Golder N. Wilson

4.5k total citations
117 papers, 3.1k citations indexed

About

Golder N. Wilson is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Golder N. Wilson has authored 117 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 64 papers in Genetics, 59 papers in Molecular Biology and 20 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Golder N. Wilson's work include Genomic variations and chromosomal abnormalities (27 papers), Prenatal Screening and Diagnostics (14 papers) and Congenital heart defects research (12 papers). Golder N. Wilson is often cited by papers focused on Genomic variations and chromosomal abnormalities (27 papers), Prenatal Screening and Diagnostics (14 papers) and Congenital heart defects research (12 papers). Golder N. Wilson collaborates with scholars based in United States, Canada and United Kingdom. Golder N. Wilson's co-authors include Roy D. Schmickel, Amiya K. Hajra, Mark Krystal, Norman Arnheim, E. A. Zimmer, Oliver A. Ryder, Roy Schmickel, Nabanita S. Datta, Jeanne M. Erickson and John M. Opitz and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Golder N. Wilson

116 papers receiving 2.9k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Golder N. Wilson United States 29 1.8k 1.3k 465 428 339 117 3.1k
Michele D’Urso Italy 35 2.8k 1.6× 1.4k 1.1× 706 1.5× 423 1.0× 283 0.8× 100 4.2k
Moshe Frydman Israel 37 2.4k 1.3× 1.4k 1.0× 239 0.5× 208 0.5× 310 0.9× 132 4.6k
Roy D. Schmickel United States 28 2.4k 1.4× 1.1k 0.8× 315 0.7× 429 1.0× 224 0.7× 50 3.4k
Jürgen Horst Germany 27 1.7k 1.0× 1.1k 0.8× 330 0.7× 142 0.3× 146 0.4× 74 2.9k
Damien Sanlaville France 33 1.6k 0.9× 2.2k 1.6× 585 1.3× 385 0.9× 356 1.1× 189 3.7k
E. Viégas-Pèquignot France 33 4.2k 2.4× 2.0k 1.5× 587 1.3× 810 1.9× 225 0.7× 92 6.0k
Eric Seboun United States 12 1.8k 1.0× 1.3k 1.0× 176 0.4× 298 0.7× 243 0.7× 24 3.9k
F.F.B. Elder United States 31 2.1k 1.2× 2.2k 1.7× 367 0.8× 667 1.6× 361 1.1× 76 3.9k
Karen Brøndum‐Nielsen Denmark 34 2.3k 1.3× 2.0k 1.5× 485 1.0× 290 0.7× 233 0.7× 137 4.1k
Meredith Wilson Australia 31 1.6k 0.9× 1.1k 0.8× 342 0.7× 104 0.2× 478 1.4× 92 3.3k

Countries citing papers authored by Golder N. Wilson

Since Specialization
Citations

This map shows the geographic impact of Golder N. Wilson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Golder N. Wilson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Golder N. Wilson more than expected).

Fields of papers citing papers by Golder N. Wilson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Golder N. Wilson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Golder N. Wilson. The network helps show where Golder N. Wilson may publish in the future.

