SigridWayneMD

Pathology • Tulsa, OK

Anatomic Pathology, Clinical Pathology

Physician

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Office
6161 S Yale Ave
Tulsa, OK 74136
Phone+1 918-742-1478
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Education & Training

UPMC Medical Education (Presbyterian Shadyside Hospital) AFellowship, Selective Pathology, 2007 - 2008
University of Iowa Hospitals and ClinicsResidency, Pathology-Anatomic and Clinical, 2002 - 2006
University of Iowa Hospitals and ClinicsInternship, Transitional Year, 1997 - 1998
University of Iowa Roy J. and Lucille A. Carver College of MedicineClass of 1997

Certifications & Licensure

OK State Medical License 2008 - 2025
PA State Medical License 2005 - 2008
IA State Medical License 1997 - 2007
American Board of Pathology Pathology - Anatomic/Pathology - Clinical

Publications & Presentations

PubMed

7 citations
AP-2 participates in the transcriptional control of the amyloid precursor protein (APP) gene in oral squamous cell carcinoma
Matthew J. Provenzano, Lei Yu, Michael J. Hitchler, Matthew P. Fitzgerald, Robert A. Robinson, Sigrid Wayne, Mark R. Ver Meer, Frederick E. Domann> ;Experimental and Molecular Pathology. 2007 Oct 1
9 citations
Upper aerodigestive tract squamous dysplasia: correlation with p16, p53, pRb, and Ki-67 expression.
Sigrid Wayne, Robert A. Robinson> ;Archives of Pathology & Laboratory Medicine. 2006 Sep 1
10 citations
DFNA10/EYA4--the clinical picture.
E.M.R. De Leenheer, Patrick L. M. Huygen, Sigrid Wayne, M. Verstreken, Frank Declau, G. Van Camp, P. Van de Heyning, Richard J.H. Smith, C.W.R.J. Cremers> ;Advances in Oto-Rhino-Laryngology. 2002 Jan 1
224 citations
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
Kumar N. Alagramam, Huijun Yuan, Markus H. Kuehn, Crystal L. Murcia, Sigrid Wayne, C. R. Srikumari Srisailpathy, R. Brian Lowry, Russell Knaus, Lut Van Laer, Francois ...> ;Human Molecular Genetics. 2001 Aug 1
155 citations
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus
Sigrid Wayne, Nahid G. Robertson, Frank DeClau, Nancy Chen, Kristien Verhoeven, Sai Prasad, Lisbeth Tranebjärg, Cynthia C. Morton, Allen F. Ryan, Guy Van Camp, Richard...> ;Human Molecular Genetics. 2001 Feb 1
411 citations
Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23
Julie M. Bork, Linda M. Peters, Saima Riazuddin, S. L. Bernstein, Zubair M. Ahmed, Seth L. Ness, Robert C. Polomeno, Arabandi Ramesh, Melvin D. Schloss, C. R. Srikumar...> ;American Journal of Human Genetics. 2001 Jan 1
9 citations
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.
Kristien Verhoeven, Toril Fagerheim, Sai Prasad, Sigrid Wayne, Frank De Clau, Wendy Balemans, M. Verstreken, Isabelle Schatteman, Bjorn Solem, Paul Van de Heyning, Lis...> ;Human Genetics. 2000 Jul 1
32 citations
Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.
John H. Greinwald, Sigrid Wayne, Achih H. Chen, Daryl A. Scott, Ross I. S. Zbar, M. L. Kraft, Sai Prasad, Arabandi Ramesh, Paul Coucke, C. R. Srikumari Srisailapathy, ...> ;American Journal of Medical Genetics. 1998 Jun 30
17 citations
Passage to India: The Search for Genes Causing Autosomal Recessive Nonsyndromic Hearing Loss:
Ross I. S. Zbar, Arabandi Ramesh, C. R. Srikumari Srisailapathy, Kunihiro Fukushima, Sigrid Wayne, Richard J.H. Smith> ;Otolaryngology--Head and Neck Surgery. 1998 Mar 1
40 citations
New gene for autosomal recessive non‐syndromic hearing loss maps to either chromosome 3q or 19p
Achih Chen, Sigrid Wayne, Adam M. Bell, Arabandi Ramesh, C. R. Srikumari Srisailapathy, Daryl A. Scott, Val C. Sheffield, Peter Van Hauwe, Ross I. S. Zbar, Jennifer As...> ;American Journal of Medical Genetics. 1997 Sep 5
92 citations
Localization of the Usher Syndrome Type ID Gene (Ush1D) to Chromosome 10
Sigrid Wayne, Vazken M. Der Kaloustian, Melvin D. Schloss, Robert C. Polomeno, Daryl A. Scott, J. Fielding Hejtmancik, Val C. Sheffield, Richard J.H. Smith> ;Human Molecular Genetics. 1996 Oct 1
48 citations
A Gene for Autosomal Dominant Late-Onset Progressive Non-Syndromic Hearing Loss, DFNA10, Maps to Chromosome 6
Marsha E. O'Neill, Jacquie Marietta, Darryl Y. Nishimura, Sigrid Wayne, Guy Van Camp, Lut Van Laer, Clelia Negrini, Edward R. Wilcox, Achih Chen, Kunihiro Fukushima, L...> ;Human Molecular Genetics. 1996 Jun 1
55 citations
A human recessive neurosensory nonsyndromic hearing impairment locus is a potential homologue of the murine deafness (dn) locus
Pawan K. Jain, Kunihiro Fukushima, Dilip Deshmukh, Arabandi Ramesh, Elizabeth A. Thomas, Anil K. Lalwani, Subrinder Kumar, Barbara Ploplis, Hana Skarka, C. R. Srikumar...> ;Human Molecular Genetics. 1995 Dec 1
40 citations
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.
Kunihiro Fukushima, Arabandi Ramesh, C. R.S. Srisailapathy, Li Ni, Sigrid Wayne, Michelle O'Neill, G. Van Camp, P. Coucke, P. Jain, E. R. Wilcox, Shelley D. Smith, Jud...> ;Genome Research. 1995 Oct 1
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Hospital Affiliations

Saint Francis HospitalTulsa, Oklahoma
PAM Health Specialty Hospital of TulsaTulsa, Oklahoma
Jack C. Montgomery Department of Veterans Affairs Medical CenterMuskogee, Oklahoma

SigridWayneMD

Dr. Wayne is on Doximity

Education & Training

Certifications & Licensure

Publications & Presentations

Hospital Affiliations

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