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Validating, augmenting and refining genome-wide association signals

Nature reviews. Genetics, 2009-05, Vol.10 (5), p.318-329

2009

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Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse

Nature genetics, 1999-02, Vol.21 (2), p.195-199

1999

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Requirement for Wnt3 in vertebrate axis formation

Nature genetics, 1999-08, Vol.22 (4), p.361-365

1999

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Rapid gene mapping in Caenorhabditis elegans using a high density polymorphism map

Nature genetics, , Vol.28 (2), p.160-164

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Vertebrate genome evolution and the zebrafish gene map

Nature genetics, 1998-04, Vol.18 (4), p.345-349

1998

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Trends in large-scale mouse mutagenesis: from genetics to functional genomics

Nature reviews. Genetics, 2008-10, Vol.9 (10), p.803-810

Gondo, Yoichi

2008

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ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

Nature genetics, 2004-04, Vol.36 (4), p.382-387

2004

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Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

Nature genetics, 2001-07, Vol.28 (3), p.223-231

2001

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A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase

Nature genetics, 1998-02, Vol.18 (2), p.159-163

1998

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Sox9 expression during gonadal development implies a conserved role for the gene in testis differentiation in mammals and birds

Nature genetics, 1996-09, Vol.14 (1), p.62-68

1996

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Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3

Nature genetics, 1996-04, Vol.12 (4), p.390-397

1996

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Abnormal lung development and cleft palate in mice lacking TGF-β3 indicates defects of epithelial-mesenchymal interaction

Nature genetics, 1995-12, Vol.11 (4), p.415-421

1995

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Human DF3 MUC1 carcinoma-associated protein functions as an oncogene

Oncogene, 2003-09, Vol.22 (38), p.6107-6110

2003

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Transforming growth factor-β3 is required for secondary palate fusion

Nature genetics, 1995-12, Vol.11 (4), p.409-414

1995

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X-linked situs abnormalities result from mutations in ZIC3

Nature genetics, 1997-11, Vol.17 (3), p.305-308

1997

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Absence of integrin α7 causes a novel form of muscular dystrophy

Nature genetics, 1997-11, Vol.17 (3), p.318-323

1997

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Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy

European journal of human genetics : EJHG, 2010-06, Vol.18 (6), p.700-706

2010

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The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

Nature genetics, 1999-04, Vol.21 (4), p.434-439

1999

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Mitochondrial DNA genotypes in nuclear transfer-derived cloned sheep

Nature genetics, 1999-09, Vol.23 (1), p.90-93

1999

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Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

Nature genetics, 1994-04, Vol.6 (4), p.348-356

1994

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A mouse model for hereditary thyroid dysgenesis and cleft palate

Nature genetics, 1998-08, Vol.19 (4), p.395-398

1998

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Loss of Gcn512 leads to increased apoptosis and mesodermal defects during mouse development

Nature genetics, 2000-10, Vol.26 (2), p.229-232

2000

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Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis

Nature genetics, 1995-09, Vol.11 (1), p.40-44

1995

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The evolutionary history of Drosophila buzzatii. XXXIII. Are Opuntia hosts a selective factor for the inversion polymorphism?

Heredity, 1996-11, Vol.77 (5), p.500-508

1996

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Validating, augmenting and refining genome-wide association signals

Hephaestin, a ceruloplasmin homologue implicated in intestinal iron transport, is defective in the sla mouse

Requirement for Wnt3 in vertebrate axis formation

Rapid gene mapping in Caenorhabditis elegans using a high density polymorphism map

Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis

Vertebrate genome evolution and the zebrafish gene map

Trends in large-scale mouse mutagenesis: from genetics to functional genomics

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria

A novel neurological phenotype in mice lacking mitochondrial manganese superoxide dismutase

Sox9 expression during gonadal development implies a conserved role for the gene in testis differentiation in mammals and birds

Skeletal overgrowth and deafness in mice lacking fibroblast growth factor receptor 3

Abnormal lung development and cleft palate in mice lacking TGF-β3 indicates defects of epithelial-mesenchymal interaction

Human DF3 MUC1 carcinoma-associated protein functions as an oncogene

Transforming growth factor-β3 is required for secondary palate fusion

X-linked situs abnormalities result from mutations in ZIC3

Absence of integrin α7 causes a novel form of muscular dystrophy

Meta-analysis of 20 genome-wide linkage studies evidenced new regions linked to asthma and atopy

The gene encoding proline dehydrogenase modulates sensorimotor gating in mice

Mitochondrial DNA genotypes in nuclear transfer-derived cloned sheep

Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

A mouse model for hereditary thyroid dysgenesis and cleft palate

Loss of Gcn512 leads to increased apoptosis and mesodermal defects during mouse development

Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis

The evolutionary history of Drosophila buzzatii. XXXIII. Are Opuntia hosts a selective factor for the inversion polymorphism?

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