Lista de obras - Axel M Hillmer - Dominio Público Uruguay

A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer

artículo científico publicado en 2012

A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

artículo científico publicado en 2008

A genome-wide association study in 574 schizophrenia trios using DNA pooling

scientific journal article

Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology

article

Detection of chromosomal breakpoints in patients with developmental delay and speech disorders

artículo científico publicado en 2014

Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing

artículo científico publicado en 2018

Epigenomic profiling of primary gastric adenocarcinoma reveals super-enhancer heterogeneity

artículo científico publicado en 2016

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: variable phenotypic expression in three affected sisters from Mexican ancestry

artículo científico publicado en 2014

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

artículo científico publicado en 2008

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

artículo científico publicado en 2017

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia

artículo científico publicado en 2005

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

artículo científico publicado en 2011

Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26

artículo científico publicado en 2008

Genomic landscape of lung adenocarcinoma in East Asians

artículo científico publicado en 2020

High-depth sequencing of over 750 genes supports linear progression of primary tumors and metastases in most patients with liver-limited metastatic colorectal cancer

artículo científico publicado en 2015

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

artículo científico publicado en 2003

Linking Cancer Stem Cell Plasticity to Therapeutic Resistance-Mechanism and Novel Therapeutic Strategies in Esophageal Cancer

scientific article published on 17 June 2020

Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

article

Methionine is a metabolic dependency of tumor-initiating cells

scientific article published on 06 May 2019

Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia

Patient-specific driver gene prediction and risk assessment through integrated network analysis of cancer omics profiles.

artículo científico publicado en 2015

Publisher Correction: Methionine is a metabolic dependency of tumor-initiating cells

artículo científico publicado en 2019

Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness

artículo científico publicado en 2009

Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors

artículo científico publicado en 2017

Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases

artículo científico publicado en 2012

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

artículo científico publicado en 2005

Susceptibility variants for male-pattern baldness on chromosome 20p11.

artículo científico publicado en 2008

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

artículo científico publicado en 2009

The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata

artículo científico publicado en 2007

The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function

artículo científico publicado en 2007

Whole-genome sequencing of asian lung cancers: second-hand smoke unlikely to be responsible for higher incidence of lung cancer among Asian never-smokers

artículo científico publicado en 2014

Lista de obras de Axel M Hillmer

A common BIM deletion polymorphism mediates intrinsic resistance and inferior responses to tyrosine kinase inhibitors in cancer

A genome-wide association study for late-onset Alzheimer's disease using DNA pooling

A genome-wide association study in 574 schizophrenia trios using DNA pooling

Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology

Detection of chromosomal breakpoints in patients with developmental delay and speech disorders

Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencing

Epigenomic profiling of primary gastric adenocarcinoma reveals super-enhancer heterogeneity

Familial hypomagnesemia with hypercalciuria and nephrocalcinosis: variable phenotypic expression in three affected sisters from Mexican ancestry

G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26

Genomic landscape of lung adenocarcinoma in East Asians

High-depth sequencing of over 750 genes supports linear progression of primary tumors and metastases in most patients with liver-limited metastatic colorectal cancer

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

Linking Cancer Stem Cell Plasticity to Therapeutic Resistance-Mechanism and Novel Therapeutic Strategies in Esophageal Cancer

Loss-of-Function Mutations in the Filaggrin Gene and Alopecia Areata: Strong Risk Factor for a Severe Course of Disease in Patients Comorbid for Atopic Disease

Methionine is a metabolic dependency of tumor-initiating cells

Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia

Patient-specific driver gene prediction and risk assessment through integrated network analysis of cancer omics profiles.

Publisher Correction: Methionine is a metabolic dependency of tumor-initiating cells

Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness

Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors

Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia

Susceptibility variants for male-pattern baldness on chromosome 20p11.

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

The R620W polymorphism in PTPN22 confers general susceptibility for the development of alopecia areata

The two most common alleles of the coding GGN repeat in the androgen receptor gene cause differences in protein function

Whole-genome sequencing of asian lung cancers: second-hand smoke unlikely to be responsible for higher incidence of lung cancer among Asian never-smokers