Daniel H. Cohn

13.1k total citations · 1 hit paper
142 papers, 7.3k citations indexed

About

Daniel H. Cohn is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Daniel H. Cohn has authored 142 papers receiving a total of 7.3k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Genetics, 88 papers in Molecular Biology and 36 papers in Rheumatology. Recurrent topics in Daniel H. Cohn's work include Connective tissue disorders research (79 papers), Cell Adhesion Molecules Research (28 papers) and Osteoarthritis Treatment and Mechanisms (22 papers). Daniel H. Cohn is often cited by papers focused on Connective tissue disorders research (79 papers), Cell Adhesion Molecules Research (28 papers) and Osteoarthritis Treatment and Mechanisms (22 papers). Daniel H. Cohn collaborates with scholars based in United States, Canada and Czechia. Daniel H. Cohn's co-authors include David L. Rimoin, Deborah Krakow, Peter H. Byers, William R. Wilcox, Ralph S. Lachman, Andrea Superti‐Furga, Douglas J. Wilkin, David R. Eyre, Matthew L. Warman and Patricia L. Tavormina and has published in prestigious journals such as Science, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Daniel H. Cohn

140 papers receiving 7.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Nosology and classification of genetic skeletal disorders: 2019 revision

2019 379 citations Daniel H. Cohn, Deborah Krakow et al. profile →

Peers

Daniel H. Cohn

GENET

RHEUM

ONCOL

Bernhard Zabel Germany

Deborah Krakow United States

Kathryn S.E. Cheah Hong Kong

John F. Bateman Australia

Paul Coucke Belgium

Linda J. Sandell United States

Ray Boot-Handford United Kingdom

Véronique Lefebvre United States

Shintaro Nomura Japan

Andreas Schedl France

Bernhard Zabel Germany

Daniel H. Cohn

4.7k ×1.2

GENET

7.2k ×1.8

1.5k ×0.9

RHEUM

620 ×0.7

1.3k ×1.6

ONCOL

Citations per year, relative to Daniel H. Cohn Daniel H. Cohn (= 1×) peers Bernhard Zabel

Countries citing papers authored by Daniel H. Cohn

Since Specialization

Citations

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

Fields of papers citing papers by Daniel H. Cohn

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel H. Cohn. 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 Daniel H. Cohn. The network helps show where Daniel H. Cohn may publish in the future.

Co-authorship network of co-authors of Daniel H. Cohn

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel H. Cohn. A scholar is included among the top collaborators of Daniel H. Cohn 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 Daniel H. Cohn. Daniel H. Cohn 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

Csukasi, Fabiana, Michaela Kunova Bosakova, Jorge Martı́n, et al.. (2020). Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia. EBioMedicine. 62. 103075–103075. 9 indexed citations

Csukasi, Fabiana, Iván Durán, Tomáš Bárta, et al.. (2018). The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling. Science Translational Medicine. 10(459). 41 indexed citations

Durán, Iván, Jorge Martı́n, Mary Ann Weis, et al.. (2017). A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen. Journal of Bone and Mineral Research. 32(6). 1309–1319. 56 indexed citations

Zhang, Wenjuan, S. Paige Taylor, Iván Durán, et al.. (2017). Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies. Human Mutation. 39(1). 152–166. 83 indexed citations

Byers, Peter H., Richard Wenstrup, Jeffrey Bonadio, Barbra J. Starman, & Daniel H. Cohn. (2015). Molecular Basis of Inherited Disorders of Collagen Biosynthesis: Implications for Prenatal Diagnosis1. Current problems in dermatology. 16. 158–174.

