Loading...

Deborah Krakow

Title(s)Professor, Orthopaedic Surgery
SchoolMedicine
Address760 Westwood Plaza 410E
Los Angeles CA 90024
Phone3107942699
vCardDownload vCard
    Other Positions
    Title(s)Professor, Human Genetics

    Title(s)Professor, Obstetrics and Gynecology

    Title(s)Professor, Pediatrics


    Collapse Research 
    Collapse Research Activities and Funding
    Unraveling the mechanisms of prenatal-onset disorders affecting the skeleton
    NIH/NIAMS R01AR066124Apr 1, 2014 - Mar 31, 2019
    Role: Principal Investigator
    Short-rib polydactyly and the skeletal ciliopathies
    NIH/NIDCR R01DE019567Dec 1, 2008 - Mar 31, 2014
    Role: Co-Principal Investigator
    MOLECULAR GENETICS OF FACIO AUDIO SYMPHALANGISM
    NIH/NICHD K08HD001205Sep 1, 1997 - Aug 31, 2001
    Role: Principal Investigator

    Collapse ORNG Applications 
    Collapse Clinical Trials

    Collapse Bibliographic 
    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
    Newest   |   Oldest   |   Most Cited   |   Most Discussed   |   Timeline   |   Field Summary   |   Plain Text
    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Improvement in ventriculomegaly following cervicomedullary decompressive surgery in children with achondroplasia and foramen magnum stenosis. Am J Med Genet A. 2020 Jun 11. Kashanian A, Chan J, Mukherjee D, Pressman BD, Krakow D, Danielpour M. PMID: 32525257.
      View in: PubMed   Mentions:    Fields:    
    2. Fetal cardiac rhabdomyomas treated with maternal sirolimus. Prenat Diagn. 2020 02; 40(3):358-364. Pluym ID, Sklansky M, Wu JY, Afshar Y, Holliman K, Devore GR, Walden A, Platt LD, Krakow D. PMID: 31742705.
      View in: PubMed   Mentions:    Fields:    
    3. Nosology and classification of genetic skeletal disorders: 2019 revision. Am J Med Genet A. 2019 12; 179(12):2393-2419. Mortier GR, Cohn DH, Cormier-Daire V, Hall C, Krakow D, Mundlos S, Nishimura G, Robertson S, Sangiorgi L, Savarirayan R, Sillence D, Superti-Furga A, Unger S, Warman ML. PMID: 31633310.
      View in: PubMed   Mentions: 11     Fields:    
    4. Diagnostic utility of transcriptome sequencing for rare Mendelian diseases. Genet Med. 2020 Mar; 22(3):490-499. Lee H, Huang AY, Wang LK, Yoon AJ, Renteria G, Eskin A, Signer RH, Dorrani N, Nieves-Rodriguez S, Wan J, Douine ED, Woods JD, Dell'Angelica EC, Fogel BL, Martin MG, Butte MJ, Parker NH, Wang RT, Shieh PB, Wong DA, Gallant N, Singh KE, Tavyev Asher YJ, Sinsheimer JS, Krakow D, Loo SK, Allard P, Papp JC, Palmer CGS, Martinez-Agosto JA, Nelson SF. PMID: 31607746.
      View in: PubMed   Mentions: 6     Fields:    
    5. Dominant-negative SOX9 mutations in campomelic dysplasia. Hum Mutat. 2019 12; 40(12):2344-2352. Csukasi F, Duran I, Zhang W, Martin JH, Barad M, Bamshad M, Weis MA, Eyre D, Krakow D, Cohn DH. PMID: 31389106.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    6. The a2 chain of type IX collagen is essential for type IX collagen biosynthesis. Am J Med Genet A. 2019 08; 179(8):1672-1677. Balasubramanian K, Weis M, Eyre DR, Martin J, Ortiz-Sanchez J, Duran I, Vangala S, Wang J, Friedman RA, Krakow D, Cohn DH. PMID: 31161720.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimals
    7. Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes. Am J Hum Genet. 2019 03 07; 104(3):422-438. Burrage LC, Reynolds JJ, Baratang NV, Phillips JB, Wegner J, McFarquhar A, Higgs MR, Christiansen AE, Lanza DG, Seavitt JR, Jain M, Li X, Parry DA, Raman V, Chitayat D, Chinn IK, Bertuch AA, Karaviti L, Schlesinger AE, Earl D, Bamshad M, Savarirayan R, Doddapaneni H, Muzny D, Jhangiani SN, Eng CM, Gibbs RA, Bi W, Emrick L, Rosenfeld JA, Postlethwait J, Westerfield M, Dickinson ME, Beaudet AL, Ranza E, Huber C, Cormier-Daire V, Shen W, Mao R, Heaney JD, Orange JS, Bertola D, Yamamoto GL, Baratela WAR, Butler MG, Ali A, Adeli M, Cohn DH, Krakow D, Jackson AP, Lees M, Offiah AC, Carlston CM, Carey JC, Stewart GS, Bacino CA, Campeau PM, Lee B. PMID: 30773277.
