Patrick L. Wilmot

405 total citations
26 papers, 238 citations indexed

About

Patrick L. Wilmot is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Patrick L. Wilmot has authored 26 papers receiving a total of 238 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Surgery. Recurrent topics in Patrick L. Wilmot's work include Genetics and Neurodevelopmental Disorders (14 papers), Genomic variations and chromosomal abnormalities (7 papers) and Congenital Anomalies and Fetal Surgery (6 papers). Patrick L. Wilmot is often cited by papers focused on Genetics and Neurodevelopmental Disorders (14 papers), Genomic variations and chromosomal abnormalities (7 papers) and Congenital Anomalies and Fetal Surgery (6 papers). Patrick L. Wilmot collaborates with scholars based in United States. Patrick L. Wilmot's co-authors include Lawrence R. Shapiro, Patricia D. Murphy, Peter A. Duncan, Seymour Levine, W. Roy Breg, Robert M. Klein, Muhammad Choudhury, Jen Wei Chiao, Majid Eshghi and Joseph C. Addonizio and has published in prestigious journals such as Genetics, The Journal of Pediatrics and Urology.

In The Last Decade

Patrick L. Wilmot

25 papers receiving 232 citations

Peers

Patrick L. Wilmot

GENET

PPCH

Sonia Nizard France

Heide Seidel Germany

Jean‐Pierre Fryns Belgium

Jack H. Jung Canada

Lorraine Gaunt United Kingdom

Marie‐Louise Bondeson Sweden

M E Oude Luttikhuis United Kingdom

Jacquelyn Roberson United States

Emma Hobson United Kingdom

C. Schaap Netherlands

Sonia Nizard France

Patrick L. Wilmot

227 ×1.5

GENET

131 ×1.4

87 ×1.8

PPCH

17 ×0.5

21 ×0.7

Citations per year, relative to Patrick L. Wilmot Patrick L. Wilmot (= 1×) peers Sonia Nizard

Countries citing papers authored by Patrick L. Wilmot

Since Specialization

Citations

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

Fields of papers citing papers by Patrick L. Wilmot

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick L. Wilmot

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick L. Wilmot. A scholar is included among the top collaborators of Patrick L. Wilmot 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 Patrick L. Wilmot. Patrick L. Wilmot is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Shapiro, Lawrence R., Richard J. Simensen, Patrick L. Wilmot, et al.. (1994). Asymmetry of methylation with FMR‐1 full mutation in two 45,X/46,XX mosaic females associated with normal intellect. American Journal of Medical Genetics. 51(4). 507–508. 7 indexed citations

Wilmot, Patrick L., et al.. (1993). Kallmann syndrome associated with complex chromosome rearrangement. American Journal of Medical Genetics. 45(5). 539–541. 15 indexed citations

Shapiro, Lawrence R., Patrick L. Wilmot, & Gene S. Fisch. (1992). Prenatal cytogenetic diagnosis of the fragile X syndrome in amniotic fluid: Calculation of accuracy. American Journal of Medical Genetics. 43(1-2). 170–173. 2 indexed citations

Shapiro, Lawrence R., et al.. (1992). Prenatal cytogenetic diagnosis of the fragile X chromosome: Feasibility and speed of in situ clonal method in amniotic fluid cell tissue culture. American Journal of Medical Genetics. 43(1-2). 167–169. 2 indexed citations

Murphy, Patricia D., Patrick L. Wilmot, & Lawrence R. Shapiro. (1992). Prenatal diagnosis of fragile X syndrome: Results from parallel molecular and cytogenetic studies. American Journal of Medical Genetics. 43(1-2). 181–186. 2 indexed citations

Shapiro, Lawrence R., et al.. (1991). Cytogenetic diagnosis of the fragile X syndrome: Efficiency, utilization, and trends. American Journal of Medical Genetics. 38(2-3). 408–410. 4 indexed citations

Murphy, Patricia D., M. Watson, Lawrence R. Shapiro, Patrick L. Wilmot, & W. Roy Breg. (1991). DNA‐based genetic testing in fifty fragile X families. American Journal of Medical Genetics. 38(2-3). 305–310. 2 indexed citations

Shapiro, Lawrence R., Patrick L. Wilmot, & Patricia D. Murphy. (1991). Prenatal diagnosis of the fragile X syndrome: Possible end of the experimental phase for amniotic fluid. American Journal of Medical Genetics. 38(2-3). 453–455. 6 indexed citations

Shapiro, Lawrence R., et al.. (1991). Prader‐Willi syndrome and Robertsonian translocations involving chromosome 15. Clinical Genetics. 39(4). 294–297. 6 indexed citations

10.

Wilmot, Patrick L., et al.. (1990). Disomic balanced reciprocal translocation. Clinical Genetics. 38(2). 126–127. 12 indexed citations

11.

Addonizio, Joseph C., Muhammad Choudhury, Majid Eshghi, et al.. (1990). Establishment of new human prostatic cancer cell line (JCA-I). Urology. 36(1). 79–84. 44 indexed citations

12.

Wilmot, Patrick L., et al.. (1990). Deletion of 16q with prolonged survival and unusual radiographic manifestations. American Journal of Medical Genetics. 37(4). 504–509. 16 indexed citations

13.

Wilmot, Patrick L., et al.. (1989). Trisomy 5 mosaicism in amniotic fluid with normal outcome. Clinical Genetics. 35(4). 282–284. 9 indexed citations

14.

Butler, Merlin G., Dinesh Shah, Patrick L. Wilmot, et al.. (1988). The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis. American Journal of Medical Genetics. 31(4). 775–778. 1 indexed citations

15.

Shapiro, Lawrence R., Patrick L. Wilmot, Patricia D. Murphy, & W. Roy Breg. (1988). Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: Amniotic fluid, chorionic villi, fetal blood and molecular methods. American Journal of Medical Genetics. 30(1-2). 347–354. 15 indexed citations

16.

Weinstein, Martha, Alyssa Grossman, Mary Ann Perle, et al.. (1988). The karyotype of Philadelphia chromosome-negative, bcr rearrangement-positive chronic myeloid leukemia. Cancer Genetics and Cytogenetics. 35(2). 223–229. 10 indexed citations

17.

Shapiro, Lawrence R., et al.. (1987). PRENATAL PATHOGENESIS OF MACROORCHIDISM IN THE FRAGILE X SYNDROME. Pediatric Research. 21(4). 230A–230A. 1 indexed citations

18.

Shapiro, Lawrence R., et al.. (1984). Pericentric inversion of the Y chromosome and prenatal diagnosis. Prenatal Diagnosis. 4(6). 463–465. 14 indexed citations

19.

Shapiro, Lawrence R. & Patrick L. Wilmot. (1984). PRENATAL DIAGNOSIS OF THE FRAGILE X CHROMOSOME. Pediatric Research. 18. 225A–225A. 3 indexed citations

20.

Wilmot, Patrick L., et al.. (1973). Genetic control of two esterase enzymes in Peromyscus leucopus. Journal of Heredity. 64(1). 43–44. 3 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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