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SR

Sally Rosengren

Medical Genetics / Clinical Genetics (M.D.)

Credentials: ·

History

Pediatrics

Research

Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities
Nature Genetics · 2008 · 459 citations
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss
Human Mutation · 1998 · 206 citations
Transcriptional control of SLC26A4 is involved in Pendred syndrome and nonsyndromic enlargement of vestibular aqueduct (DFNB4)
The American Journal of Human Genetics · 2007 · 164 citations

Elizabeth Roeder
3 papers
James Lupski
2 papers
JH
Jeffrey Hyams
2 papers
JR
John Rodis
2 papers
Mary-Alice Abbott
2 papers
Richard Smith
2 papers
AZ
Aaron Zucker
1 paper
AG
Adolfo Garnica
1 paper
Alexander Paciorkowski
1 paper · 1 as a resident
AV
Anthony Vintzileos
1 paper
BN
Beata Nowakowska
1 paper
Brendan Lee
1 paper