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Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A

Leukemia, 2014-05, Vol.28 (5), p.1136-1138

2014

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Molecular karyotyping using an SNP array for genomewide genotyping

Journal of medical genetics, 2004-12, Vol.41 (12), p.916-922

2004

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Missense mutations of ACTA1 cause dominant congenital myopathy with cores

Journal of medical genetics, 2004-11, Vol.41 (11), p.842-848

2004

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A major susceptibility locus for atopic dermatitis maps to chromosome 3q21

Nature genetics, 2000-12, Vol.26 (4), p.470-473

2000

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ALOHOMORA: a tool for linkage analysis using 10K SNP array data

Bioinformatics, 2005-05, Vol.21 (9), p.2123-2125

2005

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Genomewide Scan in German Families Reveals Evidence for a Novel Psoriasis-Susceptibility Locus on Chromosome 19p13

American journal of human genetics, 2000-10, Vol.67 (4), p.1020-1024

2000

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Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march

Journal of allergy and clinical immunology, 2006-10, Vol.118 (4), p.866-871

2006

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A genome‐wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3

Allergy (Copenhagen), 2005-02, Vol.60 (2), p.192-199

2005

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Identification of a New Gene Locus for Adolescent Nephronophthisis, on Chromosome 3q22 in a Large Venezuelan Pedigree

American journal of human genetics, 2000-01, Vol.66 (1), p.118-127

2000

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Divergent genetic and epigenetic post‐zygotic isolation mechanisms in Mus and Peromyscus

Journal of evolutionary biology, 2004-03, Vol.17 (2), p.453-460

2004

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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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Refinement of the Gene Locus for Autosomal Dominant Medullary Cystic Kidney Disease Type 1 (MCKD1) and Construction of a Physical and Partial Transcriptional Map of the Region

Genomics (San Diego, Calif.), 2001-03, Vol.72 (3), p.278-284

2001

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Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes

Human mutation, 2001-10, Vol.18 (4), p.327-336

2001

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A second large family with catatonic schizophrenia supports the region distally of CHRNA7 on chromosome 15q14-15

Molecular psychiatry, 2003-03, Vol.8 (3), p.259-260

2003

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781 SMARCAD1 haploinsufficiency underlies Huriez Syndrome and associated skin cancer susceptibility

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S133-S133

2018

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Genetic Dissection of X-Linked Interspecific Hybrid Placental Dysplasia in Congenic Mouse Strains

Genetics (Austin), 1999-09, Vol.153 (1), p.383-390

1999

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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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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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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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Murine susceptibility to Chagas' disease maps to chromosomes 5 and 17

Genes and immunity, 2003-07, Vol.4 (5), p.321-325

2003

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Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15

American journal of human genetics, 2000-11, Vol.67 (5), p.1201-1207

2000

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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

2002

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Mutations in MRAP , encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

Nature genetics, 2005-02, Vol.37 (2), p.166-170

2005

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Eleven loci with new reproducible genetic associations with allergic disease risk

Journal of allergy and clinical immunology, 2019-02, Vol.143 (2), p.691-699

2019

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Promoter Polymorphism at –238 of the Tumor Necrosis Factor Alpha Gene is Not Associated with Early Onset Psoriasis when Tested by the Transmission Disequilibrium Test

Journal of investigative dermatology, 1999-04, Vol.112 (4), p.514-515

1999

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Inherited susceptibility to pre B-ALL caused by germline transmission of PAX5 c.547G>A

Molecular karyotyping using an SNP array for genomewide genotyping

Missense mutations of ACTA1 cause dominant congenital myopathy with cores

A major susceptibility locus for atopic dermatitis maps to chromosome 3q21

ALOHOMORA: a tool for linkage analysis using 10K SNP array data

Genomewide Scan in German Families Reveals Evidence for a Novel Psoriasis-Susceptibility Locus on Chromosome 19p13

Filaggrin loss-of-function mutations predispose to phenotypes involved in the atopic march

A genome‐wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3

Identification of a New Gene Locus for Adolescent Nephronophthisis, on Chromosome 3q22 in a Large Venezuelan Pedigree

Divergent genetic and epigenetic post‐zygotic isolation mechanisms in Mus and Peromyscus

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

Refinement of the Gene Locus for Autosomal Dominant Medullary Cystic Kidney Disease Type 1 (MCKD1) and Construction of a Physical and Partial Transcriptional Map of the Region

Fine mapping and single nucleotide polymorphism association results of candidate genes for asthma and related phenotypes

A second large family with catatonic schizophrenia supports the region distally of CHRNA7 on chromosome 15q14-15

781 SMARCAD1 haploinsufficiency underlies Huriez Syndrome and associated skin cancer susceptibility

Genetic Dissection of X-Linked Interspecific Hybrid Placental Dysplasia in Congenic Mouse Strains

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

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

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

Murine susceptibility to Chagas' disease maps to chromosomes 5 and 17

Splitting Schizophrenia: Periodic Catatonia–Susceptibility Locus on Chromosome 15q15

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

Mutations in MRAP , encoding a new interacting partner of the ACTH receptor, cause familial glucocorticoid deficiency type 2

Eleven loci with new reproducible genetic associations with allergic disease risk

Promoter Polymorphism at –238 of the Tumor Necrosis Factor Alpha Gene is Not Associated with Early Onset Psoriasis when Tested by the Transmission Disequilibrium Test

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