Judith P. Willner

2.0k total citations
33 papers, 1.2k citations indexed

About

Judith P. Willner is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Judith P. Willner has authored 33 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 14 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Judith P. Willner's work include Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic Syndromes and Imprinting (4 papers). Judith P. Willner is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (9 papers) and Genetic Syndromes and Imprinting (4 papers). Judith P. Willner collaborates with scholars based in United States, Switzerland and Canada. Judith P. Willner's co-authors include Robert J. Desnick, June A. Peters, Gabriela M. Baerlocher, Blanche P. Alter, Babette B. Weksler, Neelam Giri, Sharon A. Savage, Stephen J. Chanock, Peter M. Lansdorp and Bruce D. Gelb and has published in prestigious journals such as New England Journal of Medicine, Blood and Neurology.

In The Last Decade

Judith P. Willner

33 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Judith P. Willner United States 14 631 527 283 191 159 33 1.2k
Giovanni Sorge Italy 22 486 0.8× 553 1.0× 207 0.7× 153 0.8× 60 0.4× 75 1.3k
Rena E. Falk United States 19 408 0.6× 447 0.8× 85 0.3× 174 0.9× 121 0.8× 39 1.0k
Katrin Õunap Estonia 25 1.0k 1.6× 857 1.6× 191 0.7× 264 1.4× 72 0.5× 106 1.8k
Kenzo Takeshita Japan 21 433 0.7× 223 0.4× 225 0.8× 272 1.4× 131 0.8× 110 1.4k
Hubert Journel France 23 563 0.9× 559 1.1× 82 0.3× 191 1.0× 39 0.2× 57 1.4k
Cyril Mignot France 26 844 1.3× 464 0.9× 520 1.8× 79 0.4× 79 0.5× 101 2.0k
Emmanuelle Lemyre Canada 22 550 0.9× 879 1.7× 90 0.3× 276 1.4× 55 0.3× 52 1.3k
David R. Witt United States 17 694 1.1× 444 0.8× 101 0.4× 186 1.0× 36 0.2× 23 1.9k
Yong Seung Hwang South Korea 22 553 0.9× 213 0.4× 114 0.4× 284 1.5× 71 0.4× 89 1.4k
Erawati V. Bawle United States 17 562 0.9× 442 0.8× 40 0.1× 229 1.2× 72 0.5× 38 1.1k

Countries citing papers authored by Judith P. Willner

Since Specialization
Citations

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

Fields of papers citing papers by Judith P. Willner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Judith P. Willner. 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 Judith P. Willner. The network helps show where Judith P. Willner may publish in the future.

Co-authorship network of co-authors of Judith P. Willner

This figure shows the co-authorship network connecting the top 25 collaborators of Judith P. Willner. A scholar is included among the top collaborators of Judith P. Willner 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 Judith P. Willner. Judith P. Willner 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.
Soorya, Latha, A lexander Kolevzon, Jessica Zweifach, et al.. (2013). Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency. Molecular Autism. 4(1). 18–18. 236 indexed citations
2.
Gentile, Ronald C., et al.. (2010). Choroideremia in a woman with ectodermal dysplasia and complex translocations involving chromosomes X, 1, and 3. Ophthalmic Genetics. 31(4). 178–182. 11 indexed citations
3.
Kolevzon, A lexander, Guiqing Cai, Latha Soorya, et al.. (2010). Analysis of a purported SHANK3 mutation in a boy with autism: Clinical impact of rare variant research in neurodevelopmental disabilities. Brain Research. 1380. 98–105. 25 indexed citations
4.
Alter, Blanche P., Gabriela M. Baerlocher, Sharon A. Savage, et al.. (2007). Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita. Blood. 110(5). 1439–1447. 248 indexed citations
5.
Shin, Helen T., Amy S. Paller, George Hoganson, et al.. (2004). Infantile systemic hyalinosis. Journal of the American Academy of Dermatology. 50(2). 61–64. 29 indexed citations
6.
Ben‐Yosef, Tamar, Seth Ness, Anne C. Madeo, et al.. (2003). A Mutation ofPCDH15among Ashkenazi Jews with the Type 1 Usher Syndrome. New England Journal of Medicine. 348(17). 1664–1670. 71 indexed citations
7.
Zaslav, Ann‐Leslie, et al.. (2000). Prenatal diagnosis of trisomy 4 mosaicism. American Journal of Medical Genetics. 95(4). 381–384. 11 indexed citations
8.
Willner, Judith P.. (2000). Genetic Evaluation and Counseling in Head and Neck Syndromes. Otolaryngologic Clinics of North America. 33(6). 1159–1169. 4 indexed citations
9.
Cotter, Philip D., Arvind Babu, Judith P. Willner, & Robert J. Desnick. (1998). Prenatal diagnosis and outcome of mosaicism for ade novo unbalanced translocation identified in amniocytes. Prenatal Diagnosis. 18(8). 857–861. 2 indexed citations
10.
Gelb, Bruce D., Judith P. Willner, Teresa Dunn, et al.. (1998). Paternal Uniparental Disomy for Chromosome 1 Revealed by Molecular Analysis of a Patient with Pycnodysostosis. The American Journal of Human Genetics. 62(4). 848–854. 58 indexed citations
11.
Rhodes, Rosamond, Judith P. Willner, Kurt Hirschhorn, et al.. (1998). Issues in Medical Ethics. DigitalGeorgetown (Georgetown University Library). 4 indexed citations
12.
Cotter, Philip D., et al.. (1997). Paternal uniparental disomy for chromosome 14: A case report and review. American Journal of Medical Genetics. 70(1). 74–79. 83 indexed citations
13.
Babu, Arvind, et al.. (1997). Mosaicism for a small supernumerary ring X chromosome in a dysmorphic, growth‐retarded male: mos47,XXY/48,XXY, + r(X). Clinical Genetics. 52(6). 432–435. 9 indexed citations
14.
Cotter, Philip D., et al.. (1997). Prenatal detection and molecular characterization of a de novo duplication of the distal long arm of chromosome 19. American Journal of Medical Genetics. 71(3). 325–328. 13 indexed citations
15.
Cotter, Philip D., Michele Caggana, Judith P. Willner, Arvind Babu, & Robert J. Desnick. (1996). Prenatal diagnosis of a fetus with two balanced de novo chromosome rearrangements. American Journal of Medical Genetics. 66(2). 197–199. 7 indexed citations
16.
Pastores, Gregory M., Filippo M. Santorelli, Sara Shanske, et al.. (1994). Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G). American Journal of Medical Genetics. 50(3). 265–271. 99 indexed citations
17.
Ghidini, Alessandro, et al.. (1993). Prenatal detection of monosomy 21 mosaicism. Prenatal Diagnosis. 13(3). 163–169. 11 indexed citations
18.
Richkind, K, et al.. (1991). Prenatal diagnosis and outcomes of five cases of mosaicism for an isochromosome of 20q. Prenatal Diagnosis. 11(6). 371–376. 7 indexed citations
19.
Willner, Judith P., Gregory A. Grabowski, Ronald E. Gordon, Adam N. Bender, & Robert J. Desnick. (1981). Chronic GM 2 gangliosidosis masquerading as atypical Friedreich ataxia. Neurology. 31(7). 787–787. 62 indexed citations
20.
Brill, Charles B., et al.. (1978). Spastic quadriparesis due to C1–C2 subluxation in hurler syndrome. The Journal of Pediatrics. 92(3). 441–443. 35 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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