Lista de obras -

A Comparison Between Two Screening Approaches for ASD Among Toddlers in Israel.

artículo científico publicado en 2018

A brain region-specific predictive gene map for autism derived by profiling a reference gene set

artículo científico publicado en 2011

A pooled analysis of three studies evaluating genetic variation in innate immunity genes and non-Hodgkin lymphoma risk

artículo científico publicado en 2011

A pooled investigation of Toll-like receptor gene variants and risk of non-Hodgkin lymphoma

artículo científico publicado en 2008

A probabilistic classifier for olfactory receptor pseudogenes

artículo científico publicado en 2006

A systematic variant annotation approach for ranking genes associated with autism spectrum disorders

artículo científico publicado en 2016

Age-related crossover in breast cancer incidence rates between black and white ethnic groups

artículo científico publicado en 2008

An analysis of growth, differentiation and apoptosis genes with risk of renal cancer

artículo científico publicado en 2009

Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk

artículo científico publicado en 2009

Apolipoprotein E/C1 locus variants modify renal cell carcinoma risk

artículo científico publicado en 2009

Association between genetic variants in the 8q24 cancer risk regions and circulating levels of androgens and sex hormone-binding globulin

artículo científico publicado en 2010

Brief Report: The Negev Hospital-University-Based (HUB) Autism Database

artículo científico publicado en 2017

Cell-type-specific neuroanatomy of cliques of autism-related genes in the mouse brain

artículo científico publicado en 2015

Characteristics Associated with Drug Prescription and Compliance Among Young Children with Autism Spectrum Disorder

artículo científico publicado en 2017

Co-expression profiling of autism genes in the mouse brain

artículo científico publicado en 2013

Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk

artículo científico publicado en 2009

Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut

artículo científico publicado en 2010

Comprehensive analysis of 5-aminolevulinic acid dehydrogenase (ALAD) variants and renal cell carcinoma risk among individuals exposed to lead

artículo científico publicado en 2011

Different noses for different people

artículo científico publicado en 2003

Genetic determinants of serum lipid levels in Chinese subjects: a population-based study in Shanghai, China

artículo científico publicado en 2009

Genetic elucidation of human hyperosmia to isovaleric acid

artículo científico publicado en 2007

Genetic variation in Th1/Th2 pathway genes and risk of non-Hodgkin lymphoma: a pooled analysis of three population-based case-control studies

artículo científico publicado en 2011

Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies

artículo científico publicado en 2009

Genetic variation in cell cycle and apoptosis related genes and multiple myeloma risk

artículo científico publicado en 2009

Large-scale pathway-based analysis of bladder cancer genome-wide association data from five studies of European background

artículo científico publicado en 2012

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

PGA: power calculator for case-control genetic association analyses.

artículo científico publicado en 2008

PTEN identified as important risk factor of chronic obstructive pulmonary disease

artículo científico publicado en 2009

Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade

artículo científico publicado en 2010

Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway

artículo científico publicado en 2008

Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma in a pooled analysis of three studies

artículo científico publicado en 2010

Polymorphisms in complement system genes and risk of non-Hodgkin lymphoma

artículo científico publicado en 2011

Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China

artículo científico publicado en 2009

Polymorphisms in pattern-recognition genes in the innate immunity system and risk of non-Hodgkin lymphoma.

artículo científico publicado en 2012

Population differences in haplotype structure within a human olfactory receptor gene cluster

artículo científico publicado en 2002

Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database

artículo científico publicado en 2013

Re: Racial disparities in cancer survival among randomized clinical trials of the Southwest Oncology Group

artículo científico publicado en 2010

Risk of non-Hodgkin lymphoma associated with germline variation in genes that regulate the cell cycle, apoptosis, and lymphocyte development

artículo científico publicado en 2009

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

artículo científico publicado en 2013

Sleep disturbances are associated with specific sensory sensitivities in children with autism

artículo científico publicado en 2018

The Unique Evolutionary Signature of Genes Associated with Autism Spectrum Disorder

artículo científico publicado en 2016

The association between inflammation-related genes and serum androgen levels in men: the prostate, lung, colorectal, and ovarian study

artículo científico publicado en 2011

Underlying causes of the black-white racial disparity in breast cancer mortality: a population-based analysis

artículo científico publicado en 2009

Variants in blood pressure genes and the risk of renal cell carcinoma

artículo científico publicado en 2010

Variation in innate immunity genes and risk of multiple myeloma

artículo científico publicado en 2011

Variations in chromosomes 9 and 6p21.3 with risk of non-Hodgkin lymphoma

artículo científico publicado en 2010

Lista de obras de

A Comparison Between Two Screening Approaches for ASD Among Toddlers in Israel.

