David R. Witt

2.6k total citations
23 papers, 1.9k citations indexed

About

David R. Witt is a scholar working on Molecular Biology, Surgery and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, David R. Witt has authored 23 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Surgery and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in David R. Witt's work include Biochemical and Molecular Research (4 papers), Cystic Fibrosis Research Advances (4 papers) and Skin and Cellular Biology Research (3 papers). David R. Witt is often cited by papers focused on Biochemical and Molecular Research (4 papers), Cystic Fibrosis Research Advances (4 papers) and Skin and Cellular Biology Research (3 papers). David R. Witt collaborates with scholars based in United States, Canada and United Kingdom. David R. Witt's co-authors include K. Klinger, Anthony P. Shuber, Judith G. Hall, Garry R. Cutting, Rosemary Balfour, Robert C. Stern, Brenda Richards, Joel Skoletsky, Richard B. Parad and Henry L. Dorkin and has published in prestigious journals such as Neuron, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

David R. Witt

22 papers receiving 1.9k citations

Peers

David R. Witt

PRM

GENET

CMN

Paola Carrera Italy

L.‐C. Tsui Canada

Cyril Mignot France

Leonard Pinsky Canada

Patrick MacLeod Canada

Mordechai Shohat Israel

Mirja Somer Finland

W. Distler Germany

Maja Di Rocco Italy

Dusica Babovic‐Vuksanovic United States

Paola Carrera Italy

David R. Witt

936 ×1.3

377 ×0.6

PRM

383 ×0.9

GENET

267 ×0.9

CMN

80 ×0.4

Citations per year, relative to David R. Witt David R. Witt (= 1×) peers Paola Carrera

Countries citing papers authored by David R. Witt

Since Specialization

Citations

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

Fields of papers citing papers by David R. Witt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David R. Witt. 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 David R. Witt. The network helps show where David R. Witt may publish in the future.

Co-authorship network of co-authors of David R. Witt

This figure shows the co-authorship network connecting the top 25 collaborators of David R. Witt. A scholar is included among the top collaborators of David R. Witt 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 David R. Witt. David R. Witt 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

Dale, Beverly A., et al.. (2015). Abnormal Keratinization in Restrictive Dermopathy1. Current problems in dermatology. 17. 45–51. 1 indexed citations

Wiszniewska, Joanna, Mark Lipson, David R. Witt, et al.. (2011). Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis. Journal of Human Genetics. 56(12). 834–839. 16 indexed citations

Gijsbers, Antoinet C.J., Barbara D′haene, Yvonne Hilhorst‐Hofstee, et al.. (2008). Identification of copy number variants associated with BPES-like phenotypes. Human Genetics. 124(5). 489–498. 12 indexed citations

Kuilenburg, André B. P., Rutger Meinsma, P Boffi, et al.. (2005). Identification of three novel mutations in the dihydropyrimidine dehydrogenase gene associated with altered pre-mRNA splicing or protein function. Biological Chemistry. 386(4). 319–324. 20 indexed citations

Watson, Michael S., Garry R. Cutting, Robert J. Desnick, et al.. (2004). Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel. Genetics in Medicine. 6(5). 387–391. 315 indexed citations

Enns, Gregory M., A J Barkovich, André B. P. Kuilenburg, et al.. (2004). Head imaging abnormalities in dihydropyrimidine dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 27(4). 513–522. 17 indexed citations

Elliott, Alison M., Elizabeth Roeder, David R. Witt, David L. Rimoin, & Ralph S. Lachman. (2000). Scapuloiliac dysostosis (Kosenow syndrome, pelvis-shoulder dysplasia) spectrum: Three additional cases. American Journal of Medical Genetics. 95(5). 496–506. 8 indexed citations

Elliott, Alison M., David L. Rimoin, David R. Witt, & Ralph S. Lachman. (2000). The Scapuloiliac Dysostosis (Kosenow Syndrome) Spectrum – Two Additional Cases. Genetics in Medicine. 2(1). 77–77.

Warner, Laura E., Max J. Hilz, Stanley H. Appel, et al.. (1996). Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination. Neuron. 17(3). 451–460. 288 indexed citations

10.

Trask, B. J., Heather C. Mefford, Ger van den Engh, et al.. (1996). Quantification by flow cytometry of chromosome-17 deletions in Smith-Magenis syndrome patients. Human Genetics. 98(6). 710–718. 43 indexed citations

11.

Witt, David R., et al.. (1994). Inherited partial direct duplication of 11q: First report and possible association with a midline developmental field defect. The American Journal of Human Genetics. 55. 1 indexed citations

12.

Shohat, Mordechai, Ralph Lachman, Helen E. Gruber, et al.. (1994). Desbuquois syndrome: Clinical, radiographic, and morphologic characterization. American Journal of Medical Genetics. 52(1). 9–18. 30 indexed citations

13.

Richards, Brenda, Joel Skoletsky, Anthony P. Shuber, et al.. (1993). Multiplex PCR amplification from the CFTR gene using DNA prepared from buccal brushes/swabs. Human Molecular Genetics. 2(2). 159–163. 343 indexed citations

14.

Maçek, Milan, Claire Davis, S M Curristin, et al.. (1993). A mutation in CFTR produces different phenotypes depending on chromosomal background. Nature Genetics. 5(3). 274–278. 335 indexed citations

15.

Witt, David R., Judith Allanson, Helen E. Hughes, et al.. (1988). Bleeding diathesis in Noonan syndrome: A common association. American Journal of Medical Genetics. 31(2). 305–317. 55 indexed citations

16.

Witt, David R., H. Eugene Hoyme, Jonathan Zonana, et al.. (1987). Lymphedema in Noonan syndrome: Clues to pathogenesis and prenatal diagnosis and review of the literature. American Journal of Medical Genetics. 27(4). 841–856. 105 indexed citations

17.

Holbrook, Karen A., Beverly A. Dale, David R. Witt, Michael R. Hayden, & Helga V. Toriello. (1987). Arrested Epidermal Morphogenesis in Three Newborn Infants With a Fatal Genetic Disorder (Restrictive Dermopathy).. Journal of Investigative Dermatology. 88(3). 330–339. 37 indexed citations

18.

Witt, David R., Beth Keena, Judith G. Hall, & Judith Allanson. (1986). Growth curves for height in Noonan syndrome. Clinical Genetics. 30(3). 150–153. 77 indexed citations

19.

Witt, David R., Michael R. Hayden, Karen A. Holbrook, et al.. (1986). Restrictive dermopathy: A newly recognized autosomal recessive skin dysplasia. American Journal of Medical Genetics. 24(4). 631–648. 71 indexed citations

20.

Witt, David R. & Judith G. Hall. (1985). Approach to multiple congenital anomaly syndromes.. PubMed. 9(3). 219–31. 2 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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