Marcella Devoto

发表

Advances in family-based association analysis. Introduction.

Derek Gordon, Marcella Devoto, 2008, Human heredity.

Polymorphisms of α-adducin and salt sensitivity in patients with essential hypertension

Cristina Barlassina, Paolo Manunta, Daniele Cusi, 1997, The Lancet.

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome.

Stephan Eliez, Tingwei Guo, Xiaowu Gai, 2015, American journal of human genetics.

Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2

Aldo Quattrone, Antonio Gambardella, Anthony P. Monaco, 2000, Nature Genetics.

Identification of ALK as a major familial neuroblastoma predisposition gene

John M. Maris, Nicholas J. Schork, Ali Torkamani, 2008, Nature.

A Novel Susceptibility Locus for Type 1 Diabetes on Chr12q13 Identified by a Genome-Wide Association Study

Constantin Polychronakos, Luc Marchand, Margaret L. Lawson, 2008, Diabetes.

Integration of Omics Data in Genetic Epidemiology

E. Génin, M. Devoto, Emmanuelle Génin, 2015, Human Heredity.

Integrative genomics identifies LMO1 as a neuroblastoma oncogene

Nazneen Rahman, Sharon J. Diskin, John M. Maris, 2011, Nature.

Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Susanne Walitza, Aribert Rothenberger, Takeshi Sakurai, 2011, Nature Genetics.

Common variations in BARD1 influence susceptibility to high-risk neuroblastoma

Nazneen Rahman, Sharon J. Diskin, John M. Maris, 2009, Nature Genetics.

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

I. Krantz, M. Bamshad, C. Morris, 2004, Nature Genetics.

Copy number variation at 1q21.1 associated with neuroblastoma

Sharon J. Diskin, John M. Maris, Struan F. A. Grant, 2009, Nature.

Genetic mapping of quantitative trait loci for disease-related phenotypes.

Mario Falchi, M. Devoto, M. Falchi, 2012, Methods in molecular biology.

Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.

Nazneen Rahman, Joseph T. Glessner, Hakon Hakonarson, 2008, The New England journal of medicine.

25 MUTATIONS IN STXBP3 CONTRIBUTE TO VERY EARLY ONSET OF IBD, IMMUNODEFICIENCY AND HEARING LOSS

Christopher A. Cassa, Dana Vuzman, Ágnes Tóth-Petróczy, 2018 .

Next-Generation Linkage Analysis

Veronica J. Vieland, V. Vieland, M. Devoto, 2011, Human Heredity.

Variants of DENND1B associated with asthma in children.

Ingo Ruczinski, James Flory, Terri H Beaty, 2010, The New England journal of medicine.

Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellum

Joseph T. Glessner, Hakon Hakonarson, Francesca Lantieri, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22

Aldo Quattrone, Antonio Gambardella, Anthony P. Monaco, 2000 .