Avinash Abhyankar

7.4k citations

30 papers · 1.9k indexed · h-index 20

Co-authors: Jean‐Laurent Casanova Laurent Abel Arnold Münnich Patrick Nitschké Agata Smogorzewska Arleen D. Auerbach Francis P. Lach Emmanuelle Jouanguy
Topics: Genomics and Rare Diseases (10 papers)Immunodeficiency and Autoimmune Disorders (5 papers)Genetics and Neurodevelopmental Disorders (5 papers)
Cited by: Genetics Immunology Aging
Journals: Proceedings of the National Academy of Sciences Journal of Clinical Investigation Nature Genetics
Partner nations: United States France United Kingdom

In The Last Decade

Avinash Abhyankar

30 papers receiving 1.9k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease 2023 ·Circulation Genomic and Precision Medicine ·Thomas Hays,Rebecca Hernan,(unknown),(unknown),(unknown),(unknown),Ganga Krishnamurthy,(unknown),Atteeq U. Rehman,Amanda Thomas‐Wilson,Saurav Guha,(unknown),Volkan Okur,(unknown),Vanessa Felice,Avinash Abhyankar,Vaidehi Jobanputra,Wendy K. Chung	11
2	Embryonic lethal genetic variants and chromosomally normal pregnancy loss 2021 ·Fertility and Sterility ·Jennie Kline,Badri N. Vardarajan,Avinash Abhyankar,(unknown),Bruce Levin,Nara Sobreira,Andrew Tang,Amanda Thomas‐Wilson,(unknown),Vaidehi Jobanputra	8
3	Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies 2020 ·Journal of Molecular Diagnostics ·Vaidehi Jobanputra,Peter Andrews,Vanessa Felice,Avinash Abhyankar,(unknown),(unknown),(unknown),Inessa Hakker,Kazimierz O. Wrzeszczyński,Michael Ronemus	1
4	Distinct roles of BRCA2 in replication fork protection in response to hydroxyurea and DNA interstrand cross-links 2020 ·Genes & Development ·Kimberly A. Rickman,(unknown),Francis P. Lach,Sunandini Sridhar,Anderson T. Wang,Avinash Abhyankar,Athena L. Huang,Michael C. Kelly,Arleen D. Auerbach,Agata Smogorzewska	50
5	Prenatal Diagnosis by Whole Exome Sequencing in Fetuses with Ultrasound Abnormalities 2018 ·Methods in molecular biology ·Vanessa Felice,Avinash Abhyankar,Vaidehi Jobanputra	3
6	Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency 2017 ·Clinical Case Reports ·Avinash Abhyankar,Michelle F. Lamendola-Essel,Kelly Brennan,Jessica L. Giordano,Cecilia Esteves,Vanessa Felice,Ronald J. Wapner,Vaidehi Jobanputra	13
7	Differential burden of rare protein truncating variants in Alzheimer’s disease patients compared to centenarians 2016 ·Human Molecular Genetics ·Yun Freudenberg‐Hua,Wentian Li,Avinash Abhyankar,Vladimir Vacic,(unknown),Danny Ben‐Avraham,Jeremy Koppel,Blaine Greenwald,Søren Germer,Robert B. Darnell,Nir Barzilai,Jan Freudenberg,Gil Atzmon,Peter Davies	8
8	Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia 2015 ·Cell Reports ·Kimberly A. Rickman,Francis P. Lach,Avinash Abhyankar,Frank X. Donovan,Erica Sanborn,Jennifer A. Kennedy,Carrie Sougnez,Stacey Gabriel,Olivier Elemento,Settara C. Chandrasekharappa,Detlev Schindler,Arleen D. Auerbach,Agata Smogorzewska	111
9	A Novel Homozygous p.R1105X Mutation of the AP4E1 Gene in Twins with Hereditary Spastic Paraplegia and Mycobacterial Disease 2013 ·PLoS ONE ·Xiao‐Fei Kong,Aziz Bousfiha,(unknown),Yuval Itan,Avinash Abhyankar,Vanessa L. Bryant,Satoshi Okada,Fatima Ailal,Jacinta Bustamante,Jean‐Laurent Casanova,Jennifer Hirst,Stéphanie Boisson‐Dupuis	27
10	The human gene connectome as a map of short cuts for morbid allele discovery 2013 ·Proceedings of the National Academy of Sciences ·Yuval Itan,Shen‐Ying Zhang,Guillaume Vogt,Avinash Abhyankar,Melina Herman,Patrick Nitschké,Dror Fried,Lluís Quintana‐Murci,Laurent Abel,Jean‐Laurent Casanova	46
