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Clelia Negrini, M.D., Ph.D.

Contact Information

Phone Numbers

Office: (585) 275-4912

Fax: (585) 276-2144

Locations

Credentials

Specialties

  • Clinical Genetics (M.D.)
  • Internal Medicine - American Board of Internal Medicine

Education

1990
MD | Arg-Natl Univ of Cordoba
Medicine

Post-doctoral Training & Residency

07/01/1998 - 06/30/1999
Internship in Internal Medicine at Good Samaritan Hospital of Maryland

07/01/1999 - 06/30/2000
Residency in Internal Medicine at Good Samaritan Hospital of Maryland

01/01/2001 - 06/30/2003
Fellowship in Medical Genetics at National Institute of Health

07/01/2003 - 06/30/2004
Residency in Internal Medicine at George Washington University Hospital

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Awards

1991 - 1996
Fogarty Visiting Fellowship National Institutes of Health

1983 - 1984
American Field Service, International Exchange Programs for High School Students Albuquerque Academy, Albuquerque NM


1997 National University of Cordoba, School of Medicine Award for best Ph.D. Thesis.     1991-1996 Fogarty Visiting Fellowship. National Institutes of Health.     1983-1984   American Field Service, International Exchange Programs for High School Students. Albuquerque Academy, Albuquerque NM. High School Diploma.  

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Publications

Journal Articles

4/1998
Liang Y, Wang A, Probst FJ, Arhya IN, Barber TD, Chen KS, Deshmukh D, Dolan DF, Hinnant JT, Carter LE, Jain PK, Lalwani AK, Li XC, Lupski JR, Moeljopawiro S, Morell R, Negrini C, Wilcox ER, Winata S, Camper SA, Friedman TB. "Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2." American journal of human genetics.. 1998 Apr 0; 62(4):904-15.

8/1997
Kalinec F, Kalinec G, Negrini C, Kachar B. "Immunolocalization of anion exchanger 2alpha in auditory sensory hair cells." Hearing research.. 1997 Aug 0; 110(1-2):141-6.

6/1996
O'Neill ME, Marietta J, Nishimura D, Wayne S, Van Camp G, Van Laer L, Negrini C, Wilcox ER, Chen A, Fukushima K, Ni L, Sheffield VC, Smith RJ. "A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6." Human molecular genetics.. 1996 Jun 0; 5(6):853-6.

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