1.2× 997 1.5× 144 0.4× 217 1.0× 116 0.6× 134 2.6k
Demetrios A. Arvanitis Greece 25 776 0.8× 231 0.4× 194 0.5× 124 0.6× 163 0.9× 63 1.7k
J F Bach France 18 795 0.8× 343 0.5× 631 1.8× 107 0.5× 147 0.8× 38 3.0k
Laurent Essioux Switzerland 18 600 0.6× 672 1.0× 170 0.5× 169 0.8× 101 0.5× 32 1.7k
Paola Forabosco Italy 23 453 0.5× 434 0.7× 317 0.9× 60 0.3× 102 0.5× 48 1.5k
G Grimber France 24 1.2k 1.2× 312 0.5× 233 0.7× 293 1.3× 234 1.3× 48 2.1k
Cinzia Pupilli Italy 26 420 0.4× 360 0.6× 716 2.0× 323 1.4× 199 1.1× 55 2.1k
Curtis Gumbs United States 20 1.3k 1.3× 543 0.8× 154 0.4× 289 1.3× 356 1.9× 45 2.7k

Countries citing papers authored by Avinash Abhyankar

Since Specialization
Citations

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

Fields of papers citing papers by Avinash Abhyankar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Avinash Abhyankar

This figure shows the co-authorship network connecting the top 25 collaborators of Avinash Abhyankar. A scholar is included among the top collaborators of Avinash Abhyankar 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 Avinash Abhyankar. Avinash Abhyankar 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.
Hays, Thomas, Rebecca Hernan, Ganga Krishnamurthy, et al.. (2023). Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease. Circulation Genomic and Precision Medicine. 16(5). 415–420. 11 indexed citations
2.
Kline, Jennie, Badri N. Vardarajan, Avinash Abhyankar, et al.. (2021). Embryonic lethal genetic variants and chromosomally normal pregnancy loss. Fertility and Sterility. 116(5). 1351–1358. 8 indexed citations
3.
Jobanputra, Vaidehi, Peter Andrews, Vanessa Felice, et al.. (2020). Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies. Journal of Molecular Diagnostics. 22(12). 1476–1481. 1 indexed citations
4.
Rickman, Kimberly A., Francis P. Lach, Sunandini Sridhar, et al.. (2020). Distinct roles of BRCA2 in replication fork protection in response to hydroxyurea and DNA interstrand cross-links. Genes & Development. 34(11-12). 832–846. 50 indexed citations
5.
Felice, Vanessa, Avinash Abhyankar, & Vaidehi Jobanputra. (2018). Prenatal Diagnosis by Whole Exome Sequencing in Fetuses with Ultrasound Abnormalities. Methods in molecular biology. 1885. 267–285. 3 indexed citations
6.
Abhyankar, Avinash, Michelle F. Lamendola-Essel, Kelly Brennan, et al.. (2017). Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency. Clinical Case Reports. 6(1). 200–205. 13 indexed citations
7.
Freudenberg‐Hua, Yun, Wentian Li, Avinash Abhyankar, et al.. (2016). Differential burden of rare protein truncating variants in Alzheimer’s disease patients compared to centenarians. Human Molecular Genetics. 25(14). ddw150–ddw150. 8 indexed citations
8.
Rickman, Kimberly A., Francis P. Lach, Avinash Abhyankar, et al.. (2015). Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia. Cell Reports. 12(1). 35–41. 111 indexed citations
9.
Kong, Xiao‐Fei, Aziz Bousfiha, Yuval Itan, et al.. (2013). A Novel Homozygous p.R1105X Mutation of the AP4E1 Gene in Twins with Hereditary Spastic Paraplegia and Mycobacterial Disease. PLoS ONE. 8(3). e58286–e58286. 27 indexed citations
10.
Itan, Yuval, Shen‐Ying Zhang, Guillaume Vogt, et al.. (2013). The human gene connectome as a map of short cuts for morbid allele discovery. Proceedings of the National Academy of Sciences. 110(14). 5558–5563. 46 indexed citations
11.
Bolze, Alexandre, Avinash Abhyankar, Audrey V. Grant, et al.. (2012). A Mild Form of SLC29A3 Disorder: A Frameshift Deletion Leads to the Paradoxical Translation of an Otherwise Noncoding mRNA Splice Variant. PLoS ONE. 7(1). e29708–e29708. 44 indexed citations
12.
Michot, Caroline, Carine Le Goff, Alice Goldenberg, et al.. (2012). Exome Sequencing Identifies PDE4D Mutations as Another Cause of Acrodysostosis. The American Journal of Human Genetics. 90(4). 740–745. 84 indexed citations
13.
Créquer, Amandine, Capucine Pïcard, Étienne Patin, et al.. (2012). Inherited MST1 Deficiency Underlies Susceptibility to EV-HPV Infections. PLoS ONE. 7(8). e44010–e44010. 92 indexed citations
14.
Barcia, Giulia, Matthew R. Fleming, Valeswara‐Rao Gazula, et al.. (2012). De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy. Nature Genetics. 44(11). 1255–1259. 335 indexed citations
15.
Goff, Carine Le, Clémentine Mahaut, Avinash Abhyankar, et al.. (2011). Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome. Nature Genetics. 44(1). 85–88. 117 indexed citations
16.
Bolze, Alexandre, Minji Byun, David McDonald, et al.. (2010). Whole-Exome-Sequencing-Based Discovery of Human FADD Deficiency. The American Journal of Human Genetics. 87(6). 873–881. 118 indexed citations
17.
Abhyankar, Avinash, Hee-Bok Park, Giancarlo Tonolo, & Holger Luthman. (2009). Comparative Sequence Analysis of the Non-Protein-Coding Mitochondrial DNA of Inbred Rat Strains. PLoS ONE. 4(12). e8148–e8148. 15 indexed citations
18.
Tonolo, Giancarlo, Mario Velussi, Enrico Brocco, et al.. (2006). Simvastatin maintains steady patterns of GFR and improves AER and expression of slit diaphragm proteins in type II diabetes. Kidney International. 70(1). 177–186. 36 indexed citations
19.
Tonks, Ann, David Somerset, Avinash Abhyankar, et al.. (2004). Congenital malformations of the diaphragm: findings of the West Midlands Congenital Anomaly Register 1995 to 2000. Prenatal Diagnosis. 24(8). 596–604. 78 indexed citations
20.
Abhyankar, Avinash, J.J. Corkery, & Anthony Lander. (2001). Postoperative pneumatosis intestinalis in infants does not automatically preclude enteral feeding. Journal of Pediatric Surgery. 36(12). 1820–1823. 2 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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