Weinstein, Michael M., Stuart W. Tompson, Yuqing Chen, Brendan Lee, & Daniel H. Cohn. (2014). Mice Expressing Mutant Trpv4 Recapitulate the Human TRPV4 Disorders. Journal of Bone and Mineral Research. 29(8). 1815–1822. 20 indexed citations

Below, Jennifer E., Dawn Earl, Kathryn M. Shively, et al.. (2012). Whole-Genome Analysis Reveals that Mutations in Inositol Polyphosphate Phosphatase-like 1 Cause Opsismodysplasia. The American Journal of Human Genetics. 92(1). 137–143. 44 indexed citations

Homan, Erica P., Frank Rauch, Ingo Grafe, et al.. (2011). Mutations in SERPINF1 cause osteogenesis imperfecta type VI. Journal of Bone and Mineral Research. 26(12). 2798–2803. 135 indexed citations

Smits, Patrick, Andrew D. Bolton, Vincent Funari, et al.. (2010). Lethal Skeletal Dysplasia in Mice and Humans Lacking the Golgin GMAP-210. New England Journal of Medicine. 362(3). 206–216. 106 indexed citations

10.

Krakow, Deborah, Joris Vriens, Natalia Camacho, et al.. (2009). Mutations in the Gene Encoding the Calcium-Permeable Ion Channel TRPV4 Produce Spondylometaphyseal Dysplasia, Kozlowski Type and Metatropic Dysplasia. The American Journal of Human Genetics. 84(3). 307–315. 148 indexed citations

11.

Tompson, Stuart W., Barry Merriman, Vincent Funari, et al.. (2008). A Recessive Skeletal Dysplasia, SEMD Aggrecan Type, Results from a Missense Mutation Affecting the C-Type Lectin Domain of Aggrecan. The American Journal of Human Genetics. 84(1). 72–79. 101 indexed citations

12.

Rock, Matthew J., Jean Prenen, Vincent Funari, et al.. (2008). Gain-of-function mutations in TRPV4 cause autosomal dominant brachyolmia. Nature Genetics. 40(8). 999–1003. 176 indexed citations

13.

Rimoin, David L., Daniel H. Cohn, Deborah Krakow, et al.. (2007). The Skeletal Dysplasias. Annals of the New York Academy of Sciences. 1117(1). 302–309. 47 indexed citations

14.

Sebald, Eiman, Richard C. Krueger, Lily King, Daniel H. Cohn, & Deborah Krakow. (2003). Isolation of a new member of the ADP-ribosylation like factor gene family, ARL8, from a cartilage cDNA library. Gene. 311. 147–151. 6 indexed citations

15.

Unger, Sheila, Michael D. Briggs, Paul Holden, et al.. (2001). Multiple epiphyseal dysplasia: radiographic abnormalities correlated with genotype. Pediatric Radiology. 31(1). 10–18. 41 indexed citations

16.

Cohn, Daniel H., et al.. (2000). A Locus for an Autosomal Dominant Form of Progressive Renal Failure and Hypertension at Chromosome 1q21. The American Journal of Human Genetics. 67(3). 647–651. 39 indexed citations

17.

Weis, Mary Ann, Douglas J. Wilkin, Hyon J. Kim, et al.. (1998). Structurally Abnormal Type II Collagen in a Severe Form of Kniest Dysplasia Caused by an Exon 24 Skipping Mutation. Journal of Biological Chemistry. 273(8). 4761–4768. 31 indexed citations

18.

Superti‐Furga, Andrea, Johanna Hästbacka, William R. Wilcox, et al.. (1996). Achondrogenesis type IB is caused by mutations in the diastrophic dysplasia sulphate transporter gene. Nature Genetics. 12(1). 100–102. 167 indexed citations

19.

Knowlton, Robert G., Daniel H. Cohn, Michael D. Briggs, et al.. (1995). High-Resolution Genetic and Physical Mapping of Multiple Epiphyseal Dysplasia and Pseudoachondroplasia Mutations at Chromosome 19p13.1-p12. Genomics. 28(3). 513–519. 11 indexed citations

20.

Hecht, Jacqueline T., Clair A. Francomano, Michael D. Briggs, et al.. (1993). Linkage of typical pseudoachondroplasia to chromosome 19. Genomics. 18(3). 661–666. 43 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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