Patrick W. Kleyn

2.0k total citations
24 papers, 1.3k citations indexed

About

Patrick W. Kleyn is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Patrick W. Kleyn has authored 24 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 11 papers in Genetics and 6 papers in Genetics. Recurrent topics in Patrick W. Kleyn's work include Neurogenetic and Muscular Disorders Research (11 papers), RNA modifications and cancer (8 papers) and RNA Research and Splicing (5 papers). Patrick W. Kleyn is often cited by papers focused on Neurogenetic and Muscular Disorders Research (11 papers), RNA modifications and cancer (8 papers) and RNA Research and Splicing (5 papers). Patrick W. Kleyn collaborates with scholars based in United States, United Kingdom and Australia. Patrick W. Kleyn's co-authors include Elliot S. Vesell, T. Conrad Gilliam, Linda M. Brzustowicz, Aruna T. Bansal, Tim D. Spector, Mathias Chiano, Gail Adam, James A. Knowles, Stefan Kammerer and Christiane Honisch and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Patrick W. Kleyn

24 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
Patrick W. Kleyn United States 17 735 351 244 204 189 24 1.3k
Caroline M. Gorvin United Kingdom 21 521 0.7× 200 0.6× 41 0.2× 73 0.4× 72 0.4× 63 1.1k
Daniel M. Kemp United States 19 799 1.1× 384 1.1× 160 0.7× 113 0.6× 22 0.1× 32 1.5k
Masahiro Kaneshige Japan 19 434 0.6× 433 1.2× 21 0.1× 66 0.3× 27 0.1× 29 1.5k
David M. Flavell United Kingdom 18 848 1.2× 328 0.9× 38 0.2× 39 0.2× 25 0.1× 25 1.5k
Laurence Duprez Belgium 16 1.2k 1.6× 330 0.9× 89 0.4× 99 0.5× 111 0.6× 17 2.3k
Kenta Magoori Japan 15 555 0.8× 150 0.4× 20 0.1× 32 0.2× 35 0.2× 18 981
Vittoria Carnicelli Italy 17 457 0.6× 66 0.2× 95 0.4× 103 0.5× 113 0.6× 47 1000
E M Bailyes United Kingdom 18 668 0.9× 274 0.8× 12 0.0× 51 0.3× 47 0.2× 33 1.3k
Brendan C. Lanpher United States 17 581 0.8× 465 1.3× 57 0.2× 10 0.0× 33 0.2× 41 1.2k

Countries citing papers authored by Patrick W. Kleyn

Since Specialization
Citations

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

Fields of papers citing papers by Patrick W. Kleyn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick W. Kleyn

