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Neuregulin 3 ( ) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition

Molecular psychiatry, 2011-08, Vol.16 (8), p.860-866

2011

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A newly discovered founder population: the Roma/Gypsies

BioEssays, 2005-10, Vol.27 (10), p.1084-1094

2005

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KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment

Journal of cellular and molecular medicine, 2008-09, Vol.12 (5a), p.1672-1676

2008

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Polymorphisms associated with normal memory variation also affect memory impairment in schizophrenia

Genes, brain and behavior, 2011-06, Vol.10 (4), p.410-417

2011

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Origins and Divergence of the Roma (Gypsies)

American journal of human genetics, 2001-12, Vol.69 (6), p.1314-1331

2001

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Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia

Molecular psychiatry, 2012-12, Vol.17 (12), p.1328-1339

2012

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Evaluation of association of SNPs in the TNF alpha gene region with schizophrenia

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-04, Vol.144B (3), p.318-324

2007

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Vlax Roma history: what do coalescent-based methods tell us?

European journal of human genetics : EJHG, 2004-04, Vol.12 (4), p.285-292

2004

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Genetic substructure in South African Bantu-speakers: Evidence from autosomal DNA and Y-chromosome studies

American journal of physical anthropology, 2002-10, Vol.119 (2), p.175-185

2002

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The Effective Mutation Rate at Y Chromosome Short Tandem Repeats, with Application to Human Population-Divergence Time

American journal of human genetics, 2004-01, Vol.74 (1), p.50-61

2004

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BIN1 founder mutation in the Spanish gypsy population is the most frequent cause of adult onset centronuclear myopathies in the south of Spain

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S172-S173

2017

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P.258 - BIN1 founder mutation in the Spanish gypsy population is the most frequent cause of adult onset centronuclear myopathies in the south of Spain

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S172-S173

2017

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Mutation History of the Roma/Gypsies

American journal of human genetics, 2004-10, Vol.75 (4), p.596-609

2004

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LONGEVITY KLOTHO GENE POLYMORPHISM AND THE RISK OF DEMENTIA IN OLDER MEN

Innovation in aging, 2017-07, Vol.1 (suppl_1), p.906-906

2017

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A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus

Human genetics, 1998-08, Vol.103 (2), p.211-227

1998

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Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease

Human mutation, 2003-08, Vol.22 (2), p.129-135

2003

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Genealogy and genes: tracing the founding fathers of Tristan da Cunha

European journal of human genetics : EJHG, 2003-09, Vol.11 (9), p.705-709

2003

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Y-chromosomal evidence for a strong reduction in male population size of Yakuts

Human genetics, 2002-02, Vol.110 (2), p.198-200

2002

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The molecular characterization of Gaucher disease in South Africa

Early human development, 1997-10, Vol.49 (3), p.241-241

1997

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Beware the scorpion parabuthus

Central African journal of medicine, 1990-04, Vol.36 (4), p.114

1990

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The molecular characterization of Gaucher disease in South Africa

Clinical genetics, 1996-08, Vol.50 (2), p.78-84

1996

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Bilateral fracture of the femoral neck as a direct result of electrocution shock

Central African journal of medicine, 1994-12, Vol.40 (12), p.355

1994

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Interleukin-5–producing group 2 innate lymphoid cells control eosinophilia induced by interleukin-2 therapy

Blood, 2014-12, Vol.124 (24), p.3572-3576

2014

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HIV-associated psoriasis: pathogenesis, clinical features, and management

The Lancet infectious diseases, 2010-07, Vol.10 (7), p.470-478

2010

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Neuregulin 3 ( ) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition

A newly discovered founder population: the Roma/Gypsies

KIBRA genetic polymorphism influences episodic memory in later life, but does not increase the risk of mild cognitive impairment

Polymorphisms associated with normal memory variation also affect memory impairment in schizophrenia

Origins and Divergence of the Roma (Gypsies)

Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia

Evaluation of association of SNPs in the TNF alpha gene region with schizophrenia

Vlax Roma history: what do coalescent-based methods tell us?

Genetic substructure in South African Bantu-speakers: Evidence from autosomal DNA and Y-chromosome studies

The Effective Mutation Rate at Y Chromosome Short Tandem Repeats, with Application to Human Population-Divergence Time

BIN1 founder mutation in the Spanish gypsy population is the most frequent cause of adult onset centronuclear myopathies in the south of Spain

P.258 - BIN1 founder mutation in the Spanish gypsy population is the most frequent cause of adult onset centronuclear myopathies in the south of Spain

Mutation History of the Roma/Gypsies

Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome

LONGEVITY KLOTHO GENE POLYMORPHISM AND THE RISK OF DEMENTIA IN OLDER MEN

A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus

Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease

Genealogy and genes: tracing the founding fathers of Tristan da Cunha

Y-chromosomal evidence for a strong reduction in male population size of Yakuts

The molecular characterization of Gaucher disease in South Africa

Beware the scorpion parabuthus

The molecular characterization of Gaucher disease in South Africa

Bilateral fracture of the femoral neck as a direct result of electrocution shock

Interleukin-5–producing group 2 innate lymphoid cells control eosinophilia induced by interleukin-2 therapy

HIV-associated psoriasis: pathogenesis, clinical features, and management

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