Erin Carmany, MS, CGC
Associate Program Director of the Genetic Counseling Program


2375 Scott Hall
313-577-9138
ecarmany@med.wayne.edu


 




Research interests

Genetic counseling in the Spanish speaking population, alternative genetic counseling service models
 

Selected publications

 

Muller, E, Aradya S, Atkin J, Carmany E, Elliot A, Chudley A, Clark R, Everman D, Garner S, Hall B, Herman G, Kivuva E, Ramanathan S, Stevenson D, Stockton D, Hudgins L.  Microdeletion 9q22.3 Syndrome Includes Metopic Craniosynostosis, Hydrocephalus, Macrosomia and Developmental Delay.   American Journal of Medical Genetics: Part A . (2012) 158:2, 391-9. 

 

Carmany EP, Bawle EV.  Microduplication of 4p16.3 due to an unbalanced translocation resulting in a mild phenotype.   American Journal of Medical Genetics: Part A.  (2011) 155:4, 819-24.

 

Girirajan S, Rosenfeld J, Coe B, Parikh S, Friedman N, Goldstein A, Filipink R, McConnell J, Angle B, Meschino W, Nezarati M, Asamoah A, Jackson K, Gowans G, Martin J, Carmany E, Stockton D, Schnur R, Penney L, Martin D, Raskin S, Leppig K, Thiese H, Smith R, Aberg E, Niyazov D, Escobar L, El-Khechen D, Johnson K, Lebel R, Siefkas K, Ball S, Shur N, McGuire M, Brasington C, Spence JE, Martin L, Clericuzio C, Ballif B, Shaffer L, Eichler E.  Multiple rare CNVs contribute to the phenotypic heterogeneity of genomic disorders.   New England Journal of Medicine.    12 Sept 2012 [Epub ahead of print] 

 

Kleyn M, Langbo C, Abdulhamd I, Adamski C, Allan C, Carmany E, Gregoire-Bottex M, Homnick D, Schuen J, Nasr S.  Evaluation of Genetic Counseling among Cystic Fibrosis Carriers, Michigan Newborn Screening.   Pediatric Pulmonology .  In Press. 





 
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