      View in: PubMed   Mentions:    Fields:    Translation:HumansAnimalsCells
    8. A new biometric: In utero growth curves for metacarpal and phalangeal lengths reveal an embryonic patterning ratio. Prenat Diagn. 2019 02; 39(3):200-208. Rao R, Gornbein J, Afshar Y, Platt LD, DeVore GR, Krakow D. PMID: 30488473.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    9. First-Trimester Abdominal Circumference (Versus Crown Rump Length) Improves Precision in Inter- and Intraobserver Variability. J Ultrasound Med. 2019 Aug; 38(8):2161-2167. Afshar Y, Gutkin R, Krakow D, Cuckle H, Silverman NS, Platt LD. PMID: 30593696.
      View in: PubMed   Mentions:    Fields:    Translation:Humans
    10. The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling. Sci Transl Med. 2018 09 19; 10(459). Csukasi F, Duran I, Barad M, Barta T, Gudernova I, Trantirek L, Martin JH, Kuo CY, Woods J, Lee H, Cohn DH, Krejci P, Krakow D. PMID: 30232230.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    11. NRP1 haploinsufficiency predisposes to the development of Tetralogy of Fallot. Am J Med Genet A. 2018 03; 176(3):649-656. Duran I, Tenney J, Warren CM, Sarukhanov A, Csukasi F, Skalansky M, Iruela-Arispe ML, Krakow D. PMID: 29363855.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    12. Genes uniquely expressed in human growth plate chondrocytes uncover a distinct regulatory network. BMC Genomics. 2017 Dec 20; 18(1):983. Li B, Balasubramanian K, Krakow D, Cohn DH. PMID: 29262782.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    13. Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies. Hum Mutat. 2018 01; 39(1):152-166. Zhang W, Taylor SP, Ennis HA, Forlenza KN, Duran I, Li B, Sanchez JAO, Nevarez L, Nickerson DA, Bamshad M, Lachman RS, Krakow D, Cohn DH. PMID: 29068549.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    14. Mutations in Fibronectin Cause a Subtype of Spondylometaphyseal Dysplasia with "Corner Fractures". Am J Hum Genet. 2017 Nov 02; 101(5):815-823. Lee CS, Fu H, Baratang N, Rousseau J, Kumra H, Sutton VR, Niceta M, Ciolfi A, Yamamoto G, Bertola D, Marcelis CL, Lugtenberg D, Bartuli A, Kim C, Hoover-Fong J, Sobreira N, Pauli R, Bacino C, Krakow D, Parboosingh J, Yap P, Kariminejad A, McDonald MT, Aracena MI, Lausch E, Unger S, Superti-Furga A, Lu JT, Cohn DH, Tartaglia M, Lee BH, Reinhardt DP, Campeau PM. PMID: 29100092.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    15. MED resulting from recessively inherited mutations in the gene encoding calcium-activated nucleotidase CANT1. Am J Med Genet A. 2017 Sep; 173(9):2415-2421. Balasubramanian K, Li B, Krakow D, Nevarez L, Ho PJ, Ainsworth JA, Nickerson DA, Bamshad MJ, Immken L, Lachman RS, Cohn DH. PMID: 28742282.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    16. Autosomal dominant frontometaphyseal dysplasia: Delineation of the clinical phenotype. Am J Med Genet A. 2017 Jul; 173(7):1739-1746. Wade EM, Jenkins ZA, Daniel PB, Morgan T, Addor MC, Adés LC, Bertola D, Bohring A, Carter E, Cho TJ, de Geus CM, Duba HC, Fletcher E, Hadzsiev K, Hennekam RCM, Kim CA, Krakow D, Morava E, Neuhann T, Sillence D, Superti-Furga A, Veenstra-Knol HE, Wieczorek D, Wilson LC, Markie DM, Robertson SP. PMID: 28498505.
      View in: PubMed   Mentions: 2     Fields:    
    17. Mutations in IFT-A satellite core component genes IFT43 and IFT121 produce short rib polydactyly syndrome with distinctive campomelia. Cilia. 2017; 6:7. Duran I, Taylor SP, Zhang W, Martin J, Qureshi F, Jacques SM, Wallerstein R, Lachman RS, Nickerson DA, Bamshad M, Cohn DH, Krakow D. PMID: 28400947.
      View in: PubMed   Mentions:
    18. A Chaperone Complex Formed by HSP47, FKBP65, and BiP Modulates Telopeptide Lysyl Hydroxylation of Type I Procollagen. J Bone Miner Res. 2017 Jun; 32(6):1309-1319. Duran I, Martin JH, Weis MA, Krejci P, Konik P, Li B, Alanay Y, Lietman C, Lee B, Eyre D, Cohn DH, Krakow D. PMID: 28177155.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimalsCells
    19. A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFß signaling and cause autosomal dominant spondylocarpotarsal synostosis. Sci Rep. 2017 02 16; 7:41803. Zieba J, Zhang W, Chong JX, Forlenza KN, Martin JH, Heard K, Grange DK, Butler MG, Kleefstra T, Lachman RS, Nickerson D, Regnier M, Cohn DH, Bamshad M, Krakow D. PMID: 28205584.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    20. Correction: Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis. PLoS Genet. 2016 Dec; 12(12):e1006502. Marques F, Tenney J, Duran I, Martin J, Nevarez L, Pogue R, Krakow D, Cohn DH, Li B. PMID: 27935951.
