FAT4 identified as a potential modifier of orofacial cleft laterality
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T. Beaty | S. Weinberg | M. Marazita | E. Feingold | R. Lipinski | Miranda R. Sun | E. Leslie | J. Carlson | Jenna C. Carlson | J. Murray | M. Epstein | Sarah W Curtis | Daniel Chang | J. C. Murray
[1] T. Beaty,et al. The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lip , 2021, HGG advances.
[2] Haixin Wang,et al. Genetic factors define CPO and CLO subtypes of nonsyndromicorofacial cleft , 2019, PLoS genetics.
[3] Dr. M. Kuftinec. Dental Anomalies , 2019, International Journal of Paediatric Dentistry.
[4] C. Francks,et al. The molecular genetics of hand preference revisited , 2018, Scientific Reports.
[5] T. Beaty,et al. A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals , 2019, Genetic epidemiology.
[6] J. Noonan,et al. High-Resolution Epigenomic Atlas of Human Embryonic Craniofacial Development , 2018, Cell reports.
[7] R. Hennekam,et al. Van Maldergem syndrome and Hennekam syndrome: Further delineation of allelic phenotypes , 2018, American journal of medical genetics. Part A.
[8] T. Beaty,et al. Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes , 2017, Genetic epidemiology.
[9] T. Beaty,et al. Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families , 2017, Molecular Genetics & Genomic Medicine.
[10] M. Marazita,et al. Sonic hedgehog regulation of Foxf2 promotes cranial neural crest mesenchyme proliferation and is disrupted in cleft lip morphogenesis , 2017, Development.
[11] T. Beaty,et al. Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity , 2017, Nature Communications.
[12] R. Lipinski,et al. Gli2 gene-environment interactions contribute to the etiological complexity of holoprosencephaly: evidence from a mouse model , 2016, Development.
[13] R. T. Lie,et al. A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3. , 2016, American journal of human genetics.
[14] R. T. Lie,et al. 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. , 2016, Human molecular genetics.
[15] M. Rubini,et al. Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene , 2016, PLoS genetics.
[16] R. Lipinski,et al. A Simple and Reliable Method for Early Pregnancy Detection in Inbred Mice. , 2015, Journal of the American Association for Laboratory Animal Science : JAALAS.
[17] Joris M. Mooij,et al. MAGMA: Generalized Gene-Set Analysis of GWAS Data , 2015, PLoS Comput. Biol..
[18] 田原 康玄,et al. 生活習慣病とgenome-wide association study , 2015 .
[19] Carson C Chow,et al. Second-generation PLINK: rising to the challenge of larger and richer datasets , 2014, GigaScience.
[20] R. Hennekam,et al. Hennekam syndrome can be caused by FAT4 mutations and be allelic to Van Maldergem syndrome , 2014, Human Genetics.
[21] Sahar Mansour,et al. Mutations in genes encoding the cadherin receptor-ligand pair DCHS1 and FAT4 disrupt cerebral cortical development , 2013, Nature Genetics.
[22] Mark R. Morris,et al. Perlman Syndrome: Overgrowth, Wilms Tumor Predisposition and DIS3L2. , 2013, American Journal of Medical Genetics. Part C, Seminars in Medical Genetics.
[23] W. Chung,et al. Association of candidate genes with nonsyndromic clefts in Honduran and Colombian populations , 2012, The Laryngoscope.
[24] S. Cichon,et al. Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci , 2012, Nature Genetics.
[25] A. Jugessur,et al. Genetics of Nonsyndromic Orofacial Clefts , 2012, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
[26] P. Visscher,et al. GCTA: a tool for genome-wide complex trait analysis. , 2011, American journal of human genetics.
[27] Peter Kraft,et al. Quality control and quality assurance in genotypic data for genome‐wide association studies , 2010, Genetic epidemiology.
[28] Michael Boehnke,et al. LocusZoom: regional visualization of genome-wide association scan results , 2010, Bioinform..
[29] Holger Schwender,et al. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 , 2010, Nature Genetics.
[30] Ş. Evirgen,et al. Dental anomalies in individuals with cleft lip and/or palate. , 2010, European journal of orthodontics.
[31] M. Nöthen,et al. Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients , 2009, American journal of medical genetics. Part A.
[32] Bernhard Horsthemke,et al. Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 , 2009, Nature Genetics.
[33] Manfred Gessler,et al. Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease , 2008, Nature Genetics.
[34] R. T. Lie,et al. Familial risk of oral clefts by morphological type and severity: population based cohort study of first degree relatives , 2008, BDJ.
[35] K. Gundlach,et al. Epidemiological studies on the frequency of clefts in Europe and world-wide. , 2006, Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery.
[36] G. Bobashev,et al. Description of the methodology used in an ongoing pediatric care interventional study of children born with cleft lip and palate in South America [NCT00097149] , 2006, BMC pediatrics.
[37] Jeffrey C Murray,et al. Long term follow up study of survival associated with cleft lip and palate at birth , 2004, BMJ : British Medical Journal.
[38] B. Costa,et al. Dental anomalies of the permanent lateral incisors and prevalence of hypodontia outside the cleft area in complete unilateral cleft lip and palate. , 2003, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
[39] Jeremy W. Dale,et al. Analysis of Sequence Data , 2003 .
[40] P. Mortensen,et al. Facial clefting and psychiatric diseases: a follow-up of the Danish 1936-1987 Facial Cleft cohort. , 2002, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
[41] P. Mortensen,et al. Facial Clefting and Psychiatric Diseases: A Follow-Up of the Danish 1936–1987 Facial Cleft Cohort , 2002 .
[42] L. T. das Neves,et al. Dental development of permanent lateral incisor in complete unilateral cleft lip and palate. , 2002, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
[43] L. Jocelyn,et al. Cognition, communication, and hearing in young children with cleft lip and palate and in control children: a longitudinal study. , 1996, Pediatrics.
[44] A. E. Poole. Genetics of cleft lip and cleft palate. , 1975, Dental clinics of North America.
[45] T. Beaty,et al. Identifying Genetic Sources of Phenotypic Heterogeneity in Orofacial Clefts by Targeted Sequencing. , 2017, Birth defects research.
[46] Jeffrey C Murray,et al. Risk of breast cancer in families with cleft lip and palate. , 2012, Annals of epidemiology.
[47] Hong Wang,et al. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA 4 , 2010 .
[48] S. Cichon,et al. Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate , 2010, Nature Genetics.
[49] G. Wehby,et al. The impact of orofacial clefts on quality of life and healthcare use and costs. , 2010, Oral diseases.
[50] M. Marazita,et al. AXIS inhibition protein 2, orofacial clefts and a family history of cancer. , 2009, Journal of the American Dental Association.
[51] G. Licht,et al. Description of Methodology , 2004 .
[52] B. Tüysüz,et al. [Hennekam syndrome]. , 1998, Archives de pediatrie : organe officiel de la Societe francaise de pediatrie.
[53] J. Burn,et al. Congenital anomalies in twins. , 1986, Seminars in perinatology.
[54] H B Wong,et al. Genetics of cleft lip and cleft palate. , 1987, The Journal of the Singapore Paediatric Society.
[55] R. Khesin,et al. Molecular Genetics , 1968, Springer Berlin Heidelberg.