Arti Pandya

5.0k citations

75 papers · 2.7k indexed · h-index 28

Co-authors: Kathleen S. Arnos Walter E. Nance Mustafa Tekin Susan H. Blanton Katherine O. Welch Virginia W. Norris Xia Xia Nathaniel H. Robin
Topics: Hearing, Cochlea, Tinnitus, Genetics (32 papers)Connexins and lens biology (16 papers)Hearing Loss and Rehabilitation (16 papers)
Cited by: Sensory Systems Otorhinolaryngology Neurology
Journals: The Lancet Journal of Biological ChemistrySHILAP Revista de lepidopterología
Partner nations: United States Türkiye Japan

In The Last Decade

Arti Pandya

70 papers receiving 2.6k citations

Peers

Countries citing papers authored by Arti Pandya

Since Specialization

Citations

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

Fields of papers citing papers by Arti Pandya

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arti Pandya

This figure shows the co-authorship network connecting the top 25 collaborators of Arti Pandya. A scholar is included among the top collaborators of Arti Pandya 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 Arti Pandya. Arti Pandya 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	Repurposing of antiangiogenic agents for treatment of vascular anomalies 2023 ·Pharmacology & Therapeutics ·Julie Blatt,(unknown),(unknown),(unknown),Arti Pandya	1
2	Clinical evaluation and etiologic diagnosis of hearing loss: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) 2022 ·Genetics in Medicine ·Marilyn M. Li,Ahmad Abou Tayoun,Marina T. DiStefano,Arti Pandya,Heidi L. Rehm,Nathaniel H. Robin,Amanda M. Schaefer,Christine Yoshinaga‐Itano	37
3	Cancer Risk in Klippel–Trenaunay Syndrome 2019 ·Lymphatic Research and Biology ·Julie Blatt,(unknown),Victoria Price,Shelley E. Crary,Arti Pandya,Denise M. Adams	17
4	Co‐occurring Down syndrome and SUCLA2‐related mitochondrial depletion syndrome 2017 ·American Journal of Medical Genetics Part A ·(unknown),Daniel S. Marchuk,Laurie D. Smith,Alexandra Arreola,Kathleen Kaiser‐Rogers,Joseph Muenzer,Arti Pandya,Müge Güçsavaş‐Çalıkoğlu,Cynthia M. Powell	0
5	Risk Factors Associated With Unilateral Hearing Loss 2013 ·JAMA Otolaryngology–Head & Neck Surgery ·(unknown),Laura M. Dominguez,Derek A. Chapman,Shuhui Wang,Arti Pandya,Kelley M. Dodson	19
6	Performance Evaluation of Two Methods Using Commercially Available Reagents for PCR-Based Detection of FMR1 Mutation 2012 ·Journal of Molecular Diagnostics ·(unknown),Paula Anderson,(unknown),David S. Wilkinson,Arti Pandya,Andrea Ferreira‐Gonzalez	14
7	Etiology of unilateral hearing loss in a national hereditary deafness repository 2012 ·American Journal of Otolaryngology ·Kelley M. Dodson,(unknown),(unknown),Bich Hong Nguyen,Aristides Sismanis,Kathleen S. Arnos,Virginia W. Norris,Derek A. Chapman,Walter E. Nance,Arti Pandya	34
8	Identification of p.A684V missense mutation in the WFS1 gene as a frequent cause of autosomal dominant optic atrophy and hearing impairment 2011 ·American Journal of Medical Genetics Part A ·Nanna Dahl Rendtorff,Marianne Lodahl,Houda Boulahbel,(unknown),Arti Pandya,Katherine O. Welch,Virginia W. Norris,Kathleen S. Arnos,Maria Bitner‐Glindzicz,Sarah B. Emery,Marilyn B. Mets,Toril Fagerheim,Kristina Eriksson,Lars Hestbjerg Hansen,Helene Bruhn,Claes Möller,(unknown),(unknown),Marci M. Lesperance,Lisbeth Tranebjærg	89
9	A Comparative Analysis of the Genetic Epidemiology of Deafness in the United States in Two Sets of Pedigrees Collected More than a Century Apart 2008 ·The American Journal of Human Genetics ·Kathleen S. Arnos,Katherine O. Welch,Mustafa Tekin,Virginia W. Norris,Susan H. Blanton,Arti Pandya,Walter E. Nance	30
