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Allen N. Lamb | Researchclopedia

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Allen N. Lamb

Decision Sciences (United States)

77

Works

5,419

Citations

35

h-index

51

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Prenatal Screening and Diagnostics Chromosomal and Genetic Variations

Affiliations

Wesleyan University1991–1991

University of North Carolina at Chapel Hill1994–1994

New Mexico Department of Health2007–2007

Madigan Army Medical Center1999–1999

East Carolina University1984–1984

Top Works

Chromosomal Microarray versus Karyotyping for Prenatal Diagnosis

Ronald J. Wapner,Alastair J. Martin,et al.

20121,411 citations

Genetics and Neurodevelopmental Disorders

Genomics and Rare Diseases

Autosomal XX sex reversal caused by duplication ofSOX9

Bing Huang,Shengbiao Wang,et al.

1999425 citations

ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013

Sarah T. South,Charles Lee,et al.

2013374 citations

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome

Angela L. Duker,Blake C. Ballif,et al.

2010317 citations

Whole‐genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray

Justine Coppinger,Sarah Alliman,et al.

2009173 citations

Copy number variations associated with autism spectrum disorders contribute to a spectrum of neurodevelopmental disorders

Jill A. Rosenfeld,Blake C. Ballif,et al.

2010169 citations

High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44

Blake C. Ballif,Jill A. Rosenfeld,et al.

2011146 citations

Chromosomal Microarray Versus Karyotyping for Prenatal Diagnosis

Ronald J. Wapner,Christa Lese Martin,et al.

2013134 citations

Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis

A. Estop,S. Munné,et al.

1998130 citations