Andrew Lidral
Andrew Lidral
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Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
S Kondo, BC Schutte, RJ Richardson, BC Bjork, AS Knight, Y Watanabe, ...
Nature genetics 32 (2), 285-289, 2002
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate
TM Zucchero, ME Cooper, BS Maher, S Daack-Hirsch, B Nepomuceno, ...
New England Journal of Medicine 351 (8), 769-780, 2004
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
TH Beaty, JC Murray, ML Marazita, RG Munger, I Ruczinski, JB Hetmanski, ...
Nature genetics 42 (6), 525-529, 2010
Association of MSX1 and TGFB3 with nonsyndromic clefting in humans
AC Lidral, PA Romitti, AM Basart, T Doetschman, NJ Leysens, ...
The American Journal of Human Genetics 63 (2), 557-568, 1998
Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: evaluation of genotype‐environment interactions from a population …
PA Romitti, AC Lidral, RG Munger, S Daack‐Hirsch, TL Burns, JC Murray
Teratology 59 (1), 39-50, 1999
Development of the upper lip: morphogenetic and molecular mechanisms
R Jiang, JO Bush, AC Lidral
Developmental dynamics: an official publication of the American Association …, 2006
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35
ML Marazita, JC Murray, AC Lidral, M Arcos-Burgos, ME Cooper, ...
The American Journal of Human Genetics 75 (2), 161-173, 2004
The role of MSX1 in human tooth agenesis
AC Lidral, BC Reising
Journal of dental research 81 (4), 274-278, 2002
Studies of the candidate genes TGFB2, MSX1, TGFA, and TGFB3 in the etiology of cleft lip and palate in the Philippines
AC Lidral, JC Murray, KH Buetow, AM Basart, H Schearer, R Shiang, ...
The Cleft palate-craniofacial journal 34 (1), 1-6, 1997
Autosomal dominant craniometaphyseal dysplasia is caused by mutations in the transmembrane protein ANK
E Reichenberger, V Tiziani, S Watanabe, L Park, Y Ueki, C Santanna, ...
The American Journal of Human Genetics 68 (6), 1321-1326, 2001
Mutations in BMP4 are associated with subepithelial, microform, and overt cleft lip
S Suzuki, ML Marazita, ME Cooper, N Miwa, A Hing, A Jugessur, ...
The American Journal of Human Genetics 84 (3), 406-411, 2009
Genetic association studies of cleft lip and/or palate with hypodontia outside the cleft region
RL Slayton, L Williams, JC Murray, JJ Wheeler, AC Lidral, CJ Nishimura
The Cleft palate-craniofacial journal 40 (3), 274-279, 2003
TBX22 mutations are a frequent cause of cleft palate
ACB Marcano, K Doudney, C Braybrook, R Squires, MA Patton, MM Lees, ...
Journal of medical genetics 41 (1), 68-74, 2004
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association …
ML Marazita, AC Lidral, JC Murray, LL Field, BS Maher, TG McHenry, ...
Human heredity 68 (3), 151-170, 2009
Progress toward discerning the genetics of cleft lip
AC Lidral, LM Moreno
Current opinion in pediatrics 17 (6), 731, 2005
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate
LM Moreno, MA Mansilla, SA Bullard, ME Cooper, TD Busch, J Machida, ...
Human molecular genetics 18 (24), 4879-4896, 2009
Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test
DM Juriloff, MJ Harris, AP McMahon, TJ Carroll, AC Lidral
Birth Defects Research Part A: Clinical and Molecular Teratology 76 (8), 574-579, 2006
Expression of Wnt9b and activation of canonical Wnt signaling during midfacial morphogenesis in mice
Y Lan, RC Ryan, Z Zhang, SA Bullard, JO Bush, KM Maltby, AC Lidral, ...
Developmental dynamics: an official publication of the American Association …, 2006
Association of transforming growth-factor alpha gene polymorphisms with nonsyndromic cleft palate only (CPO).
R Shiang, AC Lidral, HH Ardinger, KH Buetow, PA Romitti, RG Munger, ...
American journal of human genetics 53 (4), 836, 1993
Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q
H El-Shanti, AC Lidral, N Jarrah, L Druhan, K Ajlouni
The American Journal of Human Genetics 66 (4), 1229-1236, 2000
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