A brain region-specific predictive gene map for autism derived by profiling a reference gene set

A pooled analysis of three studies evaluating genetic variation in innate immunity genes and non-Hodgkin lymphoma risk

A pooled investigation of Toll-like receptor gene variants and risk of non-Hodgkin lymphoma

A probabilistic classifier for olfactory receptor pseudogenes

A systematic variant annotation approach for ranking genes associated with autism spectrum disorders

Age-related crossover in breast cancer incidence rates between black and white ethnic groups

An analysis of growth, differentiation and apoptosis genes with risk of renal cancer

Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk

Apolipoprotein E/C1 locus variants modify renal cell carcinoma risk

Association between genetic variants in the 8q24 cancer risk regions and circulating levels of androgens and sex hormone-binding globulin

Brief Report: The Negev Hospital-University-Based (HUB) Autism Database

Cell-type-specific neuroanatomy of cliques of autism-related genes in the mouse brain

Characteristics Associated with Drug Prescription and Compliance Among Young Children with Autism Spectrum Disorder

Co-expression profiling of autism genes in the mouse brain

Common gene variants in the tumor necrosis factor (TNF) and TNF receptor superfamilies and NF-kB transcription factors and non-Hodgkin lymphoma risk

Common single nucleotide polymorphisms in immunoregulatory genes and multiple myeloma risk among women in Connecticut

Comprehensive analysis of 5-aminolevulinic acid dehydrogenase (ALAD) variants and renal cell carcinoma risk among individuals exposed to lead

Different noses for different people

Genetic determinants of serum lipid levels in Chinese subjects: a population-based study in Shanghai, China

Genetic elucidation of human hyperosmia to isovaleric acid

Genetic variation in Th1/Th2 pathway genes and risk of non-Hodgkin lymphoma: a pooled analysis of three population-based case-control studies

Genetic variation in caspase genes and risk of non-Hodgkin lymphoma: a pooled analysis of 3 population-based case-control studies

Genetic variation in cell cycle and apoptosis related genes and multiple myeloma risk

Large-scale pathway-based analysis of bladder cancer genome-wide association data from five studies of European background

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

PGA: power calculator for case-control genetic association analyses.

PTEN identified as important risk factor of chronic obstructive pulmonary disease

Pathway analysis of breast cancer genome-wide association study highlights three pathways and one canonical signaling cascade

Pathway-based evaluation of 380 candidate genes and lung cancer susceptibility suggests the importance of the cell cycle pathway

Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma in a pooled analysis of three studies

Polymorphisms in complement system genes and risk of non-Hodgkin lymphoma

Polymorphisms in innate immunity genes and lung cancer risk in Xuanwei, China

Polymorphisms in pattern-recognition genes in the innate immunity system and risk of non-Hodgkin lymphoma.

Population differences in haplotype structure within a human olfactory receptor gene cluster

Prioritization of Copy Number Variation Loci Associated with Autism from AutDB-An Integrative Multi-Study Genetic Database

Re: Racial disparities in cancer survival among randomized clinical trials of the Southwest Oncology Group

Risk of non-Hodgkin lymphoma associated with germline variation in genes that regulate the cell cycle, apoptosis, and lymphocyte development

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

Sleep disturbances are associated with specific sensory sensitivities in children with autism

The Unique Evolutionary Signature of Genes Associated with Autism Spectrum Disorder

The association between inflammation-related genes and serum androgen levels in men: the prostate, lung, colorectal, and ovarian study

Underlying causes of the black-white racial disparity in breast cancer mortality: a population-based analysis

Variants in blood pressure genes and the risk of renal cell carcinoma

Variation in innate immunity genes and risk of multiple myeloma

Variations in chromosomes 9 and 6p21.3 with risk of non-Hodgkin lymphoma