This figure shows the co-authorship network connecting the top 25 collaborators of Patrick W. Kleyn. A scholar is included among the top collaborators of Patrick W. Kleyn 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 W. Kleyn. Patrick W. Kleyn 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.
Sharma, Shubh D., Alastair S. Garfield, Bhavik P. Shah, et al.. (2019). Current Mechanistic and Pharmacodynamic Understanding of Melanocortin-4 Receptor Activation. Molecules. 24(10). 1892–1892. 44 indexed citations
2.
Magee, Christopher L., et al.. (2018). Pre-existing technological core and roots for the CRISPR breakthrough. PLoS ONE. 13(9). e0198541–e0198541. 10 indexed citations
3.
Wilson, Scott G., Gail Adam, Andreas Braun, et al.. (2006). Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort. European Journal of Human Genetics. 14(3). 340–348. 48 indexed citations
4.
Wilson, Scott G., Peter Reed, Aruna T. Bansal, et al.. (2003). Comparison of Genome Screens for Two Independent Cohorts Provides Replication of Suggestive Linkage of Bone Mineral Density to 3p21 and 1p36. The American Journal of Human Genetics. 72(1). 144–155. 119 indexed citations
5.
Bansal, Aruna T., Dirk van den Boom, Stefan Kammerer, et al.. (2002). Association testing by DNA pooling: An effective initial screen. Proceedings of the National Academy of Sciences. 99(26). 16871–16874. 121 indexed citations
6.
Stubdal, Hilde, Catherine Lynch, A Moriarty, et al.. (2000). Targeted Deletion of the tub Mouse Obesity Gene Reveals that tubby Is a Loss-of-Function Mutation. Molecular and Cellular Biology. 20(3). 878–882. 62 indexed citations
7.
Gu, Wei, Zhiguang Tu, Patrick W. Kleyn, et al.. (1999). Identification and functional analysis of novel human melanocortin-4 receptor variants.. Diabetes. 48(3). 635–639. 150 indexed citations
8.
Banerjee, Poulabi, Patrick W. Kleyn, James A. Knowles, et al.. (1998). TULP1 mutation in two extended Dominican kindreds with autosomal recessive Retinitis pigmentosa. Nature Genetics. 18(2). 177–179. 122 indexed citations
9.
Banerjee, Poulabi, Charles A. Lewis, Patrick W. Kleyn, et al.. (1998). Homozygosity and Physical Mapping of the Autosomal Recessive Retinitis Pigmentosa Locus (RP14) on Chromosome 6p21.3. Genomics. 48(2). 171–177. 3 indexed citations
10.
Kim, Anthony C., Luanne L. Peters, Joan H.M. Knoll, et al.. (1997). Limatin (LIMAB1), an Actin-Binding LIM Protein, Maps to Mouse Chromosome 19 and Human Chromosome 10q25, a Region Frequently Deleted in Human Cancers. Genomics. 46(2). 291–293. 29 indexed citations
11.
Boylan, Khrista, David R. Cornblath, Jonathan D. Glass, et al.. (1995). Autosomal dominant distal spinal muscular atrophy in four generations. Neurology. 45(4). 699–712. 11 indexed citations
12.
Brzustowicz, Linda M., Patrick W. Kleyn, Emilia Vitale, et al.. (1995). Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy.. PubMed. 56(1). 210–5. 15 indexed citations
13.
Kleyn, Patrick W., Emilia Vitale, B. Ross, et al.. (1995). Refinement of the spinal muscular atrophy locus by genetic and physical mapping.. PubMed. 56(1). 202–9. 25 indexed citations
14.
Brzustowicz, Linda M., Patrick W. Kleyn, James A. Knowles, et al.. (1993). Refinement of the Spinal Muscular Atrophy Locus to the Interval between D5S435 and MAP1B. Genomics. 15(2). 365–371. 58 indexed citations
15.
Brzustowicz, Linda M., Patrick W. Kleyn, Thomas Lehner, et al.. (1993). Assessment of Nonallelic Genetic Heterogeneity of Chronic (Type II and III) Spinal Muscular Atrophy. Human Heredity. 43(6). 380–387. 13 indexed citations
16.
Morrison, Karen, Patrick W. Kleyn, Ulla Bengtsson, et al.. (1993). High resolution physical map of the region surrounding the spinal muscular atrophy gene. Human Molecular Genetics. 2(8). 1169–1176. 35 indexed citations
17.
Kleyn, Patrick W., Emilia Vitale, Ji‐An Pan, et al.. (1993). Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region.. Proceedings of the National Academy of Sciences. 90(14). 6801–6805. 52 indexed citations
18.
Kleyn, Patrick W. & Thomas B. Gilliam. (1993). Progress Toward Cloning of the Gene Responsible for Childhood Spinal Muscular Atrophy. Seminars in Neurology. 13(3). 276–282. 2 indexed citations
19.
Brzustowicz, Linda M., Patrick W. Kleyn, Frederick M. Boyce, et al.. (1992). Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6. Genomics. 13(4). 991–998. 23 indexed citations
20.
Kleyn, Patrick W., Linda M. Brzustowicz, Kirk C. Wilhelmsen, et al.. (1991). Spinal muscular atrophy is not the result of mutations at the beta‐hexosaminidase or GM 2 ‐activator locus. Neurology. 41(9). 1418–1418. 4 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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