Lista de obras - Lan Xiong - Dominio Público Uruguay

A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1

scientific article published in Scientific Reports

Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome

artículo científico publicado en 2015

Association study of essential tremor genetic loci in Parkinson's disease

artículo científico publicado en 2018

Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1.

artículo científico publicado en 2009

Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

artículo científico publicado en 2010

De novo variants in sporadic cases of childhood onset schizophrenia

artículo científico publicado en 2015

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

artículo científico publicado en 2010

Family study of restless legs syndrome in Quebec, Canada: clinical characterization of 671 familial cases

artículo científico publicado en 2010

Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians

artículo científico publicado en 2007

Genetic markers of Restless Legs Syndrome in Parkinson disease

artículo científico publicado en 2015

Genetics of restless legs syndrome

artículo científico publicado en 2016

Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population

artículo científico publicado en 2018

Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1

scientific journal article

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

artículo científico publicado en 2007

Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population

artículo científico publicado en 2015

Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families

artículo científico publicado en 2007

Mutational analysis of neurotensin in familial restless legs syndrome

artículo científico publicado en 2004

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

artículo científico publicado en 2008

Progress in Genetic Studies of Tourette's Syndrome

artículo científico publicado en 2017

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population

artículo científico publicado en 2016

Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis

artículo científico publicado en 2011

Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity

artículo científico publicado en 2005

TOX3 Variants Are Involved in Restless Legs Syndrome and Parkinson's Disease with Opposite Effects

artículo científico publicado en 2018

The 14q restless legs syndrome locus in the French Canadian population

artículo científico publicado en 2004

Where are the missing pieces of the schizophrenia genetics puzzle?

artículo científico publicado en 2011

Lista de obras de Lan Xiong

A direct interaction between two Restless Legs Syndrome predisposing genes: MEIS1 and SKOR1

Analysis of functional GLO1 variants in the BTBD9 locus and restless legs syndrome

Association study of essential tremor genetic loci in Parkinson's disease

Autosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1.

Correction: Genome-Wide Association Study Identifies Novel Restless Legs Syndrome Susceptibility Loci on 2p14 and 16q12.1

De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

De novo variants in sporadic cases of childhood onset schizophrenia

Direct measure of the de novo mutation rate in autism and schizophrenia cohorts

Family study of restless legs syndrome in Quebec, Canada: clinical characterization of 671 familial cases

Genetic association studies of neurotensin gene and restless legs syndrome in French Canadians

Genetic markers of Restless Legs Syndrome in Parkinson disease

Genetics of restless legs syndrome

Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population

Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1

Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions

Increased missense mutation burden of Fatty Acid metabolism related genes in nunavik inuit population

Molecular genetic studies of DMT1 on 12q in French-Canadian restless legs syndrome patients and families

Mutational analysis of neurotensin in familial restless legs syndrome

PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome

Progress in Genetic Studies of Tourette's Syndrome

RNF213 Is Associated with Intracranial Aneurysms in the French-Canadian Population

Restless legs syndrome-associated MEIS1 risk variant influences iron homeostasis

Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity

TOX3 Variants Are Involved in Restless Legs Syndrome and Parkinson's Disease with Opposite Effects

The 14q restless legs syndrome locus in the French Canadian population

Where are the missing pieces of the schizophrenia genetics puzzle?