Wendy L. Golden

2.2k total citations
63 papers, 1.7k citations indexed

About

Wendy L. Golden is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Wendy L. Golden has authored 63 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 22 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Wendy L. Golden's work include Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (10 papers) and Migraine and Headache Studies (7 papers). Wendy L. Golden is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Prenatal Screening and Diagnostics (10 papers) and Migraine and Headache Studies (7 papers). Wendy L. Golden collaborates with scholars based in United States, Norway and Netherlands. Wendy L. Golden's co-authors include Marcelo E. Bigal, Richard B. Lipton, Dawn C. Buse, Matthew S. Robbins, Tobias Kurth, Nancy C. Santanello, Vandana Shashi, C. Von Kap-Herr, Thaddeus E. Kelly and Julie S. Fryburg and has published in prestigious journals such as Blood, Neurology and Developmental Biology.

In The Last Decade

Wendy L. Golden

62 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wendy L. Golden United States 25 642 393 364 312 249 63 1.7k
Alan M. McGregor United Kingdom 25 280 0.4× 295 0.8× 289 0.8× 259 0.8× 168 0.7× 47 2.2k
Carlo Fusco Italy 21 565 0.9× 258 0.7× 353 1.0× 323 1.0× 122 0.5× 118 1.8k
Sylvie Brailly‐Tabard France 34 900 1.4× 708 1.8× 113 0.3× 369 1.2× 161 0.6× 87 3.1k
G. Tolis Greece 31 487 0.8× 238 0.6× 105 0.3× 417 1.3× 132 0.5× 137 3.4k
Clifford J. Rosen United States 27 1.1k 1.7× 339 0.9× 86 0.2× 172 0.6× 218 0.9× 61 2.7k
Ali S. Çalıkoğlu United States 19 380 0.6× 317 0.8× 68 0.2× 165 0.5× 363 1.5× 44 1.6k
Marcia Wilkinson United Kingdom 24 422 0.7× 249 0.6× 370 1.0× 661 2.1× 667 2.7× 49 2.4k
George E. Farmer United States 17 957 1.5× 206 0.5× 76 0.2× 170 0.5× 106 0.4× 41 2.2k
P. Fioretti Italy 27 241 0.4× 423 1.1× 99 0.3× 242 0.8× 255 1.0× 133 2.2k
Michael Bliziotes United States 22 466 0.7× 139 0.4× 125 0.3× 216 0.7× 321 1.3× 36 1.5k

Countries citing papers authored by Wendy L. Golden

Since Specialization
Citations

This map shows the geographic impact of Wendy L. Golden'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 Wendy L. Golden with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wendy L. Golden more than expected).

Fields of papers citing papers by Wendy L. Golden

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wendy L. Golden. 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 Wendy L. Golden. The network helps show where Wendy L. Golden may publish in the future.