      View in: PubMed   Mentions:    Fields:    
    21. Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome. Sci Rep. 2016 Sep 26; 6:34232. Duran I, Taylor SP, Zhang W, Martin J, Forlenza KN, Spiro RP, Nickerson DA, Bamshad M, Cohn DH, Krakow D. PMID: 27666822.
      View in: PubMed   Mentions: 8     Fields:    
    22. Altered mRNA Splicing, Chondrocyte Gene Expression and Abnormal Skeletal Development due to SF3B4 Mutations in Rodriguez Acrofacial Dysostosis. PLoS Genet. 2016 09; 12(9):e1006307. Marques F, Tenney J, Duran I, Martin J, Nevarez L, Pogue R, Krakow D, Cohn DH, Li B. PMID: 27622494.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    23. Somatic mosaicism for a lethal TRPV4 mutation results in non-lethal metatropic dysplasia. Am J Med Genet A. 2016 12; 170(12):3298-3302. Weinstein MM, Kang T, Lachman RS, Bamshad M, Nickerson DA, Krakow D, Cohn DH. PMID: 27530454.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    24. An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndrome. Hum Mol Genet. 2016 09 15; 25(18):3998-4011. Paige Taylor S, Kunova Bosakova M, Varecha M, Balek L, Barta T, Trantirek L, Jelinkova I, Duran I, Vesela I, Forlenza KN, Martin JH, Hampl A, Bamshad M, Nickerson D, Jaworski ML, Song J, Ko HW, Cohn DH, Krakow D, Krejci P. PMID: 27466187.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    25. IFT52 mutations destabilize anterograde complex assembly, disrupt ciliogenesis and result in short rib polydactyly syndrome. Hum Mol Genet. 2016 09 15; 25(18):4012-4020. Zhang W, Taylor SP, Nevarez L, Lachman RS, Nickerson DA, Bamshad M, Krakow D, Cohn DH. PMID: 27466190.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    26. Corrigendum: The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery. Nat Genet. 2016 07 27; 48(8):970. Toriyama M, Lee C, Taylor SP, Duran I, Cohn DH, Bruel AL, Tabler JM, Drew K, Kelly MR, Kim S, Park TJ, Braun DA, Pierquin G, Biver A, Wagner K, Malfroot A, Panigrahi I, Franco B, Al-Lami HA, Yeung Y, Choi YJ, Duffourd Y, Faivre L, Rivière JB, Chen J, Liu KJ, Marcotte EM, Hildebrandt F, Thauvin-Robinet C, Krakow D, Jackson PK, Wallingford JB. PMID: 27463398.
      View in: PubMed   Mentions: 1     Fields:    
    27. Clinical and radiographic delineation of Bent Bone Dysplasia-FGFR2 type or Bent Bone Dysplasia with Distinctive Clavicles and Angel-shaped Phalanges. Am J Med Genet A. 2016 10; 170(10):2652-61. Krakow D, Cohn DH, Wilcox WR, Noh GJ, Raffel LJ, Sarukhanov A, Ivanova MH, Danielpour M, Grange DK, Elliott AM, Bernstein JA, Rimoin DL, Merrill AE, Lachman RS. PMID: 27240702.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    28. The ciliopathy-associated CPLANE proteins direct basal body recruitment of intraflagellar transport machinery. Nat Genet. 2016 06; 48(6):648-56. Toriyama M, Lee C, Taylor SP, Duran I, Cohn DH, Bruel AL, Tabler JM, Drew K, Kelly MR, Kim S, Park TJ, Braun DA, Pierquin G, Biver A, Wagner K, Malfroot A, Panigrahi I, Franco B, Al-Lami HA, Yeung Y, Choi YJ, Duffourd Y, Faivre L, Rivière JB, Chen J, Liu KJ, Marcotte EM, Hildebrandt F, Thauvin-Robinet C, Krakow D, Jackson PK, Wallingford JB. PMID: 27158779.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansAnimalsCells
    29. TGFß and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions. PLoS Genet. 2016 Mar; 12(3):e1005936. Zieba J, Forlenza KN, Khatra JS, Sarukhanov A, Duran I, Rigueur D, Lyons KM, Cohn DH, Merrill AE, Krakow D. PMID: 27019229.