10	Compound heterozygosity for dominant and recessive GJB2 mutations: Effect on phenotype and review of the literature 2007 ·American Journal of Medical Genetics Part A ·Katherine O. Welch,(unknown),Arti Pandya,Kathleen S. Arnos	31
11	A focus group study of consumer attitudes toward genetic testing and newborn screening for deafness 2006 ·Genetics in Medicine ·(unknown),(unknown),Kathleen S. Arnos,Andrea L. Kalfoglou,Arti Pandya	34
12	Chudley‐McCullough syndrome: Expanded phenotype and review of the literature 2003 ·American Journal of Medical Genetics Part A ·Katherine O. Welch,Mustafa Tekin,Walter E. Nance,Susan H. Blanton,Kathleen S. Arnos,Arti Pandya	11
13	Type I Collagen Triplet Duplication Mutation in Lethal Osteogenesis Imperfecta Shifts Register of α Chains throughout the Helix and Disrupts Incorporation of Mutant Helices into Fibrils and Extracellular Matrix 2003 ·Journal of Biological Chemistry ·Wayne A. Cabral,(unknown),Elena Makareeva,Alain Colige,Mustafa Tekin,Arti Pandya,Sergey Leikin,Joan C. Marini	27
14	Advances in hereditary deafness 2001 ·The Lancet ·Mustafa Tekin,Kathleen S. Arnos,Arti Pandya	121
15	W44C mutation in the connexin 26 gene associated with dominant non‐syndromic deafness 2001 ·Clinical Genetics ·Mustafa Tekin,(unknown),X.-J. Xia,(unknown),Liu Xz,Nance We,Arti Pandya	18
16	Two Genes That Map to the STSL Locus Cause Sitosterolemia: Genomic Structure and Spectrum of Mutations Involving Sterolin-1 and Sterolin-2, Encoded by ABCG5 and ABCG8, Respectively 2001 ·The American Journal of Human Genetics ·Kangmo Lu,(unknown),E. Starr Hazard,Angela Brooks‐Wilson,Hideki Hidaka,Hideto Kojima,Leiv Ose,Anton F. H. Stalenhoef,(unknown),Ingemar Björkhem,Eric Bruckert,Arti Pandya,H. Bryan Brewer,Gerald Salen,Michael Dean,Anand K. Srivastava,Shailendra B. Patel	282
17	Discordant retinoblastoma in monozygotic twins 1999 ·American Journal of Ophthalmology ·Dennis M. Marcus,(unknown),(unknown),Arti Pandya,Steven E. Brooks	5
18	Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: Growth, development, and profiles 1999 ·American Journal of Medical Genetics ·Gene S. Fisch,Nancy J. Carpenter,Jeanette J. A. Holden,Richard J. Simensen,Patricia N. Howard‐Peebles,Anne Maddalena,Arti Pandya,Walter E. Nance	36
19	Implications of Molecular Diagnostic Testing in Families with Hereditary Pancreatitis 1997 ·Genetic Testing ·Arti Pandya,X.-J. Xia,Susan H. Blanton,(unknown),Thomas C. Markello,W E Nance	4
20	Interstitial deletion of the long arm of chromosome 6 associated with unusual limb anomalies: Report of two new patients and review of the literature 1995 ·American Journal of Medical Genetics ·Arti Pandya,Nancy Braverman,Reed E. Pyeritz,(unknown),Antonie D. Kline,Rena E. Falk	21

About Arti Pandya

Arti Pandya is a scholar working on Sensory Systems, Developmental Biology and Neurology, having authored 75 papers that have together received 2.7k indexed citations. Recurring topics across this work include Hearing, Cochlea, Tinnitus, Genetics (32 papers), Connexins and lens biology (16 papers) and Hearing Loss and Rehabilitation (16 papers). The work is most often cited by research in Sensory Systems (1.3k citations), Otorhinolaryngology (291 citations) and Neurology (403 citations). Arti Pandya has collaborated with scholars based in United States, Türkiye and Japan. Frequent co-authors include Kathleen S. Arnos, Walter E. Nance, Mustafa Tekin, Susan H. Blanton, Katherine O. Welch, Virginia W. Norris, Xia Xia, Nathaniel H. Robin, Heidi L. Rehm and Christine Yoshinaga‐Itano. Their work appears in journals such as The Lancet, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

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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