Deborah Krakow

Nosology and classification of genetic skeletal disorders: 2019 revision

Geert Mortier, Daniel H. Cohn, Valérie Cormier‐Daire et al. · American Journal of Medical Genetics Part A · 2019 · 592 citations

Dominance of SOX9 function over RUNX2 during skeletogenesis

Guang Zhou, Qiping Zheng, Feyza Engin et al. · Proceedings of the National Academy of Sciences · 2006 · 370 citations · Full text

Runx Gene Family, Sox9 Function, Sclerostin +20

Human Ehlers-Danlos Syndrome Type VII C and Bovine Dermatosparaxis Are Caused by Mutations in the Procollagen I N-Proteinase Gene

Alain Colige, Aleksander L. Sieroń, Shi-Wu Li et al. · The American Journal of Human Genetics · 1999 · 362 citations · Full text

Autoimmune Disease, Disease Mechanism, Genetic Disorder +11

<i>WNT1</i> Mutations in Early-Onset Osteoporosis and Osteogenesis Imperfecta

Christine Lainé, Kyu Sang Joeng, Philippe M. Campeau et al. · New England Journal of Medicine · 2013 · 347 citations · Full text

Bone Disease, Early-onset Osteoporosis, Developmental Biology +11

Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis

Yaoqin Gong, Deborah Krakow, José Roberto Marcelino et al. · Nature Genetics · 1999 · 346 citations

Developmental Biology, Genetic Disorder, Developmental Genetics +7