Mary L Marazita

发表

Inferring Disease Risk Genes from Sequencing Data in Multiplex Pedigrees Through Sharing of Rare Variants

Ingo Ruczinski, Alexandre Bureau, Ferdouse Begum, 2018, bioRxiv.

Rapid Testing of SNPs and Gene–Environment Interactions in Case–Parent Trio Data Based on Exact Analytic Parameter Estimation

Holger Schwender, Ingo Ruczinski, Margaret A Taub, 2012, Biometrics.

Using the PhenX Toolkit to Add Standard Measures to a Study

Huaqin Pan, Mary L Marazita, Carol M Hamilton, 2011, Current protocols in human genetics.

Anthropometric Precision and Accuracy of Digital Three-Dimensional Photogrammetry: Comparing the Genex and 3dMD Imaging Systems with One Another and with Direct Anthropometry

Sybill Naidoo, Mary L Marazita, S. Weinberg, 2006, The Journal of craniofacial surgery.

Heritability of Face Shape in Twins: A Preliminary Study using 3D Stereophotogrammetry and Geometric Morphometrics.

Mary L Marazita, Brion S Maher, T. Parsons, 2013, Dentistry 3000.

Genome-wide mapping of global-to-local genetic effects on human facial shape

Paul Suetens, Julie D. White, Dirk Vandermeulen, 2018, Nature Genetics.

Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.

Ingo Ruczinski, Qunyuan Zhang, Ferdouse Begum, 2015, American journal of human genetics.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA 4

Hong Wang, Holger Schwender, Ingo Ruczinski, 2010 .

Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.

Andres Metspalu, Paul Scheet, Alexander Teumer, 2013, Human molecular genetics.

Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology

Chung How Kau, Washington Mio, Jeffrey C Murray, 2016, PLoS genetics.

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Holger Schwender, Ingo Ruczinski, Jacqueline B Hetmanski, 2010, Nature Genetics.

Demographic and prenatal factors of patients with cleft lip and cleft palate. A pilot study.

Shelly Abramowicz, Mary L Marazita, M. Marazita, 2003, Journal of the American Dental Association.

Evidence for gene‐environment interaction in a genome wide study of nonsyndromic cleft palate

Holger Schwender, Ingo Ruczinski, Jacqueline B Hetmanski, 2011, Genetic epidemiology.

Digital Three-Dimensional Photogrammetry: Evaluation of Anthropometric Precision and Accuracy Using a Genex 3D Camera System

Mary L Marazita, Nicole M. Scott, S. Weinberg, 2004, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Whole exome association of rare deletions in multiplex oral cleft families

Ingo Ruczinski, Alexandre Bureau, Hasan Albacha-Hejazi, 2017, Genetic epidemiology.

Dopamine system genes and attention deficit hyperactivity disorder: a meta-analysis

Mary L Marazita, Brion S Maher, B. Maher, 2002, Psychiatric genetics.

Erratum: A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4

Holger Schwender, Alan F Scott, Jeffrey C Murray, 2010, Nature Genetics.

The FaceBase Consortium: a comprehensive program to facilitate craniofacial research.

Harry Hochheiser, Axel Visel, Jeffrey C Murray, 2011, Developmental biology.

Using genetics to test the causal relationship of total adiposity and periodontitis: Mendelian randomization analyses in the Gene-Lifestyle Interactions and Dental Endpoints (GLIDE) Consortium.

Peter Kraft, Alexander Teumer, Tom M Palmer, 2015, International journal of epidemiology.

Characterization of large structural genetic mosaicism in human autosomes.

William Wheeler, Nan Hu, Peter Kraft, 2015, American journal of human genetics.

Identifying genetic risk loci for diabetic complications and showing evidence for heterogeneity of type 1 diabetes based on complications risk

Mary L Marazita, Manika Govil, Nandita Mukhopadhyay, 2018, PloS one.

Phenotype harmonization and cross‐study collaboration in GWAS consortia: the GENEVA experience

Peter Kraft, Mary L Marazita, Kathleen Barnes, 2011, Genetic epidemiology.

A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk

Holger Schwender, Ingo Ruczinski, Alan F Scott, 2014, BMC Genetics.

Sudden Infant Death Syndrome: Case-Control Frequency Differences at Genes Pertinent to Early Autonomic Nervous System Embryologic Development

Lili Zhou, Debra E Weese-Mayer, Elizabeth M Berry-Kravis, 2004, Pediatric Research.

An ordered subset approach to including covariates in the transmission disequilibrium test

Hervé Perdry, Mary L Marazita, Marie-Claude Babron, 2007, BMC proceedings.

Three‐dimensional morphometric analysis of craniofacial shape in the unaffected relatives of individuals with nonsyndromic orofacial clefts: A possible marker for genetic susceptibility

Mary L Marazita, Brion S Maher, Joan T Richtsmeier, 2008, American journal of medical genetics. Part A.

Gene‐environment interplay in common complex diseases: forging an integrative model—recommendations from an NIH workshop

Peter Kraft, Kimberly McAllister, Eric Boerwinkle, 2011, Genetic epidemiology.

Sudden Infant Death Syndrome: Review of implicated genetic factors

Michael J Ackerman, Debra E Weese-Mayer, Elizabeth M Berry-Kravis, 2007, American journal of medical genetics. Part A.

A mutation in the SOS1 gene causes hereditary gingival fibromatosis type 1.

Mary L Marazita, M. Marazita, M. Gorry, 2002, American journal of human genetics.