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Deb Krakow, M.D.
Contact Information:
Fax Number:
310-825-5409
Lab Number:
310-983-3049
Office Phone Number:
310-983-1252
Work Address:
UCLA Ortho Surg 615 Charles E. Young Dr. So, Rm 410 BOX 957358 Los Angeles, CA 90095 UNITED STATES
Associate Professor,
Obstetrics and Gynecology
Orthopaedic Surgery
Human Genetics
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Member,
ACCESS Program: Dept. of Human Genetics
Genetics
CTSI
Research Education, Training, and Career Development Program (CTSI-ED)
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A Short Biography:
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
Awards and Honors:
Cedars-Sinai Medical Center, Los Angeles, California
Harbor-UCLA Medical Center, Torrance, CA
UCLA Intercampus Medical Genetics Training Program, Los Angeles, CA
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.
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 sequencing.
American journal of human genetics,
2010; 87(4):
532-7.
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 gene.
American 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, 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, 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.
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.
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