Identity by descent analysis identifies founder events and links SOD1 familial and sporadic ALS cases

Evidence for polygenic and oligogenic basis of Australian sporadic amyotrophic lateral sclerosis

(2020) Emily P McCann et al.   JOURNAL OF MEDICAL GENETICS

Lifetime Risk and Heritability of Amyotrophic Lateral Sclerosis

(2019) Marie Ryan et al.   JAMA Neurology

Amyotrophic Lateral Sclerosis: An Update for 2018

(2018) Björn Oskarsson et al.   MAYO CLINIC PROCEEDINGS

Identity-by-descent analyses for measuring population dynamics and selection in recombining pathogens

(2018) Lyndal Henden et al.   PLoS Genetics

Predictive genetic testing for amyotrophic lateral sclerosis and frontotemporal dementia: genetic counselling considerations

(2017) Ashley Crook et al.   Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Identity by descent fine mapping of familial adult myoclonus epilepsy (FAME) to 2p11.2–2q11.2

(2016) Lyndal Henden et al.   HUMAN GENETICS

Gene discovery in amyotrophic lateral sclerosis: implications for clinical management

(2016) Ammar Al-Chalabi et al.   Nature Reviews Neurology

Identical by descent L1CAM mutation in two apparently unrelated families with intellectual disability without L1 syndrome

(2015) Marie Shaw et al.   European Journal of Medical Genetics

Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis

(2015) Satoshi Yamashita et al.   Translational Neurodegeneration

Dating Rare Mutations from Small Samples with Dense Marker Data

(2014) Luke C. Gandolfo et al.   GENETICS

Accurate and Robust Prediction of Genetic Relationship from Whole-Genome Sequences

(2014) Hong Li et al.   PLoS One

State of play in amyotrophic lateral sclerosis genetics

(2013) Alan E Renton et al.   NATURE NEUROSCIENCE

Founder effect hypothesis of D11Y SOD1 mutation in Italian amyotrophic lateral sclerosis patients

(2012) Serena Lattante et al.   Amyotrophic Lateral Sclerosis

Detection of identity by descent using next-generation whole genome sequencing data

(2012) Shu-Yi Su et al.   BMC BIOINFORMATICS

Amyotrophic lateral sclerosis

(2011) Matthew C Kiernan et al.   LANCET

High-Resolution Detection of Identity by Descent in Unrelated Individuals

(2010) Sharon R. Browning et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Inference of Unexpected Genetic Relatedness among Individuals in HapMap Phase III

(2010) Trevor J. Pemberton et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

(2010) A. McKenna et al.   GENOME RESEARCH

An estimate of amyotrophic lateral sclerosis heritability using twin data

(2010) A. Al-Chalabi et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Fast and accurate short read alignment with Burrows-Wheeler transform

(2009) H. Li et al.   BIOINFORMATICS

Genetics of motor neuron disorders: new insights into pathogenic mechanisms

(2009) Patrick A. Dion et al.   NATURE REVIEWS GENETICS

Age and founder effect of SOD1 A4V mutation causing ALS

(2009) M. Saeed et al.   NEUROLOGY

SOD1 gene mutations in ALS patients from British Columbia, Canada: Clinical features, neurophysiology and ethical issues in management

(2008) Andrew Eisen et al.   Amyotrophic Lateral Sclerosis

Relatedness mapping and tracts of relatedness for genome-wide data in the presence of linkage disequilibrium

(2008) Anders Albrechtsen et al.   GENETIC EPIDEMIOLOGY

Whole population, genome-wide mapping of hidden relatedness

(2008) A. Gusev et al.   GENOME RESEARCH