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Genetic linkage analysis in the age of whole-genome sequencing

Nature reviews. Genetics, 2015-05, Vol.16 (5), p.275-284

2015

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The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

Nature genetics, 2005-09, Vol.37 (9), p.931-933

2005

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HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families

Journal of human genetics, 2016-11, Vol.61 (11), p.959-963

2016

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Family-based designs for genome-wide association studies

Nature reviews. Genetics, 2011-07, Vol.12 (7), p.465-474

2011

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Beyond Homozygosity Mapping: Family-Control analysis based on Hamming distance for prioritizing variants in exome sequencing

Scientific reports, 2015-07, Vol.5 (1), p.12028-12028, Article 12028

2015

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A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q

Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie, 2020-11, Vol.48 (6), p.478-489

2020

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Coordinated Conditional Simulation with SLINK and SUP of Many Markers Linked or Associated to a Trait in Large Pedigrees

Human heredity, 2011-01, Vol.71 (2), p.126-134

2011

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Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR

Human genetics, 2005-12, Vol.118 (3-4), p.466-476

2005

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Writings on Genetic Linkage in the Annals

Annals of human genetics, 2011-05, Vol.75 (3), p.344-347

Ott, Jurg

2011

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Dysfunctional nitric oxide signalling increases risk of myocardial infarction

Nature (London), 2013-12, Vol.504 (7480), p.432-436

2013

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A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

Nature genetics, 1996-04, Vol.12 (4), p.431-435

1996

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Strategies for characterizing highly polymorphic markers in human gene mapping

American journal of human genetics, 1992-08, Vol.51 (2), p.283-290

OTT, J

1992

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Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata

American journal of human genetics, 2007-02, Vol.80 (2), p.316-328

2007

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Chromosomes 4q28.3 and 7q31.2 as New Susceptibility Loci for Comitant Strabismus

Investigative ophthalmology & visual science, 2009-02, Vol.50 (2), p.654-661

2009

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Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion: Evidence from Inherited Hypotrichosis and Acquired Pemphigus Vulgaris

Cell, 2003-04, Vol.113 (2), p.249-260

2003

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Combining identity by descent and association in genetic case-control studies

BMC genetics, 2008-07, Vol.9 (1), p.42, Article 42

2008

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Alopecia Universalis Associated with a Mutation in the Human Hairless Gene

Science (American Association for the Advancement of Science), 1998-01, Vol.279 (5351), p.720-724

1998

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PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Nature genetics, 2015-06, Vol.47 (6), p.647-653

2015

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Cold-Induced Sweating Syndrome Is Caused by Mutations in the CRLF1 Gene

American journal of human genetics, 2003-02, Vol.72 (2), p.375-383

2003

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Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22–Xp11.3

Genomics (San Diego, Calif.), 1991-05, Vol.10 (1), p.29-33

1991

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Significant Linkage for Tourette Syndrome in a Large French Canadian Family

American journal of human genetics, 2000-10, Vol.67 (4), p.1008-1013

2000

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Expanded Genome Scan in Extended Families with Age-Related Macular Degeneration

Investigative ophthalmology & visual science, 2006-12, Vol.47 (12), p.5453-5459

2006

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A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3

Nature genetics, 1994-11, Vol.8 (3), p.291-296

1994

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Familial Juvenile Hyperuricemic Nephropathy: Localization of the Gene on Chromosome 16p11.2—and Evidence for Genetic Heterogeneity

American journal of human genetics, 2000-06, Vol.66 (6), p.1989-1994

2000

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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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Genetic linkage analysis in the age of whole-genome sequencing

The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia

HDR: a statistical two-step approach successfully identifies disease genes in autosomal recessive families

Family-based designs for genome-wide association studies

Beyond Homozygosity Mapping: Family-Control analysis based on Hamming distance for prioritizing variants in exome sequencing

A Novel Locus and Candidate Gene for Familial Developmental Dyslexia on Chromosome 4q

Coordinated Conditional Simulation with SLINK and SUP of Many Markers Linked or Associated to a Trait in Large Pedigrees

Localization of PSORS1 to a haplotype block harboring HLA-C and distinct from corneodesmosin and HCR

Writings on Genetic Linkage in the Annals

Dysfunctional nitric oxide signalling increases risk of myocardial infarction

A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish

Strategies for characterizing highly polymorphic markers in human gene mapping

Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata

Chromosomes 4q28.3 and 7q31.2 as New Susceptibility Loci for Comitant Strabismus

Desmoglein 4 in Hair Follicle Differentiation and Epidermal Adhesion: Evidence from Inherited Hypotrichosis and Acquired Pemphigus Vulgaris

Combining identity by descent and association in genetic case-control studies

Alopecia Universalis Associated with a Mutation in the Human Hairless Gene

PDE3A mutations cause autosomal dominant hypertension with brachydactyly

Cold-Induced Sweating Syndrome Is Caused by Mutations in the CRLF1 Gene

Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22–Xp11.3

Significant Linkage for Tourette Syndrome in a Large French Canadian Family

Expanded Genome Scan in Extended Families with Age-Related Macular Degeneration

A possible vulnerability locus for bipolar affective disorder on chromosome 21q22.3

Familial Juvenile Hyperuricemic Nephropathy: Localization of the Gene on Chromosome 16p11.2—and Evidence for Genetic Heterogeneity

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

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