Deborah Krakow, MD

Dr. Krakow received her bachelor’s degree from Arizona State University in Tempe and her medical degree from Chicago Medical School. After an internship and residency in obstetrics and gynecology at Cedars-Sinai Medical Center, she completed fellowships in maternal-fetal medicine at Harbor-UCLA Medical Center and in research and clinical genetics at the UCLA Intercampus Medical Genetics Training Program.

Work Titles/Affiliations

• Professor and Chair, Obstetrics and Gynecology
• Professor, Orthopedic Surgery, Human Genetics

Publications

• Merrill Amy E, Sarukhanov Anna, Krejci Pavel, Idoni Brian, Camacho Natalia, Estrada Kristine D, Lyons Karen M, Deixler Hannah, Robinson Haynes, Chitayat David, Curry Cynthia J, Lachman Ralph S, Wilcox William R, Krakow Deborah   Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling American journal of human genetics, 2012; 90(3): 550-7. 
• Tompson Stuart W, Faqeih Eissa Ali, Ala-Kokko Leena, Hecht Jacqueline T, Miki Rika, Funari Tara, Funari Vincent A, Nevarez Lisette, Krakow Deborah, Cohn Daniel H   Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2 American journal of medical genetics. Part A, 2012; 158A(2): 309-14. 
• Lee Hane, Graham John M, Rimoin David L, Lachman Ralph S, Krejci Pavel, Tompson Stuart W, Nelson Stanley F, Krakow Deborah, Cohn Daniel H   Exome sequencing identifies PDE4D mutations in acrodysostosis American journal of human genetics, 2012; 90(4): 746-51. 
• Nemec Stefan F, Cohn Daniel H, Krakow Deborah, Funari Vincent A, Rimoin David L, Lachman Ralph S   The importance of conventional radiography in the mutational analysis of skeletal dysplasias (the TRPV4 mutational family) Pediatric radiology, 2012; 42(1): 15-23. 
• Funari Vincent A, Krakow Deborah, Nevarez Lisette, Chen Zugen, Funari Tara L, Vatanavicharn Nithiwat, Wilcox William R, Rimoin David L, Nelson Stanley F, Cohn Daniel H   BMPER mutation in diaphanospondylodysostosis identified by ancestral autozygosity mapping and targeted high-throughput sequencingAmerican journal of human genetics, 2010; 87(4): 532-7. 
• Camacho Natalia, Krakow Deborah, Johnykutty Sharlin, Katzman Philip J, Pepkowitz Samuel, Vriens Joris, Nilius Bernd, Boyce Brendan F, Cohn Daniel H  Dominant TRPV4 mutations in nonlethal and lethal metatropic dysplasia American journal of medical genetics. Part A, 2010; 152A(5): 1169-77. 
• Tompson Stuart W, Bacino Carlos A, Safina Nicole P, Bober Michael B, Proud Virginia K, Funari Tara, Wangler Michael F, Nevarez Lisette, Ala-Kokko Leena, Wilcox William R, Eyre David R, Krakow Deborah, Cohn Daniel H   Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen geneAmerican journal of human genetics, 2010; 87(5): 708-12. 
• Krakow Deborah, Rimoin David L   The skeletal dysplasias Genetics in medicine : official journal of the American College of Medical Genetics, 2010; 12(6): 327-41. 
• Merrill Amy E, Merriman Barry, Farrington-Rock Claire, Camacho Natalia, Sebald Eiman T, Funari Vincent A, Schibler Matthew J, Firestein Marc H, Cohn Zachary A, Priore Mary Ann, Thompson Alicia K, Rimoin David L, Nelson Stanley F, Cohn Daniel H, Krakow Deborah   Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome American journal of human genetics, 2009; 84(4): 542-9. 
• Krakow Deborah, Lachman Ralph S, Rimoin David L   Guidelines for the prenatal diagnosis of fetal skeletal dysplasias Genetics in medicine : official journal of the American College of Medical Genetics, 2009; 11(2): 127-33. 
• Krakow Deborah, Vriens Joris, Camacho Natalia, Luong Phi, Deixler Hannah, Funari Tara L, Bacino Carlos A, Irons Mira B, Holm Ingrid A, Sadler Laurie, Okenfuss Ericka B, Janssens Annelies, Voets Thomas, Rimoin David L, Lachman Ralph S, Nilius Bernd, Cohn Daniel H   Mutations in the gene encoding the calcium-permeable ion channel TRPV4 produce spondylometaphyseal dysplasia, Kozlowski type and metatropic dysplasia American journal of human genetics, 2009; 84(3): 307-15. 
• Farrington-Rock Claire, Kirilova Veneta, Dillard-Telm Lisa, Borowsky Alexander D, Chalk Sara, Rock Matthew J, Cohn Daniel H, Krakow Deborah   Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome Human molecular genetics, 2008; 17(5): 631-41. 
