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Comparative analysis in cynomolgus macaque identifies a novel human MHC locus controlling platelet blood counts independently of BAK1

Journal of thrombosis and haemostasis, 2013-02, Vol.11 (2), p.384-386

2013

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Recurrent Mutations in a Single Exon Encoding the Evolutionarily Conserved Olfactomedin-Homology Domain of TIGR in Familial Open-Angle Glaucoma

Human molecular genetics, 1997-11, Vol.6 (12), p.2091-2097

1997

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Linkage of HLA to myasthenia gravis and genetic heterogeneity depending on anti-titin antibodies

Neurology, 2001-11, Vol.57 (9), p.1555-1560

2001

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A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family

Human reproduction (Oxford), 2018-06, Vol.33 (6), p.1034-1037

2018

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Genetic influences on the end-stage effector phase of arthritis

The Journal of experimental medicine, 2001-08, Vol.194 (3), p.321-330

2001

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CYP1B1 mutations in French patients with early-onset primary open-angle glaucoma

Journal of medical genetics, 2004-09, Vol.41 (9), p.647-651

2004

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Insulin-Dependent Diabetes Mellitus (IDDM) Is Associated with CTLA4 Polymorphisms in Multiple Ethnic Groups

Human molecular genetics, 1997-08, Vol.6 (8), p.1275-1282

1997

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Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes

Human reproduction (Oxford), 2022-05, Vol.37 (6), p.1334-1350

2022

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Apoptosis as a mechanism of keratinocyte death in toxic epidermal necrolysis

British journal of dermatology (1951), 1996-04, Vol.134 (4), p.710-714

1996

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Genetic control of autoantibody expression in autoimmune myasthenia gravis: role of the self-antigen and of HLA-linked loci

Genes and immunity, 2004-07, Vol.5 (5), p.398-404

2004

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The M98K variant of the OPTINEURIN (OPTN) gene modifies initial intraocular pressure in patients with primary open angle glaucoma

Journal of medical genetics, 2003-11, Vol.40 (11), p.842-844

2003

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A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco

Clinical genetics, 2002-10, Vol.62 (4), p.334-339

2002

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Age-dependent HLA genetic heterogeneity of type 1 insulin-dependent diabetes mellitus

The Journal of clinical investigation, 1992-12, Vol.90 (6), p.2242-2250

1992

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XMR is associated with the asynapsed segments of sex chromosomes in the XY body of mouse primary spermatocytes

Chromosoma, 2000-07, Vol.109 (4), p.259-265

2000

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Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open-angle glaucoma

Clinical genetics, 2001-09, Vol.60 (3), p.220-225

2001

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Association of the gene encoding the δ-subunit of the muscle acetylcholine receptor (CHRND) with acquired autoimmune myasthenia gravis

Genes and immunity, 2004-01, Vol.5 (1), p.80-83

2004

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European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups

Molecular medicine (Cambridge, Mass.), 2009-11, Vol.15 (11-12), p.371-383

2009

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Genetic analysis of immune dysfunction in non‐obese diabetic (NOD) mice: Mapping of a susceptibility locus close to the Bcl‐2 gene correlates with increased resistance of NOD T cells to apoptosis induction

European journal of immunology, 1994-02, Vol.24 (2), p.380-384

1994

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OP0203 A Family-Based Genome-Wide Association Study Reveals an Association of Spondyloarthritis with MAPK14

Annals of the rheumatic diseases, 2015-06, Vol.74 (Suppl 2), p.148-148

2015

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Resistance of T-cells to apoptosis in autoimmune diabetic (NOD) mice is increased early in life and is associated with dysregulated expression of Bcl-x

Diabetologia, 1998-02, Vol.41 (2), p.178-184

1998

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Genetic and physical mapping of a type 1 diabetes susceptibility gene (IDDM12) to a 100-kb phagemid artificial chromosome clone containing D2S72-CTLA4-D2S105 on chromosome 2q33

Diabetes (New York, N.Y.), 2000-03, Vol.49 (3), p.492-499

2000

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FRI0446 Direct estimate of hla-b27 and spondyloarthritis prevalence in the general population: results of the french gazel cohort

Annals of the rheumatic diseases, 2013-06, Vol.72 (Suppl 3), p.A526-A526

2013

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Involvement of Human Muscle Acetylcholine Receptor α-Subunit Gene (CHRNA) in Susceptibility to Myasthenia Gravis

Proceedings of the National Academy of Sciences - PNAS, 1994-05, Vol.91 (11), p.4668-4672

1994

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N-terminus cleavage of bcl-2 by a novel cellular non-ICE cysteine proteinase

Leukemia, 1998-09, Vol.12 (9), p.1467-1472

1998

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Meiotic sex chromosome inactivation in male mice with targeted disruptions of Xist

Journal of cell science, 2002-11, Vol.115 (Pt 21), p.4097-4105

2002

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Comparative analysis in cynomolgus macaque identifies a novel human MHC locus controlling platelet blood counts independently of BAK1

Recurrent Mutations in a Single Exon Encoding the Evolutionarily Conserved Olfactomedin-Homology Domain of TIGR in Familial Open-Angle Glaucoma

Linkage of HLA to myasthenia gravis and genetic heterogeneity depending on anti-titin antibodies

A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family

Genetic influences on the end-stage effector phase of arthritis

CYP1B1 mutations in French patients with early-onset primary open-angle glaucoma

Insulin-Dependent Diabetes Mellitus (IDDM) Is Associated with CTLA4 Polymorphisms in Multiple Ethnic Groups

Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes

Apoptosis as a mechanism of keratinocyte death in toxic epidermal necrolysis

Genetic control of autoantibody expression in autoimmune myasthenia gravis: role of the self-antigen and of HLA-linked loci

The M98K variant of the OPTINEURIN (OPTN) gene modifies initial intraocular pressure in patients with primary open angle glaucoma

A novel frameshift founder mutation in the cytochrome P450 1B1 (CYP1B1) gene is associated with primary congenital glaucoma in Morocco

Age-dependent HLA genetic heterogeneity of type 1 insulin-dependent diabetes mellitus

XMR is associated with the asynapsed segments of sex chromosomes in the XY body of mouse primary spermatocytes

Association of a single nucleotide polymorphism in the TIGR/MYOCILIN gene promoter with the severity of primary open-angle glaucoma

Association of the gene encoding the δ-subunit of the muscle acetylcholine receptor (CHRND) with acquired autoimmune myasthenia gravis

European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups

Genetic analysis of immune dysfunction in non‐obese diabetic (NOD) mice: Mapping of a susceptibility locus close to the Bcl‐2 gene correlates with increased resistance of NOD T cells to apoptosis induction

OP0203 A Family-Based Genome-Wide Association Study Reveals an Association of Spondyloarthritis with MAPK14

Resistance of T-cells to apoptosis in autoimmune diabetic (NOD) mice is increased early in life and is associated with dysregulated expression of Bcl-x

Genetic and physical mapping of a type 1 diabetes susceptibility gene (IDDM12) to a 100-kb phagemid artificial chromosome clone containing D2S72-CTLA4-D2S105 on chromosome 2q33

FRI0446 Direct estimate of hla-b27 and spondyloarthritis prevalence in the general population: results of the french gazel cohort

Involvement of Human Muscle Acetylcholine Receptor α-Subunit Gene (CHRNA) in Susceptibility to Myasthenia Gravis

N-terminus cleavage of bcl-2 by a novel cellular non-ICE cysteine proteinase

Meiotic sex chromosome inactivation in male mice with targeted disruptions of Xist

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