Author

Wendy L. Golden

Observed names: W Golden, W L Golden, W. Golden, W. L. Golden, W.L. Golden, Wendy Golden, Wendy L Golden

Observed institutions: Roswell Park Comprehensive Cancer Center, University of Pittsburgh, University of Oslo, University of Virginia Health System, Yale University, Children's Hospital of Pittsburgh, University of Virginia Medical Center, University of Virginia Cancer Center, University of Virginia, Case Western Reserve University, Virginia Commonwealth University Medical Center

OpenAlex ID: A5077543909

Genomic instability and catalase gene amplification induced by chronic exposure to oxidative stress.

1998 · C R Hunt, J E Sim, et al. · PubMed · 151

A Chimeric RNA Characteristic of Rhabdomyosarcoma in Normal Myogenesis Process

2013 · Huiling Yuan, Fujun Qin, et al. · Cancer Discovery · 84

Genetic and phenotypic changes associated with the acquisition of tumorigenicity in human bladder cancer

2000 · John J. Gildea, Wendy L. Golden, et al. · Genes Chromosomes and Cancer · 80

Development and characterization of xenograft model systems for adenoid cystic carcinoma

2011 · Christopher A Moskaluk, Alexander S Baras, et al. · Laboratory Investigation · 66

Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa1

2000 · V. Anne Westbrook, Alan B. Diekman, et al. · Biology of Reproduction · 65

Multiple areas of intestinal atresia associated with immunodeficiency and posttransfusion graft-versus-host disease

1993 · M. Whit Walker, Mark A. Lovell, et al. · The Journal of Pediatrics · 54

Loss of chromosomes 22 and 14 in the malignant progression of meningiomas

1995 · Bernard F. Schneider, Vandana Shashi, et al. · Cancer Genetics and Cytogenetics · 52

Malignant rhabdoid tumor of the kidney: Involvement of chromosome 22

1994 · Vandana Shashi, Mark A. Lovell, et al. · Genes Chromosomes and Cancer · 52

Chromosome 22q11.2 deletion in a boy with Opitz (G/BBB) syndrome

1996 · Julie S. Fryburg, Kant Y. Lin, et al. · American Journal of Medical Genetics · 50

Genetics of the low density lipoprotein receptor:

1981 · Per Magnus, Kjell Maartmann‐Moe, et al. · Clinical Genetics · 47

Mosaicism in Prader-Willi syndrome: Detection using fluorescent in situ hybridization

1999 · Wendy L. Golden, Kathy W. Sudduth, et al. · American Journal of Medical Genetics · 41

Spindle-pole organization during early mouse development

1989 · Lea Hiraoka, Wendy Golden, et al. · Developmental Biology · 40

Human fertilin β: Identification, characterization, and chromosomal mapping of an ADAM gene family member

1997 · Cecilia M. Vidaeus, Chris von Kap‐Herr, et al. · Molecular Reproduction and Development · 39

Cardiac phenotypes in chromosome 4q− syndrome with and without a deletion of the dHAND gene

2002 · Taosheng Huang, Angela E. Lin, et al. · Genetics in Medicine · 36

Distal deletion of the short arm of chromosome 6

1990 · Vickie L. Zurcher, Wendy L. Golden, et al. · American Journal of Medical Genetics · 36

Discordant phenotypes and 45,X/46,X,idic(Y).

1998 · T E Kelly, J B Franko, et al. · Journal of Medical Genetics · 35

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Genetics of the low density lipoprotein receptor:

1981 · Kjell Maartmann‐Moe, Per Magnus, et al. · Clinical Genetics · 35

Assignment of the Human Growth Hormone-Releasing Hormone Receptor Gene (GHRHR) to 7p14 by in Situ Hybridization

1994 · Bruce D. Gaylinn, Christopher von Kap-Herr, et al. · Genomics · 34

Neuropsychological capacity of prader-willi children: General and specific aspects of impairment

1986 · Stewart Gabel, Ralph E. Tarter, et al. · Applied Research in Mental Retardation · 32

Gonadoblastomas in 45,X/46,XY Mosaicism:Analysis of Y Chromosome Distribution by Fluorescence In Situ Hybridization

1997 · Julia C. Iezzoni, Christopher Von Kap-Herr, et al. · American Journal of Clinical Pathology · 31

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Clinical comparison of 59 Prader‐Willi patients with and without the 15(Q12) deletion

1987 · Sharon L. Wenger, Jeanne M. Hanchett, et al. · American Journal of Medical Genetics · 31

Are the occasional aneuploid cells in peripheral blood cultures significant?

1984 · Sharon L. Wenger, Wendy L. Golden, et al. · American Journal of Medical Genetics · 31

Molecular analysis of recombination in a family with Duchenne muscular dystrophy and a large pericentric X chromosome inversion.

1996 · V Shashi, W L Golden, et al. · PubMed · 30

Interphase Fluorescence in Situ Hybridization for Trisomy 12 on Archival Ovarian Sex Cord-Stromal Tumors

1994 · Vandana Shashi, Wendy L. Golden, et al. · Gynecologic Oncology · 28

RARA and PML gene rearrangements in acute promyelocytic leukemia with complex translocations and atypical features

1994 · Christopher D. McKinney, Michael E. Williams, et al. · Genes Chromosomes and Cancer · 28

Works count: 71

Citation count: 1,543

H-index: 26

I10-index: 39