Publications by authors named "Peter Chines"

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Systematic phenotype and genotype characterization of Moebius syndrome.
Bryn D Webb, Julie A Jurgens, Narisu Narisu, Zhongyang Zhang, Brenda J Barry, Peter S Chines

Genet Med Open· May 2025

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Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Alan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, Wai-Man Chan, Elke de Boer, Peter S Chines

Nat Genet· July 2023

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Hydroa vacciniforme-like lymphoproliferative disorder: an EBV disease with a low risk of systemic illness in whites.
Jeffrey I Cohen, Irini Manoli, Kennichi Dowdell, Tammy A Krogmann, Deborah Tamura, Peter S Chines

Blood· June 2019

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Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle.
D Leland Taylor, Anne U Jackson, Narisu Narisu, Gibran Hemani, Michael R Erdos, Peter S Chines

Proc Natl Acad Sci U S A· May 2019

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Multiomic Profiling Identifies cis-Regulatory Networks Underlying Human Pancreatic β Cell Identity and Function.
Nathan Lawlor, Eladio J Márquez, Peter Orchard, Narisu Narisu, Muhammad Saad Shamim, Peter S Chines

Cell Rep· January 2019

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Interactions between genetic variation and cellular environment in skeletal muscle gene expression.
D Leland Taylor, David A Knowles, Laura J Scott, Andrea H Ramirez, Francesco Paolo Casale, Peter S Chines

PLoS One· July 2018

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Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
Tanya M Teslovich, Daniel Seung Kim, Xianyong Yin, Alena Stancáková, Anne U Jackson, Peter S Chines

Hum Mol Genet· May 2018

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BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues.
Luli S Zou, Michael R Erdos, D Leland Taylor, Peter S Chines, Arushi Varshney

BMC Genomics· May 2018

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Somatic mosaicism of an intragenic FANCB duplication in both fibroblast and peripheral blood cells observed in a Fanconi anemia patient leads to milder phenotype.
Rajalakshmi S Asur, Danielle C Kimble, Francis P Lach, Moonjung Jung, Frank X Donovan, Peter Chines

Mol Genet Genomic Med· January 2018

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Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Goo Jun, Alisa Manning, Marcio Almeida, Matthew Zawistowski, Andrew R Wood, Peter S Chines

Proc Natl Acad Sci U S A· January 2018

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Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Jason Flannick, Christian Fuchsberger, Anubha Mahajan, Tanya M Teslovich, Vineeta Agarwala, Peter S Chines

Sci Data· January 2018

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Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.
Jason Flannick, Christian Fuchsberger, Anubha Mahajan, Tanya M Teslovich, Vineeta Agarwala, Peter S Chines

Sci Data· December 2017

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An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans.
Robert A Scott, Laura J Scott, Reedik Mägi, Letizia Marullo, Kyle J Gaulton, Peter S Chines

Diabetes· November 2017

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Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
James P Davis, Jeroen R Huyghe, Adam E Locke, Anne U Jackson, Xueling Sim, Peter S Chines

PLoS Genet· October 2017

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Correction: Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Mariaelisa Graff, Robert A Scott, Anne E Justice, Kristin L Young, Mary F Feitosa, Peter S Chines

PLoS Genet· August 2017

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A Low-Frequency Inactivating Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.
Alisa Manning, Heather M Highland, Jessica Gasser, Xueling Sim, Taru Tukiainen, Peter S Chines

Diabetes· July 2017

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A defect in myoblast fusion underlies Carey-Fineman-Ziter syndrome.
Silvio Alessandro Di Gioia, Samantha Connors, Norisada Matsunami, Jessica Cannavino, Matthew F Rose, Peter S Chines

Nat Commun· July 2017

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Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits.
Anne E Justice, Thomas W Winkler, Mary F Feitosa, Misa Graff, Virginia A Fisher, Peter S Chines

Nat Commun· April 2017

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Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults.
Mariaelisa Graff, Robert A Scott, Anne E Justice, Kristin L Young, Mary F Feitosa, Peter S Chines

PLoS Genet· April 2017

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A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome.
Daniel Z Bar, Martin F Arlt, Joan F Brazier, Wendy E Norris, Susan E Campbell, Peter Chines

J Med Genet· March 2017

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Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.
Mete Civelek, Ying Wu, Calvin Pan, Chelsea K Raulerson, Arthur Ko, Peter S Chines

Am J Hum Genet· March 2017

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Genetic regulatory signatures underlying islet gene expression and type 2 diabetes.
Arushi Varshney, Laura J Scott, Ryan P Welch, Michael R Erdos, Peter S Chines

Proc Natl Acad Sci U S A· February 2017

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A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape.
Janina S Ried, Janina Jeff M, Audrey Y Chu, Jennifer L Bragg-Gresham, Jenny van Dongen, Peter S Chines

Nat Commun· November 2016

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The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals.
Georg B Ehret, Teresa Ferreira, Daniel I Chasman, Anne U Jackson, Ellen M Schmidt, Peter S Chines

Nat Genet· October 2016

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The genetic architecture of type 2 diabetes.
Christian Fuchsberger, Jason Flannick, Tanya M Teslovich, Anubha Mahajan, Vineeta Agarwala, Peter S Chines

Nature· August 2016

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