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Genetics

D-Index
60
Citations
12923
World Ranking
3156
National Ranking
1377

Overview

Nathan Fischel-Ghodsian is affiliated with the University of California, Los Angeles in the United States. Their academic profile currently reflects involvement in research activities based at this institution.

No recent papers, frequent publication venues, co-authors, or awards are listed for Nathan Fischel-Ghodsian. There is also no available information on their specific fields of study, subfields, or main topics of work from the data provided.

The absence of listed publications or detailed research topics suggests that publicly available records or database entries for Nathan Fischel-Ghodsian are limited. This profile, therefore, reflects only confirmed affiliations without additional bibliometric or scholarly contributions documented at this time.

Best Publications

  • Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.

    T R Prezant;J V Agapian;M C Bohlman;X Bu

  • Recombination at the human α-globin gene cluster: Sequence features and topological constraints

    R.D. Nicholls;N. Fischel-Ghodsian;D.R. Higgs

  • A molecular basis for human hypersensitivity to aminoglycoside antibiotics.

    Tim Hutchin;Ian Haworth;Koichiro Higashi;Nathan Fischel-Ghodsian

  • Missense Mutation in Pseudouridine Synthase 1 (PUS1) Causes Mitochondrial Myopathy and Sideroblastic Anemia (MLASA)

    Yelena Bykhovskaya;Kari Casas;Emebet Mengesha;Aida Inbal

  • Genetic factors in aminoglycoside toxicity.

    Nathan Fischel-Ghodsian

  • A genome-wide search identifies potential new susceptibility loci for Crohn's disease

    Yuanhong Ma;Jeffrey D. Ohmen;Zhiming Li;L. Gordon Bentley

  • Biochemical Evidence for Nuclear Gene Involvement in Phenotype of Non-Syndromic Deafness Associated with Mitochondrial 12S rRNA Mutation

    Min-Xin Guan;Nathan Fischel-Ghodsian;Giuseppe Attardi

  • Mitochondrial deafness mutations reviewed.

    Nathan Fischel-Ghodsian

  • Phenotype-genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis.

    M Shohat;N Magal;T Shohat;X Chen

  • Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutations

    Min-Xin Guan;Min-Xin Guan;Qingfeng Yan;Xiaoming Li;Yelena Bykhovskaya

  • A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

    Min-Xin Guan;Nathan Fischel-Ghodsian;Giuseppe Attardi

  • Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

    Min-Xin Guan;Nathan Fischel-Ghodsian;Giuseppe Attardi

  • Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNASer(UCN) gene

    C.M. Sue;K. Tanji;G. Hadjigeorgiou;A.L. Andreu

  • Susceptibility Locus for Inflammatory Bowel Disease on Chromosome 16 has a Role in Crohn's disease, but Not in Ulcerative Colitis

    Jeffrey D. Ohmen;Hui-Ying Yang;Karen K. Yamamoto;Hong-Yu Zhao

  • Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity

    Nathan Fischel-Ghodsian;Toni R. Prezant;Xiangdong Bu;Sitki Öztas

  • Mitochondrial gene mutation is a significant predisposing factor in aminoglycoside ototoxicity

    Nathan Fischel-Ghodsian;Nathan Fischel-Ghodsian;Nathan Fischel-Ghodsian;Toni R. Prezant;Toni R. Prezant;Toni R. Prezant;William E. Chaltraw;William E. Chaltraw;William E. Chaltraw;Kimberly A. Wendt;Kimberly A. Wendt;Kimberly A. Wendt

  • Stable length polymorphism of up to 260 kb at the tip of the short arm of human chromosome 16.

    Andrew O.M. Wilkie;Douglas R. Higgs;Katrina A. Rack;Veronica J. Buckle

  • Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafness.

    Kevin B. Sevior;Atsushi Hatamochi;Ian A. Stewart;Yelena Bykhovskaya

  • Age-related hearing loss and the ahl locus in mice.

    Elizabeth M. Keithley;Cecilia Canto;Qing Yin Zheng;Nathan Fischel-Ghodsian

  • Inherited susceptibility to aminoglycoside ototoxicity: genetic heterogeneity and clinical implications.

    Rosaria A.M.S. Casano;David F. Johnson;Yelena Bykhovskaya;Francesca Torricelli

Frequent Co-Authors

Jerome I. Rotter
Jerome I. Rotter UCLA Medical Center
Mordechai Shohat
Mordechai Shohat Tel Aviv University
Min-Xin Guan
Min-Xin Guan Zhejiang University
Kent D. Taylor
Kent D. Taylor David Geffen School of Medicine at UCLA
Stephan R. Targan
Stephan R. Targan Cedars-Sinai Medical Center
Michael Centola
Michael Centola Haus Bioceuticals
Daniel L. Kastner
Daniel L. Kastner National Institutes of Health
Robert I. Richards
Robert I. Richards University of Adelaide
John M. Graham
John M. Graham Cedars-Sinai Medical Center

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