• Krakow Deborah, Alanay Yasemin, Rimoin Lauren P, Lin Victoria, Wilcox William R, Lachman Ralph S, Rimoin David L   Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: a retrospective and prospective analysis American journal of medical genetics. Part A, 2008; 146A(15): 1917-24. 
• Brunetti-Pierri Nicola, Esposito Valentina, De Brasi Daniele, Mattiacci Dario Maria, Krakow Deborah, Lee Brendan, Salerno Mariacarolina  Spondylocarpotarsal synostosis: long-term follow-up of a case due to FLNB mutations American journal of medical genetics. Part A, 2008; 146A(9): 1230-3. 
• Alanay Yasemin, Krakow Deborah, Rimoin David L, Lachman Ralph S   Angulated femurs and the skeletal dysplasias: experience of the International Skeletal Dysplasia Registry (1988-2006) American journal of medical genetics. Part A, 2007; 143A(11): 1159-68. 
• Funari Vincent A, Day Allen, Krakow Deborah, Cohn Zachary A, Chen Zugen, Nelson Stanley F, Cohn Daniel H   Cartilage-selective genes identified in genome-scale analysis of non-cartilage and cartilage gene expression BMC genomics, 2007; 8(4): 165. 
• Krejci Pavel, Krakow Deborah, Mekikian Pertchoui B, Wilcox William R   Fibroblast growth factors 1, 2, 17, and 19 are the predominant FGF ligands expressed in human fetal growth plate cartilage Pediatric research, 2007; 61(3): 267-72. 
• Miller Michelle, Krakow Deborah, Pepkowitz Samuel   Polyvalvular disease in a fetus with normal chromosomes Congenital heart disease, 2007; 2(3): 214-7. 
• Rimoin David L, Cohn Daniel, Krakow Deborah, Wilcox William, Lachman Ralph S, Alanay Yasemin   The skeletal dysplasias: clinical-molecular correlationsAnnals of the New York Academy of Sciences, 2007; 1117(6): 302-9. 
• Farrington-Rock Claire, Firestein Marc H, Bicknell Louise S, Superti-Furga Andrea, Bacino Carlos A, Cormier-Daire Valerie, Le Merrer Martine, Baumann Clarisse, Roume Joelle, Rump Patrick, Verheij Joke B G M, Sweeney Elizabeth, Rimoin David L, Lachman Ralph S, Robertson Stephen P, Cohn Daniel H, Krakow Deborah   Mutations in two regions of FLNB result in atelosteogenesis I and III Human mutation, 2006; 27(7): 705-10. 
• Steiner C, Ehtesham N, Taylor K D, Sebald E, Cantor R, King L M, Guo X, Hang T, Hu M S, Cui J-R, Friedman B, Norato D, Allanson J, Honeywell C, Mettler G, Field F, Lachman R, Cohn D H, Krakow D   A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14 Journal of medical genetics, 2004; 41(4): 266-9. 
• Pogue Robert, Sebald Eiman, King Lily, Kronstadt Erik, Krakow Deborah, Cohn Daniel H   A transcriptional profile of human fetal cartilage Matrix biology : journal of the International Society for Matrix Biology, 2004; 23(5): 299-307. 
• Krakow Deborah, Robertson Stephen P, King Lily M, Morgan Timothy, Sebald Eiman T, Bertolotto Cristina, Wachsmann-Hogiu Sebastian, Acuna Dora, Shapiro Sandor S, Takafuta Toshiro, Aftimos Salim, Kim Chong Ae, Firth Helen, Steiner Carlos E, Cormier-Daire Valerie, Superti-Furga Andrea, Bonafe Luisa, Graham John M, Grix Arthur, Bacino Carlos A, Allanson Judith, Bialer Martin G, Lachman Ralph S, Rimoin David L, Cohn Daniel H   Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis Nature genetics, 2004; 36(4): 405-10. 
• Krakow Deborah, Sebald Eiman T, Pogue Robert, Rimoin Lauren P, King Lily, Cohn Daniel H   Analysis of clones from a human cartilage cDNA library provides insight into chondrocyte gene expression and identifies novel candidate genes for the osteochondrodysplasias Molecular genetics and metabolism, 2003; 79(1): 34-42. 
• Sebald Eiman, Krueger Richard, King Lily M, Cohn Daniel H, Krakow Deborah   Isolation of a new member of the ADP-ribosylation like factor gene family, ARL8, from a cartilage cDNA library Gene, 2003; 311(5): 147-51. 
• Cohn Daniel H, Ehtesham Nadia, Krakow Deborah, Unger Sheila, Shanske Alan, Reinker Kent, Powell Berkley R, Rimoin David L   Mental retardation and abnormal skeletal development (Dyggve-Melchior-Clausen dysplasia) due to mutations in a novel, evolutionarily conserved gene American journal of human genetics, 2003; 72(2): 419-28.