Mary L. Marazita
Title
Cited by
Cited by
Year
Cleft lip and palate: understanding genetic and environmental influences
MJ Dixon, ML Marazita, TH Beaty, JC Murray
Nature Reviews Genetics 12 (3), 167-178, 2011
12372011
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
6582004
Genetic epidemiological studies of early‐onset deafness in the US school‐age population
ML Marazita, LM Ploughman, B Rawlings, E Remington, KS Arnos, ...
American journal of medical genetics 46 (5), 486-491, 1993
6071993
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, 2010
4762010
Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip
F Rahimov, ML Marazita, A Visel, ME Cooper, MJ Hitchler, M Rubini, ...
Nature genetics 40 (11), 1341, 2008
4282008
Detectable clonal mosaicism from birth to old age and its relationship to cancer
CC Laurie, CA Laurie, K Rice, KF Doheny, LR Zelnick, CP McHugh, ...
Nature genetics 44 (6), 642, 2012
4092012
Idiopathic congenital central hypoventilation syndrome: analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in …
DE Weese‐Mayer, EM Berry‐Kravis, L Zhou, BS Maher, JM Silvestri, ...
American journal of medical genetics Part A 123 (3), 267-278, 2003
3452003
Anthropometric precision and accuracy of digital three-dimensional photogrammetry: comparing the Genex and 3dMD imaging systems with one another and with direct anthropometry
SM Weinberg, S Naidoo, DP Govier, RA Martin, AA Kane, ML Marazita
Journal of Craniofacial Surgery 17 (3), 477-483, 2006
3142006
Maternal serum 25-hydroxyvitamin D concentrations are associated with small-for-gestational age births in white women
LM Bodnar, JM Catov, JM Zmuda, ME Cooper, MS Parrott, JM Roberts, ...
The Journal of nutrition 140 (5), 999-1006, 2010
2982010
Impaired FGF signaling contributes to cleft lip and palate
BM Riley, MA Mansilla, J Ma, S Daack-Hirsch, BS Maher, ...
Proceedings of the National Academy of Sciences 104 (11), 4512-4517, 2007
2942007
The PhenX Toolkit: get the most from your measures
CM Hamilton, LC Strader, JG Pratt, D Maiese, T Hendershot, RK Kwok, ...
American journal of epidemiology 174 (3), 253-260, 2011
2742011
Medical sequencing of candidate genes for nonsyndromic cleft lip and palate
AR Vieira, JR Avila, S Daack-Hirsch, E Dragan, TM Félix, F Rahimov, ...
PLoS genetics 1 (6), 2005
2682005
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
2642004
Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis
BS Maher, ML Marazita, RE Ferrell, MM Vanyukov
Psychiatric Genetics 12 (4), 207-215, 2002
2642002
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci
KU Ludwig, E Mangold, S Herms, S Nowak, H Reutter, A Paul, J Becker, ...
Nature genetics 44 (9), 968, 2012
2602012
Evidence for autosomal dominant inheritance and race‐specific heterogeneity in early‐onset periodontitis
ML Marazita, JA Burmeister, JC Gunsolley, TE Koertge, K Lake, ...
Journal of periodontology 65 (6), 623-630, 1994
2501994
Genetics of cleft lip and cleft palate
EJ Leslie, ML Marazita
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2013
2412013
A specific requirement for PDGF-C in palate formation and PDGFR-α signaling
H Ding, X Wu, H Boström, I Kim, N Wong, B Tsoi, M O'Rourke, GY Koh, ...
Nature genetics 36 (10), 1111-1116, 2004
2402004
A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1
TC Hart, Y Zhang, MC Gorry, PS Hart, M Cooper, ML Marazita, JM Marks, ...
The American Journal of Human Genetics 70 (4), 943-954, 2002
2302002
Waardenberg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: First report of the WS consortium
LA Farrer, KM Grundfast, J Amos, KS Arnos, JH Asher, P Beighton, ...
American journal of human genetics 50 (5), 902, 1992
2281992
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