Mark D. Ludman

2.4k total citations
41 papers, 1.2k citations indexed

About

Mark D. Ludman is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Mark D. Ludman has authored 41 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Molecular Biology and 9 papers in Physiology. Recurrent topics in Mark D. Ludman's work include Lysosomal Storage Disorders Research (8 papers), Genetic and Kidney Cyst Diseases (5 papers) and BRCA gene mutations in cancer (4 papers). Mark D. Ludman is often cited by papers focused on Lysosomal Storage Disorders Research (8 papers), Genetic and Kidney Cyst Diseases (5 papers) and BRCA gene mutations in cancer (4 papers). Mark D. Ludman collaborates with scholars based in Canada, United States and Israel. Mark D. Ludman's co-authors include Christopher Naugler, Duane L. Guernsey, Andrew Orr, Mathew Nightingale, Haiyan Jiang, Makoto Matsuoka, Susan C. Evans, Andrea L. Rideout, Meghan Ferguson and Dana Niehaus and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Mark D. Ludman

41 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark D. Ludman Canada 20 446 386 332 173 152 41 1.2k
Sumita Danda India 16 489 1.1× 269 0.7× 196 0.6× 111 0.6× 110 0.7× 122 1.0k
Merry Passage United States 16 366 0.8× 406 1.1× 971 2.9× 193 1.1× 322 2.1× 33 1.5k
Turgut Tükel Türkiye 14 510 1.1× 211 0.5× 730 2.2× 358 2.1× 236 1.6× 18 1.5k
Mitsuo Masuno Japan 21 1.4k 3.1× 1.1k 2.8× 212 0.6× 99 0.6× 124 0.8× 86 2.3k
Sheela Nampoothiri India 21 917 2.1× 763 2.0× 183 0.6× 251 1.5× 172 1.1× 125 1.7k
Stefano Regis Italy 22 1.2k 2.6× 169 0.4× 521 1.6× 317 1.8× 108 0.7× 57 1.9k
Katrin Õunap Estonia 25 1.0k 2.3× 857 2.2× 191 0.6× 126 0.7× 107 0.7× 106 1.8k
Anna Rajab Oman 23 1.2k 2.7× 628 1.6× 142 0.4× 454 2.6× 93 0.6× 58 1.9k
Maila Penttinen Finland 19 383 0.9× 173 0.4× 264 0.8× 98 0.6× 151 1.0× 31 920
Winnie Xin United States 18 493 1.1× 146 0.4× 348 1.0× 235 1.4× 82 0.5× 29 1.2k

Countries citing papers authored by Mark D. Ludman

Since Specialization
Citations

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

Fields of papers citing papers by Mark D. Ludman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark D. Ludman. 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 Mark D. Ludman. The network helps show where Mark D. Ludman may publish in the future.

