Daniel H Cohn

9PUBLICATIONS
12CO-AUTHORS
Medical infection agents (incl. prions)Gene expression (incl. microarray and other genome-wide approaches)Cancer therapy (excl. chemotherapy and radiation therapy)Developmental genetics (incl. sex determination)Genome structure and regulation
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Publications (9)

|Jul 06, 2026
Biallelic Variants in MIMS1 Produce a Form of Spondyloepimetaphyseal Dysplasia With Tracheal Stenosis and Ectodermal Dysplasia (SEMDTSED).

|Feb 13, 2023
Nosology of genetic skeletal disorders: 2023 revision.

Sheila Unger, Carlos R Ferreira, Geert R Mortier

|Oct 22, 2019
Nosology and classification of genetic skeletal disorders: 2019 revision.

Geert R Mortier, Daniel H Cohn, Valerie Cormier-Daire

|Aug 08, 2019
Dominant-negative SOX9 mutations in campomelic dysplasia.

Fabiana Csukasi, Ivan Duran, Wenjuan Zhang

|Nov 20, 2018
Autosomal recessive Stickler syndrome resulting from a COL9A3 mutation.

Andrea Hanson-Kahn, Bing Li, Daniel H Cohn

|Dec 22, 2017
Genes uniquely expressed in human growth plate chondrocytes uncover a distinct regulatory network.

Bing Li, Karthika Balasubramanian, Deborah Krakow

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Frequent Collaborators

2 joint publications

Deborah Krakow

2 joint publications

Stephen Robertson

1 joint publications

Andrea Hanson-Kahn

1 joint publications

Ivan Duran