David L. Rimoin

Por Cohn, Daniel H., Shapiro, Larry J., Kaback, Michael M.
Publicado em 2012

Reasons for Non-Disclosure of Sexual Orientation among Behaviorally-Bisexual Men: Non-disclosure as Stigma Management

Por Schrimshaw, Eric W., Downing, Martin J., Cohn, Daniel J.
Publicado no Arch Sex Behav (2016)

Genes uniquely expressed in human growth plate chondrocytes uncover a distinct regulatory network

Por Li, Bing, Balasubramanian, Karthika, Krakow, Deborah, Cohn, Daniel H.
Publicado no BMC Genomics (2017)

Engineering of bio-hybrid materials by electrospinning polymer-microbe fibers

Por Liu, Ying, Rafailovich, Miriam H., Malal, Ram, Cohn, Daniel, Chidambaram, Dev
Publicado em 2009

Cartilage oligomeric matrix protein promotes cell attachment via two independent mechanisms involving CD47 and αVβ3 integrin

Por Rock, Matthew J., Holden, Paul, Horton, William A., Cohn, Daniel H.
Publicado em 2009

Conceptions of Privacy and the Non-disclosure of Same-Sex Behaviour Among Behaviourally-Bisexual Men in Heterosexual Relationships

Por Schrimshaw, Eric W., Downing, Martin J., Cohn, Daniel J., Siegel, Karolynn
Publicado em 2014

Mice Expressing Mutant Trpv4 Recapitulate the Human TRPV4 Disorders()

Por Weinstein, Michael M., Tompson, Stuart W., Chen, Yuqing, Lee, Brendan, Cohn, Daniel H.
Publicado em 2014

Peptidyl 3-Hydroxyproline-Binding Properties of Type I Collagen Suggest a Function in Fibril Supramolecular Assembly

Por Hudson, David M., Kim, Lammy S., Weis, MaryAnn, Cohn, Daniel H., Eyre, David R.
Publicado em 2012

A Second Locus for Schneckenbecken Dysplasia Identified by a Mutation in the Gene Encoding Inositol Polyphosphate Phosphatase-Like 1 (INPPL1)

Por Lee, Hane, Nevarez, Lisette, Lachman, Ralph S., Wilcox, William R., Krakow, Deborah, Cohn, Daniel H.
Publicado no Am J Med Genet A (2015)

A Locus for an Autosomal Dominant Form of Progressive Renal Failure and Hypertension at Chromosome 1q21

Por Cohn, Daniel H., Shohat, Tamy, Yahav, Michal, Ilan, Tsafra, Rechavi, Gidi, King, Lily, Shohat, Mordechai
Publicado em 2000

Autosomal recessive Stickler syndrome resulting from a COL9A3 mutation

Por Hanson-Kahn, Andrea, Li, Bing, Cohn, Daniel H., Nickerson, Deborah A., Bamshad, Michael J., Hudgins, Louanne
Publicado no Am J Med Genet A (2018)

Somatic Mosaicism for a Lethal TRPV4 Mutation Results in Non-Lethal Metatropic Dysplasia

Por Weinstein, Michael M., Kang, Taekyu, Lachman, Ralph S., Bamshad, Michael, Nickerson, Deborah A., Krakow, Deborah, Cohn, Daniel H.
Publicado no Am J Med Genet A (2016)

Cartilage-selective genes identified in genome-scale analysis of non-cartilage and cartilage gene expression

Por Funari, Vincent A, Day, Allen, Krakow, Deborah, Cohn, Zachary A, Chen, Zugen, Nelson, Stanley F, Cohn, Daniel H
Publicado em 2007

IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome

Por Zhang, Wenjuan, Taylor, S. Paige, Nevarez, Lisette, Lachman, Ralph S., Nickerson, Deborah A., Bamshad, Michael, Krakow, Deborah, Cohn, Daniel H.
Publicado no Hum Mol Genet (2016)

Mental Retardation and Abnormal Skeletal Development (Dyggve-Melchior-Clausen Dysplasia) Due to Mutations in a Novel, Evolutionarily Conserved Gene

Por Cohn, Daniel H., Ehtesham, Nadia, Krakow, Deborah, Unger, Sheila, Shanske, Alan, Reinker, Kent, Powell, Berkley R., Rimoin, David L.
Publicado em 2003

Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis

Por Marques, Felipe, Tenney, Jessica, Duran, Ivan, Martin, Jorge, Nevarez, Lisette, Pogue, Robert, Krakow, Deborah, Cohn, Daniel H., Li, Bing
Publicado no PLoS Genet (2016)

Correction: Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis

Por Marques, Felipe, Tenney, Jessica, Duran, Ivan, Martin, Jorge, Nevarez, Lisette, Pogue, Robert, Krakow, Deborah, Cohn, Daniel H., Li, Bing
Publicado no PLoS Genet (2016)

Prevalence of Trachoma in Senegal: Results of Baseline Surveys in 17 Districts

Por Sarr, Boubacar, Sissoko, Mactar, Fall, Mawo, Nizigama, Lionel, Cohn, Daniel, Willis, Rebecca, Fuller, Brian, O’Neil, Maggie, Solomon, Anthony W
Publicado no Ophthalmic Epidemiol (2018)

Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome

Por Farrington-Rock, Claire, Kirilova, Veneta, Dillard-Telm, Lisa, Borowsky, Alexander D., Chalk, Sara, Rock, Matthew J., Cohn, Daniel H., Krakow, Deborah
Publicado em 2007

Improving the efficiency of genomic loci capture using oligonucleotide arrays for high throughput resequencing

Por Lee, Hane, O'Connor, Brian D, Merriman, Barry, Funari, Vincent A, Homer, Nils, Chen, Zugen, Cohn, Daniel H, Nelson, Stanley F
Publicado em 2009