      View in: PubMed   Mentions: 9     Fields:    Translation:HumansAnimalsCells
    30. Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndrome. Nat Commun. 2015 Jun 16; 6:7092. Taylor SP, Dantas TJ, Duran I, Wu S, Lachman RS, Nelson SF, Cohn DH, Vallee RB, Krakow D. PMID: 26077881.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansCells
    31. Detection of Y chromosome material in a 46,XX male with SRY translocation: novel application of cell-free fetal DNA testing. Prenat Diagn. 2015 Aug; 35(8):823-5. Benedict K, Han CS, Silverman NS, Krakow D, Platt LD. PMID: 25871731.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    32. A second locus for Schneckenbecken dysplasia identified by a mutation in the gene encoding inositol polyphosphate phosphatase-like 1 (INPPL1). Am J Med Genet A. 2015 Oct; 167A(10):2470-3. Lee H, Nevarez L, Lachman RS, Wilcox WR, Krakow D, Cohn DH. PMID: 25997753.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    33. Skeletal dysplasias. Clin Perinatol. 2015 Jun; 42(2):301-19, viii. Krakow D. PMID: 26042906.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    34. HSP47 and FKBP65 cooperate in the synthesis of type I procollagen. Hum Mol Genet. 2015 Apr 01; 24(7):1918-28. Duran I, Nevarez L, Sarukhanov A, Wu S, Lee K, Krejci P, Weis M, Eyre D, Krakow D, Cohn DH. PMID: 25510505.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    35. Prenatal and postnatal findings in serpentine fibula polycystic kidney syndrome and a review of the NOTCH2 spectrum disorders. Am J Med Genet A. 2014 Oct; 164A(10):2490-5. Martin BM, Ivanova MH, Sarukhanov A, Kim A, Power P, Pugash D, Popescu OE, Lachman RS, Krakow D, Patel MS. PMID: 24995648.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    36. Dynamic cervicomedullary cord compression and alterations in cerebrospinal fluid dynamics in children with achondroplasia: review of an 11-year surgical case series. J Neurosurg Pediatr. 2014 Sep; 14(3):238-44. Mukherjee D, Pressman BD, Krakow D, Rimoin DL, Danielpour M. PMID: 24971605.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    37. Opsismodysplasia resulting from an insertion mutation in the SH2 domain, which destabilizes INPPL1. Am J Med Genet A. 2014 Sep; 164A(9):2407-11. Li B, Krakow D, Nickerson DA, Bamshad MJ, Chang Y, Lachman RS, Yilmaz A, Kayserili H, Cohn DH. PMID: 24953221.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    38. Bent bone dysplasia syndrome reveals nucleolar activity for FGFR2 in ribosomal DNA transcription. Hum Mol Genet. 2014 Nov 01; 23(21):5659-71. Neben CL, Idoni B, Salva JE, Tuzon CT, Rice JC, Krakow D, Merrill AE. PMID: 24908667.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansAnimalsCells
    39. Patient-derived skeletal dysplasia induced pluripotent stem cells display abnormal chondrogenic marker expression and regulation by BMP2 and TGFß1. Stem Cells Dev. 2014 Jul 01; 23(13):1464-78. Saitta B, Passarini J, Sareen D, Ornelas L, Sahabian A, Argade S, Krakow D, Cohn DH, Svendsen CN, Rimoin DL. PMID: 24559391.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    40. Routine measurement of amniotic fluid alpha-fetoprotein and acetylcholinesterase: the need for a reevaluation. Am J Obstet Gynecol. 2014 Aug; 211(2):139.e1-6. Flick A, Krakow D, Martirosian A, Silverman N, Platt LD. PMID: 24530818.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    41. WDR34 mutations that cause short-rib polydactyly syndrome type III/severe asphyxiating thoracic dysplasia reveal a role for the NF-?B pathway in cilia. Am J Hum Genet. 2013 Nov 07; 93(5):926-31. Huber C, Wu S, Kim AS, Sigaudy S, Sarukhanov A, Serre V, Baujat G, Le Quan Sang KH, Rimoin DL, Cohn DH, Munnich A, Krakow D, Cormier-Daire V. PMID: 24183449.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCells
    42. WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta. N Engl J Med. 2013 May 09; 368(19):1809-16. Laine CM, Joeng KS, Campeau PM, Kiviranta R, Tarkkonen K, Grover M, Lu JT, Pekkinen M, Wessman M, Heino TJ, Nieminen-Pihala V, Aronen M, Laine T, Kröger H, Cole WG, Lehesjoki AE, Nevarez L, Krakow D, Curry CJ, Cohn DH, Gibbs RA, Lee BH, Mäkitie O. PMID: 23656646.
