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)Solid mechanicsDevelopmental genetics (incl. sex determination)

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Publications (9)

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|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

|Jun 05, 2019

The α2 chain of type IX collagen is essential for type IX collagen biosynthesis.

Karthika Balasubramanian, MaryAnn Weis, David R Eyre

|Nov 20, 2018

Autosomal recessive Stickler syndrome resulting from a COL9A3 mutation.

Andrea Hanson-Kahn, Bing Li, Daniel H Cohn

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Frequent Collaborators

Deborah Krakow

Stephen Robertson

Andrea Hanson-Kahn

Ivan Duran

Fabiana Csukasi

Geert R Mortier

Débora R Bertola

Katta M Girisha

Outi Makitie

Andrea Superti-Furga

Frequent Collaborators

Deborah Krakow

Stephen Robertson

Andrea Hanson-Kahn

Ivan Duran