Golder N. Wilson - Concepedia

Author

Golder N. Wilson

The University of Texas Southwestern Medical Center ORCID

Also Known As

G N Wilson, G Wilson, G. N. Wilson, G. Wilson, G.N. Wilson, GOLDER N. WILSON, Golder N Wilson, Golder N. Wilson, Golder Wilson, Golder N. Wilson

233

Publications

4.5K

Citations

H-Index

121

Concepts

All Affiliations

The University of Texas Southwestern Medical Center University of Michigan Texas Tech University Texas Tech University Health Sciences Center Radboud University Nijmegen

About

Golder N. Wilson is an author at The University of Texas Southwestern Medical Center specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	38	2.5K
2	Natural Sciences	6	6	685
3	Public Health	2	2	77
4	Arts	1	1	10
5	Nursing	1	1	44

Golder N. Wilson

Publications

3.9K

Citations

H-Index

Page 1

	Year	Citations
Molecular evidence for genetic exchanges among ribosomal genes on nonhomologous chromosomes in man and apes. Norman Arnheim, Mark Krystal, Roy Schmickel, Proceedings of the National Academy of Sciences CytogeneticsGeneticsNatural SelectionMolecular GeneticsPrimate Systematics	1980	454
Structure and variation of human ribosomal DNA: molecular analysis of cloned fragments Jeanne M. Erickson, CAROLINE L. RUSHFORD, D J Dorney, Gene Dna SequencingGeneticsMolecular AnalysisDna AnalysisMolecular Biology	1981	235
Holoprosencephaly in infants of diabetic mothers Mason Barr, James W. Hanson, Kathleen M. Currey, The Journal of Pediatrics MedicineDiabetesPediatricsMaternal HealthGestational Diabetes	1983	218
Deficiency of Enzymes Catalyzing the Biosynthesis of Glycerol-Ether Lipids in Zellweger Syndrome Nabanita S. Datta, Golder N. Wilson, Amiya K. Hajra New England Journal of Medicine	1984	188
MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM Lieve Vits, Guy Van Camp, Paul Coucke, Nature Genetics Molecular NeuroscienceMendelian DisorderGenetic DisorderMedicinePathology	1994	154
Zellweger syndrome: Diagnostic assays, syndrome delineation, and potential therapy Golder N. Wilson, Ronald G. Holmes, Joseph R. Custer, American Journal of Medical Genetics	1986	145
Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features Emma Tham, Anna Lindstrand, Avni Santani, The American Journal of Human Genetics Recognizable Syndromic FeaturesDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2015	140
The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin–Siris syndrome Pleuntje J. van der Sluijs, Sandra Jansen, Samantha A. Schrier Vergano, Genetics in Medicine	2018	127
The frequency of aneuploidy in cultured lymphocytes is correlated with age and gender but not with reproductive history. Gregory P Nowinski, Daniel L. Van Dyke, B Tilley, PubMed	1990	126
The Kabuki (Niikawa-Kuroki) syndrome: further delineation of the phenotype in 29 non-Japanese patients C. T. R. M. Schrander‐Stumpel, Peter Meinecke, Golder N. Wilson, European Journal of Pediatrics MedicineFurther DelineationPathologyNeurologyNon-japanese Patients	1994	116

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