11	A Mild Form of SLC29A3 Disorder: A Frameshift Deletion Leads to the Paradoxical Translation of an Otherwise Noncoding mRNA Splice Variant 2012 ·PLoS ONE ·Alexandre Bolze,Avinash Abhyankar,Audrey V. Grant,(unknown),Ruchi Yadav,Minji Byun,(unknown),Jean‐François Emile,Marçal Pastor‐Anglada,Laurent Abel,Anne Puel,Rajgopal Govindarajan,Loïc de Pontual,Jean‐Laurent Casanova	44
12	Exome Sequencing Identifies PDE4D Mutations as Another Cause of Acrodysostosis 2012 ·The American Journal of Human Genetics ·Caroline Michot,Carine Le Goff,Alice Goldenberg,Avinash Abhyankar,Céline Klein,Esther Kinning,Anne‐Marie Guerrot,(unknown),(unknown),Geneviève Baujat,Stanislas Lyonnet,Caroline Thalassinos,Patrick Nitschké,Jean‐Laurent Casanova,Martine Le Merrer,Arnold Münnich,Valérie Cormier‐Daire	84
13	Inherited MST1 Deficiency Underlies Susceptibility to EV-HPV Infections 2012 ·PLoS ONE ·Amandine Créquer,Capucine Pïcard,Étienne Patin,(unknown),Avinash Abhyankar,Martine Münzer,Marianne Debré,Shen‐Ying Zhang,Geneviève de Saint Basile,Alain Fischer,Laurent Abel,Gérard Orth,Jean‐Laurent Casanova,Emmanuelle Jouanguy	92
14	De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy 2012 ·Nature Genetics ·Giulia Barcia,Matthew R. Fleming,(unknown),Valeswara‐Rao Gazula,Maile R. Brown,Maéva Langouët,Haijun Chen,Jack Kronengold,Avinash Abhyankar,(unknown),Patrick Nitschké,Anna Kamińska,Nathalie Boddaert,Jean‐Laurent Casanova,Isabelle Desguerre,Arnold Münnich,Olivier Dulac,Leonard K. Kaczmarek,Laurence Colleaux,Rima Nabbout	335
15	Mutations at a single codon in Mad homology 2 domain of SMAD4 cause Myhre syndrome 2011 ·Nature Genetics ·Carine Le Goff,Clémentine Mahaut,Avinash Abhyankar,Wilfried Le Goff,Valérie Serre,Alexandra Afenjar,Anne Destrèe,Maja Di Rocco,Delphine Héron,Sébastien Jacquemont,Sandrine Marlin,Marleen Simon,John Tolmie,Alain Verloès,Jean‐Laurent Casanova,Arnold Münnich,Valérie Cormier‐Daire	117
16	Whole-Exome-Sequencing-Based Discovery of Human FADD Deficiency 2010 ·The American Journal of Human Genetics ·Alexandre Bolze,Minji Byun,David McDonald,Neil V. Morgan,Avinash Abhyankar,Lakshmanane Premkumar,Anne Puel,Chris M. Bacon,Frédéric Rieux‐Laucat,Ki Pang,(unknown),Laurent Abel,Andrew J. Cant,Eamonn R. Maher,Stefan J. Riedl,Sophie Hambleton,Jean‐Laurent Casanova	118
17	Comparative Sequence Analysis of the Non-Protein-Coding Mitochondrial DNA of Inbred Rat Strains 2009 ·PLoS ONE ·Avinash Abhyankar,Hee-Bok Park,Giancarlo Tonolo,Holger Luthman	15
18	Simvastatin maintains steady patterns of GFR and improves AER and expression of slit diaphragm proteins in type II diabetes 2006 ·Kidney International ·Giancarlo Tonolo,Mario Velussi,Enrico Brocco,Cataldo Abaterusso,Andrea Carraro,Giuseppe Morgia,Andrea Satta,(unknown),Avinash Abhyankar,Holger Luthman,R. Nosadini	36
19	Congenital malformations of the diaphragm: findings of the West Midlands Congenital Anomaly Register 1995 to 2000 2004 ·Prenatal Diagnosis ·Ann Tonks,(unknown),David Somerset,(unknown),Avinash Abhyankar,Indrani C. Bagchi,Anthony Lander,E. Roberts,Mark D. Kilby	78
20	Postoperative pneumatosis intestinalis in infants does not automatically preclude enteral feeding 2001 ·Journal of Pediatric Surgery ·Avinash Abhyankar,J.J. Corkery,Anthony Lander	2

About Avinash Abhyankar

Avinash Abhyankar is a scholar working on Genetics, Nephrology and Immunology, having authored 30 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (10 papers), Immunodeficiency and Autoimmune Disorders (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Genetics (650 citations), Immunology (358 citations) and Aging (27 citations). Avinash Abhyankar has collaborated with scholars based in United States, France and United Kingdom. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature 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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