Co-authorship network of co-authors of Golder N. Wilson

This figure shows the co-authorship network connecting the top 25 collaborators of Golder N. Wilson. A scholar is included among the top collaborators of Golder N. Wilson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Golder N. Wilson. Golder N. Wilson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Wilson, Golder N., et al.. (2025). Similar Ehlers–Danlos Syndrome Profiles Produced by Variants in Multiple Collagen Genes. SHILAP Revista de lepidopterología. 5(1). 11–11.
2.
Wilson, Golder N.. (2023). A Clinical Qualification Protocol Highlights Overlapping Genomic Influences and Neuro-Autonomic Mechanisms in Ehlers–Danlos and Long COVID-19 Syndromes. Current Issues in Molecular Biology. 45(7). 6003–6023. 5 indexed citations
3.
Wilson, Golder N. & Vijay S. Tonk. (2018). Autism: A Different Vision. Open Journal of Psychiatry. 8(3). 263–296. 2 indexed citations
4.
Rakheja, Dinesh, Golder N. Wilson, & Beverly Barton Rogers. (2003). Biochemical Abnormality Associated with Smith-Lemli-Opitz Syndrome in an Infant with Features of Rutledge Multiple Congenital Anomaly Syndrome Confirms that the Latter is a Variant of the Former. Pediatric and Developmental Pathology. 6(3). 270–277. 3 indexed citations
5.
Wilson, Golder N., et al.. (2003). Behavioral assessment of children with Down syndrome using the Reiss psychopathology scale. American Journal of Medical Genetics Part A. 118A(3). 210–216. 46 indexed citations
6.
Wilson, Golder N., et al.. (1999). Down syndrome: Perinatal complications and counseling experiences in 216 patients. American Journal of Medical Genetics. 89(2). 96–99. 36 indexed citations
7.
Wilson, Golder N., et al.. (1994). Structure and Expression of Mammalian Peroxisome Assembly Factor-1 (PMP35) Genes. Biochemical Medicine and Metabolic Biology. 51(2). 140–148. 4 indexed citations
8.
Vits, Lieve, Guy Van Camp, Paul Coucke, et al.. (1994). MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM. Nature Genetics. 7(3). 408–413. 110 indexed citations
9.
Wilson, Golder N., et al.. (1992). Non-specific X linked mental retardation with aphasia exhibiting genetic linkage to chromosomal region Xp11.. Journal of Medical Genetics. 29(9). 629–634. 14 indexed citations
10.
Wilson, Golder N., et al.. (1991). Structure and variability of mammalian peroxisomal membrane proteins. Biochemical Medicine and Metabolic Biology. 46(2). 235–245. 5 indexed citations
11.
Wilson, Golder N., et al.. (1991). Maternal Clofibrate Administration Amplifies Fetal Peroxisomes. Pediatric Research. 29(3). 256–262. 22 indexed citations
12.
Wilson, Golder N., Robert H. Squires, & Arthur G. Weinberg. (1991). Keratitis, hepatitis, ichthyosis, and deafness: Report and review of KID syndrome. American Journal of Medical Genetics. 40(3). 255–259. 32 indexed citations
13.
Kaplan, Paige, et al.. (1990). Malformations and minor anomalies in children whose mothers had prenatal diagnosis: Comparison between CVS and amniocentesis. American Journal of Medical Genetics. 37(3). 366–370. 46 indexed citations
14.
Wilson, Golder N. & A. Al Saadi. (1989). Obesity and abnormal behaviour associated with interstitial deletion of chromosome 18 (q12.2q21.1).. Journal of Medical Genetics. 26(1). 62–63. 21 indexed citations
15.
Wilson, Golder N., Jean‐Pierre de Chadarévian, Paige Kaplan, et al.. (1989). Glutaric aciduria type II: Review of the phenotype and report of an unusual glomerulopathy. American Journal of Medical Genetics. 32(3). 395–401. 27 indexed citations
16.
Wilson, Golder N., Majed Dasouki, Mason Barr, John M. Opitz, & James F. Reynolds. (1986). Occurrence of holoprosencephaly in chromosome 13 disorders cannot be explained by duplication/deficiency of a single locus. American Journal of Medical Genetics. 25(S2). 65–72. 12 indexed citations
17.
Dafoe, Donald C., Darrell A. Campbell, William H. Marks, Golder N. Wilson, & Jeremiah G. Turcotte. (1985). KARYOTYPIC CHIMERISM AND REJECTION IN A PANCREATICODUODENOSPLENIC TRANSPLANT. Transplantation. 40(5). 572–573. 3 indexed citations
18.
Erickson, Jeanne M., et al.. (1981). Structure and variation of human ribosomal DNA: molecular analysis of cloned fragments. Gene. 16(1-3). 1–9. 222 indexed citations
19.
Wilson, Golder N., Virginia Hieber, & Roy D. Schmickel. (1978). The association of chromosome 3 duplication and the Correlia de Lange syndrome. The Journal of Pediatrics. 93(5). 783–788. 63 indexed citations
20.
Anderson, W.F., Jane E. Barker, Norton A. Elson, et al.. (1975). Activation and inactivation of genes determining hemoglobin types. Journal of Cellular Physiology. 85(S1). 477–494. 4 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Michele D’Urso Breakdown of academic impact, for papers by Moshe Frydman Breakdown of academic impact, for papers by Roy D. Schmickel Breakdown of academic impact, for papers by Jürgen Horst Breakdown of academic impact, for papers by Damien Sanlaville Breakdown of academic impact, for papers by E. Viégas-Pèquignot Breakdown of academic impact, for papers by Eric Seboun Breakdown of academic impact, for papers by F.F.B. Elder Breakdown of academic impact, for papers by Karen Brøndum‐Nielsen Breakdown of academic impact, for papers by Meredith Wilson
Rankless by CCL
2026