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RH

R. Scott Hansen

Independent Researcher

114
Publications
26,182
Citations
40
H-Index
55
i10-Index
0
2yr Mean Cite
-
Cite/Paper
Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

0 total

Global increases in both common and rare copy number load associated with autism OA

S. Girirajan, Rebecca Lynn Johnson, F. Tassone, J. Balciuniene, N. Katiyar - Human Molecular Genetics, 2013
Cited by 59 Semantic Scholar

Identifying patterns of copy number variants in case-control studies of human genetic disorders

A. Alqallaf, A. Tewfik, P. Krakowiak, F. Tassone, R. Davis - 2009 IEEE International Workshop on Genomic Signal Processing and Statistics, 2009
Cited by 3 Semantic Scholar

An antisense transcript spanning the CGG repeat region of FMR1 is upregulated in premutation carriers but silenced in full mutation individuals. OA

P. Ladd, L. E. Smith, N. Rabaia, James M. Moore, S. A. Georges - Human Molecular Genetics, 2007
Cited by 265 Semantic Scholar

Research Topics

Epigenetics and DNA Methylation (28) Genetics and Neurodevelopmental Disorders (24) Genomics and Chromatin Dynamics (16) RNA modifications and cancer (14) Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8)

Affiliations

National Institutes of Health
US 1999 - 1999
City Of Hope National Medical Center
US 1990 - 1990
University of Denver
US 2003 - 2003
Harvard University
US 2003 - 2003
University of Washington
US 2015 - 1970

External Profiles

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