      View in: PubMed   Mentions: 85     Fields:    Translation:HumansAnimals
    43. Whole-genome analysis reveals that mutations in inositol polyphosphate phosphatase-like 1 cause opsismodysplasia. Am J Hum Genet. 2013 Jan 10; 92(1):137-43. Below JE, Earl DL, Shively KM, McMillin MJ, Smith JD, Turner EH, Stephan MJ, Al-Gazali LI, Hertecant JL, Chitayat D, Unger S, Cohn DH, Krakow D, Swanson JM, Faustman EM, Shendure J, Nickerson DA, Bamshad MJ. PMID: 23273567.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    44. A newly recognized syndrome with characteristic facial features, skeletal dysplasia, and developmental delay. Am J Med Genet A. 2012 Aug; 158A(8):1815-22. Baratela WA, Bober MB, Tiller GE, Okenfuss E, Ditro C, Duker A, Krakow D, Stabley DL, Sol-Church K, Mackenzie W, Lachman R, Scott CI. PMID: 22711505.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    45. Exome sequencing identifies PDE4D mutations in acrodysostosis. Am J Hum Genet. 2012 Apr 06; 90(4):746-51. Lee H, Graham JM, Rimoin DL, Lachman RS, Krejci P, Tompson SW, Nelson SF, Krakow D, Cohn DH. PMID: 22464252.
      View in: PubMed   Mentions: 38     Fields:    Translation:HumansCells
    46. Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling. Am J Hum Genet. 2012 Mar 09; 90(3):550-7. Merrill AE, Sarukhanov A, Krejci P, Idoni B, Camacho N, Estrada KD, Lyons KM, Deixler H, Robinson H, Chitayat D, Curry CJ, Lachman RS, Wilcox WR, Krakow D. PMID: 22387015.
      View in: PubMed   Mentions: 22     Fields:    Translation:HumansCells
    47. Disease-associated mutations in the actin-binding domain of filamin B cause cytoplasmic focal accumulations correlating with disease severity. Hum Mutat. 2012 Apr; 33(4):665-73. Daniel PB, Morgan T, Alanay Y, Bijlsma E, Cho TJ, Cole T, Collins F, David A, Devriendt K, Faivre L, Ikegawa S, Jacquemont S, Jesic M, Krakow D, Liebrecht D, Maitz S, Marlin S, Morin G, Nishikubo T, Nishimura G, Prescott T, Scarano G, Shafeghati Y, Skovby F, Tsutsumi S, Whiteford M, Zenker M, Robertson SP. PMID: 22190451.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    48. Dominant and recessive forms of fibrochondrogenesis resulting from mutations at a second locus, COL11A2. Am J Med Genet A. 2012 Feb; 158A(2):309-14. Tompson SW, Faqeih EA, Ala-Kokko L, Hecht JT, Miki R, Funari T, Funari VA, Nevarez L, Krakow D, Cohn DH. PMID: 22246659.
      View in: PubMed   Mentions: 5     Fields:    Translation:HumansCells
    49. The importance of conventional radiography in the mutational analysis of skeletal dysplasias (the TRPV4 mutational family). Pediatr Radiol. 2012 Jan; 42(1):15-23. Nemec SF, Cohn DH, Krakow D, Funari VA, Rimoin DL, Lachman RS. PMID: 21863289.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    50. Mutations in the TGFß binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias. Am J Hum Genet. 2011 Jul 15; 89(1):7-14. Le Goff C, Mahaut C, Wang LW, Allali S, Abhyankar A, Jensen S, Zylberberg L, Collod-Beroud G, Bonnet D, Alanay Y, Brady AF, Cordier MP, Devriendt K, Genevieve D, Kiper PÖ, Kitoh H, Krakow D, Lynch SA, Le Merrer M, Mégarbane A, Mortier G, Odent S, Polak M, Rohrbach M, Sillence D, Stolte-Dijkstra I, Superti-Furga A, Rimoin DL, Topouchian V, Unger S, Zabel B, Bole-Feysot C, Nitschke P, Handford P, Casanova JL, Boileau C, Apte SS, Munnich A, Cormier-Daire V. PMID: 21683322.
      View in: PubMed   Mentions: 50     Fields:    Translation:HumansCells
    51. Nosology and classification of genetic skeletal disorders: 2010 revision. Am J Med Genet A. 2011 May; 155A(5):943-68. Warman ML, Cormier-Daire V, Hall C, Krakow D, Lachman R, LeMerrer M, Mortier G, Mundlos S, Nishimura G, Rimoin DL, Robertson S, Savarirayan R, Sillence D, Spranger J, Unger S, Zabel B, Superti-Furga A. PMID: 21438135.
      View in: PubMed   Mentions: 166     Fields:    Translation:Humans
    52. The skeleton and musculature on foetal MRI. Insights Imaging. 2011 Jun; 2(3):309-318. Nemec U, Nemec SF, Krakow D, Brugger PC, Malinger G, Graham JM, Rimoin DL, Prayer D. PMID: 22347955.