Co-authorship network of co-authors of Mark D. Ludman

This figure shows the co-authorship network connecting the top 25 collaborators of Mark D. Ludman. A scholar is included among the top collaborators of Mark D. Ludman 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 Mark D. Ludman. Mark D. Ludman 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.
Sukenik‐Halevy, Rivka, Mark D. Ludman, Shay Ben‐Shachar, & Annick Raas‐Rothschild. (2015). The time-consuming demands of the practice of medical genetics in the era of advanced genomic testing. Genetics in Medicine. 18(4). 372–377. 33 indexed citations
2.
Cheung, Mitchell, et al.. (2013). Further evidence for germline BAP1 mutations predisposing to melanoma and malignant mesothelioma. Cancer Genetics. 206(5). 206–210. 59 indexed citations
3.
Brock, Jo‐Ann, et al.. (2012). Mosaic tetrasomy 5p resulting from an isochromosome 5p marker chromosome: Case report and review of literature. American Journal of Medical Genetics Part A. 158A(2). 406–411. 12 indexed citations
4.
Orr, Andrew, Marie‐Pierre Dubé, Juan Carlos Zenteno, et al.. (2011). Mutations in a novel serine protease PRSS56 in families with nanophthalmos.. PubMed. 17. 1850–61. 43 indexed citations
5.
Guernsey, Duane L., Haiyan Jiang, Karen Bedard, et al.. (2010). Mutation in the Gene Encoding Ubiquitin Ligase LRSAM1 in Patients with Charcot-Marie-Tooth Disease. PLoS Genetics. 6(8). e1001081–e1001081. 52 indexed citations
6.
Guernsey, Duane L., Haiyan Jiang, Susan C. Evans, et al.. (2009). Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2. The American Journal of Human Genetics. 85(1). 120–129. 61 indexed citations
7.
Guernsey, D.L., Marie‐Pierre Dubé, Haiyan Jiang, et al.. (2009). Novel mutations in the sacsin gene in ataxia patients from Maritime Canada. Journal of the Neurological Sciences. 288(1-2). 79–87. 12 indexed citations
8.
Haeuptle, Micha A., Bobby G. Ng, Jean‐Claude Michalski, et al.. (2009). RFT1 deficiency in three novel CDG patients. Human Mutation. 30(10). 1428–1434. 26 indexed citations
9.
Samuels, Mark E., Andrew Orr, Duane L. Guernsey, et al.. (2008). Is gene discovery research or diagnosis?. Genetics in Medicine. 10(6). 385–390. 6 indexed citations
10.
Byers, Peter H., Madeleine Duvic, Mary Atkinson, et al.. (1997). Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in theCOL1A1 andCOL1A2 genes of type I collagen. American Journal of Medical Genetics. 72(1). 94–105. 82 indexed citations
11.
Elliott, Alison M., Mark D. Ludman, & Ahmad S. Teebi. (1996). New syndrome?: MCA/MR syndrome with multiple circumferential skin creases. American Journal of Medical Genetics. 62(1). 23–25. 18 indexed citations
12.
Brindle, Mary & Mark D. Ludman. (1996). A structured diary to promote reflection and active learning. Academic Medicine. 71(5). 527–8. 1 indexed citations
13.
Gordon, Kevin, et al.. (1995). Successful treatment of painful crises of fabry disease with low dose morphine. Pediatric Neurology. 12(3). 250–251. 19 indexed citations
14.
Ludman, Mark D., David E. C. Cole, John F. S. Crocker, & Maimon M. Cohen. (1993). Schimke immuno‐osseous dysplasia: Case report and review. American Journal of Medical Genetics. 47(5). 793–796. 26 indexed citations
15.
Ludman, Mark D., et al.. (1993). Hypomandibular faciocranial dysostosis: Another case and review. American Journal of Medical Genetics. 47(3). 352–356. 8 indexed citations
16.
Tremblay, François, et al.. (1993). Longitudinal Study of the Early Electroretinographic Changes in Alström's Syndrome. American Journal of Ophthalmology. 115(5). 657–665. 23 indexed citations
17.
Lipton, Jeffrey M., et al.. (1992). Allogenic Bone Marrow Transplantation in Severe Gaucher Disease. Pediatric Research. 31(5). 503–507. 46 indexed citations
18.
Ludman, Mark D., et al.. (1992). GMS syndrome: A new dominant condition with goniodysgenesis, mental retardation, and short stature. American Journal of Medical Genetics. 42(1). 1–4. 3 indexed citations
19.
Ludman, Mark D., et al.. (1990). Mesomelic dysplasia with absence of fibulae and hexadactyly: Nievergelt syndrome or new syndrome?. American Journal of Medical Genetics. 37(1). 10–14. 9 indexed citations
20.
Fleshner, Phillip, et al.. (1989). Gaucher disease: Fate of the splenic remnant after partial splenectomy—A case of rapid enlargement. Journal of Pediatric Surgery. 24(6). 610–612. 11 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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