Andrew Lidral
Andrew Lidral
שותפות לא ידועה
כתובת אימייל מאומתת בדומיין
צוטט על ידי
צוטט על ידי
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
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
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
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
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
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
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
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
Progress toward discerning the genetics of cleft lip
AC Lidral, LM Moreno
Current opinion in pediatrics 17 (6), 731, 2005
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24. 2, 17q23 and 19q13
EJ Leslie, JC Carlson, JR Shaffer, E Feingold, G Wehby, CA Laurie, ...
Human molecular genetics 25 (13), 2862-2872, 2016
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
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
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
המערכת אינה יכולה לבצע את הפעולה כעת. נסה שוב מאוחר יותר.
מאמרים 1–20