      View in: PubMed   Mentions:
    53. Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene. Am J Hum Genet. 2010 Nov 12; 87(5):708-12. Tompson SW, Bacino CA, Safina NP, Bober MB, Proud VK, Funari T, Wangler MF, Nevarez L, Ala-Kokko L, Wilcox WR, Eyre DR, Krakow D, Cohn DH. PMID: 21035103.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    54. BMPER mutation in diaphanospondylodysostosis identified by ancestral autozygosity mapping and targeted high-throughput sequencing. Am J Hum Genet. 2010 Oct 08; 87(4):532-7. Funari VA, Krakow D, Nevarez L, Chen Z, Funari TL, Vatanavicharn N, Wilcox WR, Rimoin DL, Nelson SF, Cohn DH. PMID: 20869035.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansAnimalsCells
    55. The skeletal dysplasias. Genet Med. 2010 Jun; 12(6):327-41. Krakow D, Rimoin DL. PMID: 20556869.
      View in: PubMed   Mentions: 32     Fields:    Translation:Humans
    56. Generalized connective tissue disease in Crtap-/- mouse. PLoS One. 2010 May 11; 5(5):e10560. Baldridge D, Lennington J, Weis M, Homan EP, Jiang MM, Munivez E, Keene DR, Hogue WR, Pyott S, Byers PH, Krakow D, Cohn DH, Eyre DR, Lee B, Morello R. PMID: 20485499.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansAnimalsCells
    57. Dominant TRPV4 mutations in nonlethal and lethal metatropic dysplasia. Am J Med Genet A. 2010 May; 152A(5):1169-77. Camacho N, Krakow D, Johnykutty S, Katzman PJ, Pepkowitz S, Vriens J, Nilius B, Boyce BF, Cohn DH. PMID: 20425821.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansCells
    58. Mutations in the gene encoding the RER protein FKBP65 cause autosomal-recessive osteogenesis imperfecta. Am J Hum Genet. 2010 Apr 09; 86(4):551-9. Alanay Y, Avaygan H, Camacho N, Utine GE, Boduroglu K, Aktas D, Alikasifoglu M, Tuncbilek E, Orhan D, Bakar FT, Zabel B, Superti-Furga A, Bruckner-Tuderman L, Curry CJ, Pyott S, Byers PH, Eyre DR, Baldridge D, Lee B, Merrill AE, Davis EC, Cohn DH, Akarsu N, Krakow D. PMID: 20362275.
      View in: PubMed   Mentions: 93     Fields:    Translation:Humans
    59. Postnatal growth retardation, facial dysmorphism, spondylocarpal synostosis, cardiac defect, and inner ear malformation (cardiospondylocarpofacial syndrome?)--a distinct syndrome? Am J Med Genet A. 2010 Mar; 152A(3):539-46. Sousa SB, Baujat G, Abadie V, Bonnet D, Sidi D, Munnich A, Krakow D, Cormier-Daire V. PMID: 20186786.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    60. Lethal skeletal dysplasia in mice and humans lacking the golgin GMAP-210. N Engl J Med. 2010 Jan 21; 362(3):206-16. Smits P, Bolton AD, Funari V, Hong M, Boyden ED, Lu L, Manning DK, Dwyer ND, Moran JL, Prysak M, Merriman B, Nelson SF, Bonafé L, Superti-Furga A, Ikegawa S, Krakow D, Cohn DH, Kirchhausen T, Warman ML, Beier DR. PMID: 20089971.
      View in: PubMed   Mentions: 43     Fields:    Translation:HumansAnimalsCells
    61. The Erlenmeyer flask bone deformity in the skeletal dysplasias. Am J Med Genet A. 2009 Jun; 149A(6):1334-45. Faden MA, Krakow D, Ezgu F, Rimoin DL, Lachman RS. PMID: 19444897.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    62. Ciliary abnormalities due to defects in the retrograde transport protein DYNC2H1 in short-rib polydactyly syndrome. Am J Hum Genet. 2009 Apr; 84(4):542-9. Merrill AE, Merriman B, Farrington-Rock C, Camacho N, Sebald ET, Funari VA, Schibler MJ, Firestein MH, Cohn ZA, Priore MA, Thompson AK, Rimoin DL, Nelson SF, Cohn DH, Krakow D. PMID: 19361615.
      View in: PubMed   Mentions: 50     Fields:    Translation:HumansCells
    63. Mutations in the gene encoding the calcium-permeable ion channel TRPV4 produce spondylometaphyseal dysplasia, Kozlowski type and metatropic dysplasia. Am J Hum Genet. 2009 Mar; 84(3):307-15. Krakow D, Vriens J, Camacho N, Luong P, Deixler H, Funari TL, Bacino CA, Irons MB, Holm IA, Sadler L, Okenfuss EB, Janssens A, Voets T, Rimoin DL, Lachman RS, Nilius B, Cohn DH. PMID: 19232556.
      View in: PubMed   Mentions: 58     Fields:    Translation:Humans
    64. Guidelines for the prenatal diagnosis of fetal skeletal dysplasias. Genet Med. 2009 Feb; 11(2):127-33. Krakow D, Lachman RS, Rimoin DL. PMID: 19265753.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansAnimals
    65. A recessive skeletal dysplasia, SEMD aggrecan type, results from a missense mutation affecting the C-type lectin domain of aggrecan. Am J Hum Genet. 2009 Jan; 84(1):72-9. Tompson SW, Merriman B, Funari VA, Fresquet M, Lachman RS, Rimoin DL, Nelson SF, Briggs MD, Cohn DH, Krakow D. PMID: 19110214.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCells
    66. CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta. Hum Mutat. 2008 Dec; 29(12):1435-42. Baldridge D, Schwarze U, Morello R, Lennington J, Bertin TK, Pace JM, Pepin MG, Weis M, Eyre DR, Walsh J, Lambert D, Green A, Robinson H, Michelson M, Houge G, Lindman C, Martin J, Ward J, Lemyre E, Mitchell JJ, Krakow D, Rimoin DL, Cohn DH, Byers PH, Lee B. PMID: 18566967.