Co-authorship network of co-authors of Wendy L. Golden

This figure shows the co-authorship network connecting the top 25 collaborators of Wendy L. Golden. A scholar is included among the top collaborators of Wendy L. Golden 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 Wendy L. Golden. Wendy L. Golden 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.
Yuan, Huiling, Fujun Qin, Mercedeh Movassagh, et al.. (2013). A Chimeric RNA Characteristic of Rhabdomyosarcoma in Normal Myogenesis Process. Cancer Discovery. 3(12). 1394–1403. 65 indexed citations
2.
Hu, Xiaohan, Wendy L. Golden, S. Bolge, et al.. (2010). Predictability of Future Attacks by Migraineurs: A Prospective Observational Study. Headache The Journal of Head and Face Pain. 50(8). 1296–1305. 11 indexed citations
3.
Huang, Taosheng, Angela E. Lin, Gerald F. Cox, et al.. (2002). Cardiac phenotypes in chromosome 4q− syndrome with and without a deletion of the dHAND gene. Genetics in Medicine. 4(6). 464–467. 29 indexed citations
4.
Brown, Kenneth G., et al.. (2001). Repurposing instructor-led training into Web-based training: a case study and lessons learned. 17(1). 415–422.
5.
Westbrook, V. Anne, Alan B. Diekman, Ken Klotz, et al.. (2000). Spermatid-Specific Expression of the Novel X-Linked Gene Product SPAN-X Localized to the Nucleus of Human Spermatozoa1. Biology of Reproduction. 63(2). 469–481. 53 indexed citations
6.
Guo, Tian‐Zhi, Lawrence Poree, Wendy L. Golden, et al.. (1996). Antinociceptive Response to Nitrous Oxide Is Mediated by Supraspinal Opiate and Spinal α2Adrenergic Receptors in the Rat. Anesthesiology. 85(4). 846–852. 84 indexed citations
7.
Shashi, Vandana, et al.. (1996). Constellation of congenital abnormalities in an infant: A new syndrome or tissue-specific mosaicism for trisomy 18?. American Journal of Medical Genetics. 62(1). 38–41. 2 indexed citations
8.
Shashi, Vandana, et al.. (1995). Loss of chromosomes 22 and 14 in the malignant progression of meningiomas. Cancer Genetics and Cytogenetics. 85(2). 101–104. 47 indexed citations
9.
Gaylinn, Bruce D., et al.. (1994). Assignment of the Human Growth Hormone-Releasing Hormone Receptor Gene (GHRHR) to 7p14 by in Situ Hybridization. Genomics. 19(1). 193–195. 20 indexed citations
10.
Shashi, Vandana, et al.. (1994). Malignant rhabdoid tumor of the kidney: Involvement of chromosome 22. Genes Chromosomes and Cancer. 10(1). 49–54. 46 indexed citations
11.
Williams, Michael E., et al.. (1994). RARA and PML gene rearrangements in acute promyelocytic leukemia with complex translocations and atypical features. Genes Chromosomes and Cancer. 9(1). 49–56. 26 indexed citations
12.
Golden, Wendy L., C. Von Kap-Herr, Barbara E. Kurth, et al.. (1993). Refinement of the Localization of the Gene for Human Intra-acrosomal Protein SP-10 (ACRV1) to the Junction of Bands q23→ q24 of Chromosome 11 by Nonisotopic in Situ Hybridization. Genomics. 18(2). 446–449. 15 indexed citations
13.
Fryburg, Julie S. & Wendy L. Golden. (1993). Interstitial deletion of 8q13.3→ 22.1 associated with craniosynostosis. American Journal of Medical Genetics. 45(5). 638–641. 9 indexed citations
14.
Walker, M. Whit, Mark A. Lovell, Thaddeus E. Kelly, Wendy L. Golden, & Frank T. Saulsbury. (1993). Multiple areas of intestinal atresia associated with immunodeficiency and posttransfusion graft-versus-host disease. The Journal of Pediatrics. 123(1). 93–95. 31 indexed citations
15.
Kap-Herr, C. Von, Thaddeus E. Kelly, & Wendy L. Golden. (1992). Uncultured blood smears hybridized with alpha satellite probes to diagnose 45,X in spontaneously aborted fetuses. American Journal of Medical Genetics. 44(3). 394–397. 6 indexed citations
16.
Gustashaw, Karen M., et al.. (1991). Diagnosis of tetrasomy 18p using in situ hybridization of a DNA probe to metaphase chromosomes. American Journal of Medical Genetics. 41(2). 180–183. 8 indexed citations
17.
Wenger, Sharon L., et al.. (1987). Clinical comparison of 59 Prader‐Willi patients with and without the 15(Q12) deletion. American Journal of Medical Genetics. 28(4). 881–887. 25 indexed citations
18.
Schneider, Bernard F. & Wendy L. Golden. (1986). Acquisition of acoustic startle shows a dose‐response to serum free T4. International Journal of Developmental Neuroscience. 4(4). 397–400. 8 indexed citations
19.
Gabel, Stewart, et al.. (1986). Neuropsychological capacity of prader-willi children: General and specific aspects of impairment. Applied Research in Mental Retardation. 7(4). 459–466. 24 indexed citations
20.
Golden, Wendy L., et al.. (1980). The MZ half-sib design: an approach for the examination of the etiology of congenital malformations.. PubMed. 46. 437–54. 5 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.

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