Concepedia

Stacy E. Harris

SE

Statistics

Publications

4

Citations

424

H-Index

4

Active since

2003

Affiliations

Children's Hospital of Philadelphia(Current)

University of Pennsylvania

Stacy E. Harris is an author at Children's Hospital of Philadelphia specializing in molecular genetics, digeorge syndrome, and genetics.

Publications per year

2003–2005

4

Publications

4

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion

Sulagna C. Saitta, Stacy E. Harris, Ann P. Gaeth et al. · Human Molecular Genetics · 2003 · 147 citations · Full text

, , +17

Effects of a Functional COMT Polymorphism on Prefrontal Cognitive Function in Patients With 22q11.2 Deletion Syndrome

Carrie E. Bearden, Abbas F. Jawad, David R. Lynch et al. · American Journal of Psychiatry · 2004 · 132 citations

, , +17

Independent de novo 22q11.2 deletions in first cousins with DiGeorge/velocardiofacial syndrome

Sulagna C. Saitta, Stacy E. Harris, Donna M. McDonald‐McGinn et al. · American Journal of Medical Genetics Part A · 2003 · 103 citations · Full text

, , +14

Effects of Comt Genotype on Behavioral Symptomatology in the 22q11.2 Deletion Syndrome

Carrie E. Bearden, Abbas F. Jawad, David R. Lynch et al. · Child Neuropsychology · 2005 · 42 citations

, , +17

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