      View in: PubMed   Mentions: 81     Fields:    Translation:Humans
    67. Evaluation of prenatal-onset osteochondrodysplasias by ultrasonography: a retrospective and prospective analysis. Am J Med Genet A. 2008 Aug 01; 146A(15):1917-24. Krakow D, Alanay Y, Rimoin LP, Lin V, Wilcox WR, Lachman RS, Rimoin DL. PMID: 18627037.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    68. Spondylocarpotarsal synostosis: long-term follow-up of a case due to FLNB mutations. Am J Med Genet A. 2008 May 01; 146A(9):1230-3. Brunetti-Pierri N, Esposito V, De Brasi D, Mattiacci DM, Krakow D, Lee B, Salerno M. PMID: 18386804.
      View in: PubMed   Mentions: 2     Fields:    Translation:HumansCells
    69. Expanded clinical spectrum of spondylocarpotarsal synostosis syndrome and possible manifestation in a heterozygous father. Am J Med Genet A. 2008 Mar 15; 146A(6):779-83. Mitter D, Krakow D, Farrington-Rock C, Meinecke P. PMID: 18257094.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    70. The skeletal dysplasias: clinical-molecular correlations. Ann N Y Acad Sci. 2007 Nov; 1117:302-9. Rimoin DL, Cohn D, Krakow D, Wilcox W, Lachman RS, Alanay Y. PMID: 18056050.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    71. Disruption of the Flnb gene in mice phenocopies the human disease spondylocarpotarsal synostosis syndrome. Hum Mol Genet. 2008 Mar 01; 17(5):631-41. Farrington-Rock C, Kirilova V, Dillard-Telm L, Borowsky AD, Chalk S, Rock MJ, Cohn DH, Krakow D. PMID: 17635842.
      View in: PubMed   Mentions: 19     Fields:    Translation:HumansAnimalsCells
    72. Cartilage-selective genes identified in genome-scale analysis of non-cartilage and cartilage gene expression. BMC Genomics. 2007 Jun 12; 8:165. Funari VA, Day A, Krakow D, Cohn ZA, Chen Z, Nelson SF, Cohn DH. PMID: 17565682.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    73. Angulated femurs and the skeletal dysplasias: experience of the International Skeletal Dysplasia Registry (1988-2006). Am J Med Genet A. 2007 Jun 01; 143A(11):1159-68. Alanay Y, Krakow D, Rimoin DL, Lachman RS. PMID: 17486589.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    74. Polyvalvular disease in a fetus with normal chromosomes. Congenit Heart Dis. 2007 May-Jun; 2(3):214-7. Miller M, Krakow D, Pepkowitz S. PMID: 18377469.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    75. Fibroblast growth factors 1, 2, 17, and 19 are the predominant FGF ligands expressed in human fetal growth plate cartilage. Pediatr Res. 2007 Mar; 61(3):267-72. Krejci P, Krakow D, Mekikian PB, Wilcox WR. PMID: 17314681.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansAnimalsCells
    76. Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycans. Hum Mutat. 2007 Mar; 28(3):209-21. Marini JC, Forlino A, Cabral WA, Barnes AM, San Antonio JD, Milgrom S, Hyland JC, Körkkö J, Prockop DJ, De Paepe A, Coucke P, Symoens S, Glorieux FH, Roughley PJ, Lund AM, Kuurila-Svahn K, Hartikka H, Cohn DH, Krakow D, Mottes M, Schwarze U, Chen D, Yang K, Kuslich C, Troendle J, Dalgleish R, Byers PH. PMID: 17078022.
      View in: PubMed   Mentions: 177     Fields:    Translation:HumansCells
    77. Frontometaphyseal dysplasia: mutations in FLNA and phenotypic diversity. Am J Med Genet A. 2006 Aug 15; 140(16):1726-36. Robertson SP, Jenkins ZA, Morgan T, Adès L, Aftimos S, Boute O, Fiskerstrand T, Garcia-Miñaur S, Grix A, Green A, Der Kaloustian V, Lewkonia R, McInnes B, van Haelst MM, Mancini G, Macini G, Illés T, Mortier G, Newbury-Ecob R, Nicholson L, Scott CI, Ochman K, Brozek I, Shears DJ, Superti-Furga A, Suri M, Whiteford M, Wilkie AO, Krakow D. PMID: 16835913.
