Andrew Lidral
Andrew Lidral
שותפות לא ידועה
כתובת אימייל מאומתת בדומיין uiowa.edu
כותרת
צוטט על ידי
צוטט על ידי
שנה
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
9372002
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
7162004
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
5662010
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
4491998
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
3352006
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
3211999
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
2832004
The role of MSX1 in human tooth agenesis
AC Lidral, BC Reising
Journal of dental research 81 (4), 274-278, 2002
2812002
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
2401997
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
2062009
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
1952001
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
1802003
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
1592004
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
1572009
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
1552009
Progress toward discerning the genetics of cleft lip
AC Lidral, LM Moreno
Current opinion in pediatrics 17 (6), 731, 2005
1512005
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
1442016
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
1402006
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
1352006
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
1342000
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מאמרים 1–20