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MHC transmission: insights into gender bias in MS susceptibility

Neurology, 2011-01, Vol.76 (3), p.242

2011

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Risk alleles for multiple sclerosis in multiplex families

Neurology, 2009-06, Vol.72 (23), p.1984

2009

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Parent-of-origin effect in multiple sclerosis: observations from interracial matings

Neurology, 2009-08, Vol.73 (8), p.602

2009

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Parent-of-origin effect in multiple sclerosis: observations in half-siblings

The Lancet (British edition), 2004-05, Vol.363 (9423), p.1773-1774

2004

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Age of puberty and the risk of multiple sclerosis: a population based study

European journal of neurology, 2009-03, Vol.16 (3), p.342-347

2009

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A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesia

European journal of medical genetics, 2021-05, Vol.64 (5), p.104193-104193, Article 104193

2021

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Sex ratio of multiple sclerosis and clinical phenotype

European journal of neurology, 2010-04, Vol.17 (4), p.634-637

2010

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A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia

Neurology, 2005-07, Vol.65 (1), p.156

2005

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Evidence for genetic basis of multiple sclerosis

The Lancet (British edition), 1996-06, Vol.347 (9017), p.1728-1730

1996

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HLA-DRB1 and month of birth in multiple sclerosis

Neurology, 2009-12, Vol.73 (24), p.2107

2009

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Microsatellites and genome scans — A GAMES postscript

Journal of neuroimmunology, 2007-10, Vol.190 (1), p.5-7

2007

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The role of hereditary spastic paraplegia related genes in multiple sclerosis : A study of disease susceptibility and clinical outcome

Journal of neurology, 2007-09, Vol.254 (9), p.1221-1226

2007

Volltextzugriff (PDF)

Two females with mutations in USP9X highlight the variable expressivity of the intellectual disability syndrome

European journal of medical genetics, 2017-07, Vol.60 (7), p.359-364

2017

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Biallelic mutations at PPARG cause a congenital, generalized lipodystrophy similar to the Berardinelli–Seip syndrome

European journal of medical genetics, 2014-09, Vol.57 (9), p.524-526

2014

Volltextzugriff (PDF)

Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13

Neurology, 2002-10, Vol.59 (7), p.1099

2002

Volltextzugriff (PDF)

Genetics of Multiple Sclerosis

Human molecular genetics, 1997-01, Vol.6 (10), p.1693-1698

1997

Volltextzugriff (PDF)

A multigenerational family with multiple sclerosis

Brain (London, England : 1878), 2002-07, Vol.125 (7), p.1474-1482

2002

Volltextzugriff (PDF)

Analysis of 45 candidate genes for disease modifying activity in multiple sclerosis

Journal of neurology, 2008-08, Vol.255 (8), p.1215-1219

2008

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An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group

Human molecular genetics, 2004-05, Vol.13 (10), p.1005-1015

2004

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Evidence of Linkage with HLA-DR in DRB115-Negative Families with Multiple Sclerosis

American journal of human genetics, 2001-10, Vol.69 (4), p.900-903

2001

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A novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsy

Neurogenetics, 2018, Vol.19 (1), p.61-65

2018

Volltextzugriff (PDF)

No effect of APOE and PVRL2 on the clinical outcome of multiple sclerosis

Journal of neuroimmunology, 2007-05, Vol.186 (1), p.156-160

2007

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No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study

Journal of neuroimmunology, 2002-02, Vol.123 (1), p.193-198

2002

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Follow-up investigation of 12 proposed linkage regions in multiple sclerosis

Genes and immunity, 2006-07, Vol.7 (5), p.366-371

2006

Volltextzugriff (PDF)

Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1

Journal of human genetics, 2017-06, Vol.62 (6), p.661-663

2017

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MHC transmission: insights into gender bias in MS susceptibility

Risk alleles for multiple sclerosis in multiplex families

Parent-of-origin effect in multiple sclerosis: observations from interracial matings

Parent-of-origin effect in multiple sclerosis: observations in half-siblings

Age of puberty and the risk of multiple sclerosis: a population based study

A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesia

Sex ratio of multiple sclerosis and clinical phenotype

A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia

Evidence for genetic basis of multiple sclerosis

HLA-DRB1 and month of birth in multiple sclerosis

Microsatellites and genome scans — A GAMES postscript

The role of hereditary spastic paraplegia related genes in multiple sclerosis : A study of disease susceptibility and clinical outcome

Two females with mutations in USP9X highlight the variable expressivity of the intellectual disability syndrome

Biallelic mutations at PPARG cause a congenital, generalized lipodystrophy similar to the Berardinelli–Seip syndrome

Migraine with aura is not linked to the FHM gene CACNA1A or the chromosomal region, 19p13

Genetics of Multiple Sclerosis

A multigenerational family with multiple sclerosis

Analysis of 45 candidate genes for disease modifying activity in multiple sclerosis

An extended genome scan in 442 Canadian multiple sclerosis-affected sibships: a report from the Canadian Collaborative Study Group

Evidence of Linkage with HLA-DR in DRB115-Negative Families with Multiple Sclerosis

A novel mutation in LAMC3 associated with generalized polymicrogyria of the cortex and epilepsy

No effect of APOE and PVRL2 on the clinical outcome of multiple sclerosis

No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study

Follow-up investigation of 12 proposed linkage regions in multiple sclerosis

Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1

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