      View in: PubMed   Mentions: 25     Fields:    Translation:HumansCells
    78. Mutations in two regions of FLNB result in atelosteogenesis I and III. Hum Mutat. 2006 Jul; 27(7):705-10. Farrington-Rock C, Firestein MH, Bicknell LS, Superti-Furga A, Bacino CA, Cormier-Daire V, Le Merrer M, Baumann C, Roume J, Rump P, Verheij JB, Sweeney E, Rimoin DL, Lachman RS, Robertson SP, Cohn DH, Krakow D. PMID: 16752402.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansCells
    79. A molecular and clinical study of Larsen syndrome caused by mutations in FLNB. J Med Genet. 2007 Feb; 44(2):89-98. Bicknell LS, Farrington-Rock C, Shafeghati Y, Rump P, Alanay Y, Alembik Y, Al-Madani N, Firth H, Karimi-Nejad MH, Kim CA, Leask K, Maisenbacher M, Moran E, Pappas JG, Prontera P, de Ravel T, Fryns JP, Sweeney E, Fryer A, Unger S, Wilson LC, Lachman RS, Rimoin DL, Cohn DH, Krakow D, Robertson SP. PMID: 16801345.
      View in: PubMed   Mentions: 29     Fields:    Translation:HumansCells
    80. Genetic evaluation of suspected osteogenesis imperfecta (OI). Genet Med. 2006 Jun; 8(6):383-8. Byers PH, Krakow D, Nunes ME, Pepin M. PMID: 16778601.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    81. Terminal phalangeal accessory ossification center of the thumb: an additional radiographic finding in Larsen syndrome. Pediatr Radiol. 2006 Sep; 36(9):970-3. Alanay Y, Utine GE, Lachman RS, Krakow D, Tuncbilek E. PMID: 16715218.
      View in: PubMed   Mentions: 2     Fields:    Translation:Humans
    82. Dysregulation of chondrogenesis in human cleidocranial dysplasia. Am J Hum Genet. 2005 Aug; 77(2):305-12. Zheng Q, Sebald E, Zhou G, Chen Y, Wilcox W, Lee B, Krakow D. PMID: 15952089.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansAnimalsCells
    83. MED, COMP, multilayered and NEIN: an overview of multiple epiphyseal dysplasia. Pediatr Radiol. 2005 Feb; 35(2):116-23. Lachman RS, Krakow D, Cohn DH, Rimoin DL. PMID: 15503005.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    84. A transcriptional profile of human fetal cartilage. Matrix Biol. 2004 Aug; 23(5):299-307. Pogue R, Sebald E, King L, Kronstadt E, Krakow D, Cohn DH. PMID: 15464362.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    85. Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis. Nat Genet. 2004 Apr; 36(4):405-10. Krakow D, Robertson SP, King LM, Morgan T, Sebald ET, Bertolotto C, Wachsmann-Hogiu S, Acuna D, Shapiro SS, Takafuta T, Aftimos S, Kim CA, Firth H, Steiner CE, Cormier-Daire V, Superti-Furga A, Bonafe L, Graham JM, Grix A, Bacino CA, Allanson J, Bialer MG, Lachman RS, Rimoin DL, Cohn DH. PMID: 14991055.
      View in: PubMed   Mentions: 72     Fields:    Translation:Cells
    86. Isolation of a new member of the ADP-ribosylation like factor gene family, ARL8, from a cartilage cDNA library. Gene. 2003 Jun 05; 311:147-51. Sebald E, Krueger R, King LM, Cohn DH, Krakow D. PMID: 12853149.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansAnimalsCells
    87. Analysis of clones from a human cartilage cDNA library provides insight into chondrocyte gene expression and identifies novel candidate genes for the osteochondrodysplasias. Mol Genet Metab. 2003 May; 79(1):34-42. Krakow D, Sebald ET, Pogue R, Rimoin LP, King L, Cohn DH. PMID: 12765844.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    88. Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia. Eur J Hum Genet. 2003 Mar; 11(3):265-70. Melkoniemi M, Koillinen H, Männikkö M, Warman ML, Pihlajamaa T, Kääriäinen H, Rautio J, Hukki J, Stofko JA, Cisneros GJ, Krakow D, Cohn DH, Kere J, Ala-Kokko L. PMID: 12673280.
      View in: PubMed   Mentions: 13     Fields:    Translation:Humans
    89. Mental retardation and abnormal skeletal development (Dyggve-Melchior-Clausen dysplasia) due to mutations in a novel, evolutionarily conserved gene. Am J Hum Genet. 2003 Feb; 72(2):419-28. Cohn DH, Ehtesham N, Krakow D, Unger S, Shanske A, Reinker K, Powell BR, Rimoin DL. PMID: 12491225.
      View in: PubMed   Mentions: 7     Fields:    Translation:HumansCells
    Deborah's Networks
    Concepts (381)
    Derived automatically from this person's publications.
    Explore
    _
    Co-Authors (14)
    People in Profiles who have published with this person.
    Explore
    _
    Similar People (60)
    People who share similar concepts with this person.
    Explore
    _
    Same Department
    Search Department
    _
    ↑