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Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample

PloS one, 2016-04, Vol.11 (4), p.e0152984

2016

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Investigation of promoter variations in dendritic cell-specific ICAM3-grabbing non-integrin (DC-SIGN) (CD209) and their relevance for human cytomegalovirus reactivation and disease after allogeneic stem-cell transplantation

Clinical microbiology and infection, 2008-03, Vol.14 (3), p.228-234

2008

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German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2

Diabetologia, 2007-07, Vol.50 (7), p.1418-1422

2007

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Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy

American journal of human genetics, 2002-02, Vol.70 (2), p.358-368

2002

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Genome search for susceptibility loci of common idiopathic generalised epilepsies

Human molecular genetics, 2000-06, Vol.9 (10), p.1465-1472

2000

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Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients

Journal of medical genetics, 2006-06, Vol.43 (6), p.517-522

2006

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β-2 Adrenoceptor genetic variation is associated with genetic predisposition to essential hypertension: The Bergen Blood Pressure Study

Kidney international, 1998-06, Vol.53 (6), p.1455-1460

1998

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Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasis

British journal of dermatology (1951), 2003-08, Vol.149 (2), p.381-385

2003

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Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

Neurology, 1997-09, Vol.49 (3), p.842

1997

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A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26

Molecular psychiatry, 2001-05, Vol.6 (3), p.342-349

2001

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Linkage of the Gene for the Triple A Syndrome to Chromosome 12q13 Near the Type II Keratin Gene Cluster

Human molecular genetics, 1996-12, Vol.5 (12), p.2061-2066

1996

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Investigation of a Family with Autosomal Dominant Dilated Cardiomyopathy Defines a Novel Locus on Chromosome 2q14-q22

American journal of human genetics, 1999-10, Vol.65 (4), p.1068-1077

1999

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Pharmacogenetics of clozapine response

The Lancet (British edition), 2000-08, Vol.356 (9228), p.506-507

2000

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Diaphragmatic Spinal Muscular Atrophy with Respiratory Distress Is Heterogeneous, and One Form Is Linked to Chromosome 11q13-q21

American journal of human genetics, 1999-11, Vol.65 (5), p.1459-1462

1999

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Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective loci

Experimental dermatology, 2003-08, Vol.12 (4), p.490-496

2003

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Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12

Nature genetics, 1996-05, Vol.13 (1), p.98-100

1996

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The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21

American journal of human genetics, 1997-03, Vol.60 (3), p.605-610

1997

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Exclusion of the neuronal nicotinic acetylcholine receptor α7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus

Molecular psychiatry, 2002-02, Vol.7 (2), p.220-223

2002

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Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27

American journal of human genetics, 1999-02, Vol.64 (2), p.538-546

1999

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Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1

Journal of medical genetics, 2009-11, Vol.46 (11), p.736-744

2009

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On the genetics of mandibular prognathism: analysis of large European noble families

Journal of medical genetics, 1993-02, Vol.30 (2), p.112-116

1993

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Localization of a Gene for Syndactyly Type 1 to Chromosome 2q34-q36

American journal of human genetics, 2000-08, Vol.67 (2), p.492-497

2000

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Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism

American journal of medical genetics, 1997-07, Vol.74 (4), p.416-421

1997

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Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly

Stroke (1970), 1997-09, Vol.28 (9), p.1749-1754

1997

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Autosomal Dominant Hypertension and Brachydactyly in a Turkish Kindred Resembles Essential Hypertension

Hypertension (Dallas, Tex. 1979), 1996-12, Vol.28 (6), p.1085-1092

1996

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Association of Common Polymorphisms in the Nicotinic Acetylcholine Receptor Alpha4 Subunit Gene with an Electrophysiological Endophenotype in a Large Population-Based Sample

Investigation of promoter variations in dendritic cell-specific ICAM3-grabbing non-integrin (DC-SIGN) (CD209) and their relevance for human cytomegalovirus reactivation and disease after allogeneic stem-cell transplantation

German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2

Quantitative Analyses of SMN1 and SMN2 Based on Real-Time LightCycler PCR: Fast and Highly Reliable Carrier Testing and Prediction of Severity of Spinal Muscular Atrophy

Genome search for susceptibility loci of common idiopathic generalised epilepsies

Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients

β-2 Adrenoceptor genetic variation is associated with genetic predisposition to essential hypertension: The Bergen Blood Pressure Study

Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasis

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25-q26

Linkage of the Gene for the Triple A Syndrome to Chromosome 12q13 Near the Type II Keratin Gene Cluster

Investigation of a Family with Autosomal Dominant Dilated Cardiomyopathy Defines a Novel Locus on Chromosome 2q14-q22

Pharmacogenetics of clozapine response

Diaphragmatic Spinal Muscular Atrophy with Respiratory Distress Is Heterogeneous, and One Form Is Linked to Chromosome 11q13-q21

Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective loci

Severe autosomal dominant hypertension and brachydactyly in a unique Turkish kindred maps to human chromosome 12

The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21

Exclusion of the neuronal nicotinic acetylcholine receptor α7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus

Limb Mammary Syndrome: A New Genetic Disorder with Mammary Hypoplasia, Ectrodactyly, and Other Hand/Foot Anomalies Maps to Human Chromosome 3q27

Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1

On the genetics of mandibular prognathism: analysis of large European noble families

Localization of a Gene for Syndactyly Type 1 to Chromosome 2q34-q36

Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism

Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly

Autosomal Dominant Hypertension and Brachydactyly in a Turkish Kindred Resembles Essential Hypertension

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