ArthurBZinnMD

Medical Genetics • Cleveland, OH

Clinical Biochemical Genetics, Clinical Genetics

Associate Professor, Genetics, Case Western Reserve University School of Medicine

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Office
11100 Euclid Ave
Cleveland, OH 44106
Phone+1 216-844-3936

Fax+1 216-286-6341
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Summary

Dr. Arthur Zinn, MD is a board certified medical geneticist in Cleveland, Ohio. He is currently licensed to practice medicine in Ohio. He is affiliated with University Hospitals Cleveland Medical Center and is an Associate Professor at Case Western Reserve University School of Medicine.

Education & Training

University of MinnesotaResidency, Pediatrics, 1977 - 1979
Case Western Reserve University School of MedicineClass of 1976

Certifications & Licensure

OH State Medical License 1982 - 2023
American Board of Medical Genetics and Genomics Clinical Genetics

Awards, Honors, & Recognition

Regional Top Doctor Castle Connolly, 2014

Publications & Presentations

PubMed

7 citations
Achalasia as the harbinger of a novel mitochondrial disorder in childhood.
Sara Shanske, Michio Hirano, Arthur B Zinn, Mark Cohen, Kevin McNeeley, Thomas C. Chelimsky, Gisela Chelimsky> ;Journal of Pediatric Gastroenterology and Nutrition. 2005 Apr 1
18 citations
Maternal uniparental disomy chromosome 14: case report and literature review.
Marni J. Falk, Christine A. Curtis, Nancy Bass, Arthur B. Zinn, Stuart Schwartz> ;Pediatric Neurology. 2005 Feb 1
12 citations
A 13-year-old boy with cognitive impairment, retinoblastoma, and Wilson disease.
David E. Riley, Max Wiznitzer, Stuart Schwartz, Arthur B. Zinn> ;Neurology. 2001 Jul 10
1 citations
Maculopathy in spinocerebellar ataxia type 7
M. J. Morrow, Arthur B. Zinn, Tarvez Tucker, Richard Leigh> ;Neurology. 1999 Jul 1
13 citations
Pendular nystagmus in patients with peroxisomal assembly disorder
Adriana A. Kori, Nathaniel H. Robin, Jonathan B. Jacobs, Daniel M. Erchul, Osama O. Zaidat, Bernd F. Remler, Lea Averbuch-Heller, Louis F. Dell'Osso, R. John Leigh, Ar...> ;Archives of Neurology. 1998 Apr 1
45 citations
Recurrent immune cytopenias in two patients with DiGeorge/velocardiofacial syndrome.
Andrew D. DePiero, Eli M. Lourie, Brian W. Berman, Nathaniel H. Robin, Arthur B. Zinn, Robert Hostoffer> ;The Journal of Pediatrics. 1997 Sep 1
140 citations
Characterization of Neo-Centromeres in Marker Chromosomes Lacking Detectable Alpha-satellite DNA
Theresa W. Depinet, Joleen L. Zackowski, William C. Earnshaw, Sara Kaffe, Gurbax S. Sekhon, Richard Stallard, Beth A. Sullivan, Gail H. Vance, Daniel L. Van Dyke, Hunt...> ;Human Molecular Genetics. 1997 Aug 1
25 citations
Sex Chromosome Markers: Characterization Using Fluorescence in Situ Hybridization and Review of the Literature
Stuart Schwartz, Theresa W. Depinet, Julie Leana-Cox, Nelson B. Isada, Evelyn M. Karson, Vicki M. Park, Linda M. Pasztor, Linda C. Sheppard, Richard Stallard, Daynna J...> ;American Journal of Medical Genetics. 1997 Jul 11
141 citations
The clinical introduction of genetic testing for Alzheimer disease: An ethical perspective
Stephen G. Post, Peter J. Whitehouse, Robert H. Binstock, Thomas D. Bird, Sharen K. Eckert, Lindsay A. Farrer, Leonard M. Fleck, Atwood D. Gaines, Eric T. Juengst, Har...> ;JAMA. 1997 Mar 12
108 citations
Delineation of the Marfan phenotype associated with mutations in exons 23-32 of the FBN1 gene.
Elizabeth A. Putnam, Mimi Cho, Arthur B. Zinn, Jeffrey A. Towbin, Peter H. Byers, Dianna M. Milewicz> ;American Journal of Medical Genetics. 1996 Mar 29
28 citations
The need for anonymous genetic counseling and testing
Maxwell J. Mehlman, Eric Kodish, Peter J. Whitehouse, Arthur B. Zinn, Sharmon Sollitto, Joshua Berger, Emmeline J. Chiao, Melissa S. Dosick, Suzanne B. Cassidy> ;American Journal of Human Genetics. 1996 Feb 1
88 citations
Inherited WT1 mutation in Denys-Drash syndrome.
Max J. Coppes, Gerrit Jan Liefers, M Higuchi, A B Zinn, J W Balfe, Bryan R.G. Williams> ;Cancer Research. 1992 Nov 1
24 citations
Ethylmalonic/adipic aciduria: effects of oral medium-chain triglycerides, carnitine, and glycine on urinary excretion of organic acids, acylcarnitines, and acylglycines.
Piero Rinaldo, Roy D. Welch, Stephen F. Previs, Eberhard Schmidt-Sommerfeld, J. Jay Gargus, John J. O'Shea, Arthur B. Zinn> ;Pediatric Research. 1991 Sep 1
8 citations
Enamel defects: a developmental marker for hemifacial microsomia.
David C. Johnsen, Barbara M. Weissman, Gail S. Murray, Arthur B. Zinn> ;American Journal of Medical Genetics. 1990 Aug 1
29 citations
Distal deletion of the short arm of chromosome 6.
Vickie L. Zurcher, Wendy L. Golden, Arthur B. Zinn> ;American Journal of Medical Genetics. 1990 Feb 1
17 citations
Molecular analysis of 46,XY females and regional assignment of a new Y-chromosome-specific probe.
Michael A. Cantrell, James N. Bicknell, Roberta A. Pagon, David C. Page, David C. Walker, Howard M. Saal, Arthur B. Zinn, Christine M. Disteche> ;Human Genetics. 1989 Aug 1
51 citations
Psychological response to amniocentesis: II. Effects of coping style.
Sean Phipps, Arthur B. Zinn, John M. Opitz, James F. Reynolds> ;American Journal of Medical Genetics. 1986 Sep 1
26 citations
Psychological response to amniocentesis: I. Mood state and adaptation to pregnancy.
Sean Phipps, Arthur B. Zinn, John M. Opitz, James F. Reynolds> ;American Journal of Medical Genetics. 1986 Sep 1
Characterization of a familial balanced rec(13) in a child with mild MR and his half-sibling with two structurally rearranged chromosomes 13.
Mehra, S., Christ, L., Jeng, L., Zinn, A. B., Schwartz, S.> ;Am J Med Genet A. 2005 Aug 30
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Hospital Affiliations

University Hospitals Cleveland Medical CenterCleveland, Ohio