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Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome

Nature genetics, 2011-04, Vol.43 (4), p.360-364

2011

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Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4

American journal of human genetics, 2010-07, Vol.87 (1), p.40-51

2010

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Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia

Nature genetics, 2009-06, Vol.41 (6), p.651-653

2009

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Mutation in the gene encoding ubiquitin ligase LRSAM1 in patients with Charcot-Marie-Tooth disease

PLoS genetics, 2010-08, Vol.6 (8), p.e1001081

2010

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Neosis: A Novel Type of Cell Division in Cancer

Cancer biology & therapy, 2004-02, Vol.3 (2), p.207-218

2004

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Stem cells, senescence, neosis and self-renewal in cancer

Cancer cell international, 2006-11, Vol.6 (1), p.25-25

2006

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Polymorphisms in DNA repair genes in the molecular pathogenesis of esophageal (Barrett) adenocarcinoma

Carcinogenesis (New York), 2005-09, Vol.26 (9), p.1536-1541

2005

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Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data

PloS one, 2009-04, Vol.4 (4), p.e5280-e5280

2009

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Regulation of CDX2 expression in esophageal adenocarcinoma

Molecular carcinogenesis, 2009-10, Vol.48 (10), p.965-974

2009

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Inducible nitric oxide synthase, nitrotyrosine and p53 mutations in the molecular pathogenesis of Barrett's esophagus and esophageal adenocarcinoma

Molecular carcinogenesis, 2008-04, Vol.47 (4), p.275-285

2008

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Loss of adenylyl cyclase I activity disrupts patterning of mouse somatosensory cortex

Nature genetics, 1998-07, Vol.19 (3), p.289-291

1998

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Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

Nature genetics, 2002-10, Vol.32 (2), p.326-330

2002

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Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2

American journal of human genetics, 2009-07, Vol.85 (1), p.120-129

2009

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The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease

British journal of ophthalmology, 2011-04, Vol.95 (4), p.574-579

2011

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Neosis – a paradigm of self-renewal in cancer

Cell biology international, 2005-12, Vol.29 (12), p.1084-1097

2005

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Mutations in a novel serine protease PRSS56 in families with nanophthalmos

Molecular vision, 2011, Vol.17, p.1850-1861

2011

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Severe retinopathy of prematurity associated with FZD4 mutations

Ophthalmic genetics, 2010-03, Vol.31 (1), p.37-43

2010

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A polymorphic variant of the insulin-like growth factor type I receptor gene modifies risk of obesity for esophageal adenocarcinoma

Cancer epidemiology, 2009-07, Vol.33 (1), p.37-40

2009

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Phenotypic Overlap of Familial Exudative Vitreoretinopathy (FEVR) with Persistent Fetal Vasculature (PFV) Caused by FZD4 Mutations in two Distinct Pedigrees

Ophthalmic genetics, 2009-03, Vol.30 (1), p.23-30

2009

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Genetic polymorphisms of microsomal epoxide hydroxylase and glutathione S-transferases M1, T1 and P1, interactions with smoking, and risk for esophageal (Barrett) adenocarcinoma

Cancer detection and prevention, 2006-01, Vol.30 (5), p.423-431

2006

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Cyclin D1 polymorphism (G870A) and risk for esophageal adenocarcinoma

Cancer, 2005-08, Vol.104 (4), p.730-739

2005

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Current and future approaches for the therapeutic targeting of metastasis (Review)

International journal of molecular medicine, 2006-12, Vol.18 (6), p.1025-1036

2006

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Clinical implications of p53 tumor suppressor gene mutation and protein expression in esophageal adenocarcinomas: Results of a ten-year prospective study

The Journal of thoracic and cardiovascular surgery, 2003-05, Vol.125 (5), p.1121-1131

2003

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Is gene discovery research or diagnosis?

Genetics in medicine, 2008-06, Vol.10 (6), p.385-390

2008

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Epidemiology and Molecular Biology of Barrett Esophagus

Seminars in thoracic and cardiovascular surgery, 2005-12, Vol.17 (4), p.284-291, Article 284

2005

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Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome

Mutations in Centrosomal Protein CEP152 in Primary Microcephaly Families Linked to MCPH4

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia

Mutation in the gene encoding ubiquitin ligase LRSAM1 in patients with Charcot-Marie-Tooth disease

Neosis: A Novel Type of Cell Division in Cancer

Stem cells, senescence, neosis and self-renewal in cancer

Polymorphisms in DNA repair genes in the molecular pathogenesis of esophageal (Barrett) adenocarcinoma

Application of homozygosity haplotype analysis to genetic mapping with high-density SNP genotype data

Regulation of CDX2 expression in esophageal adenocarcinoma

Inducible nitric oxide synthase, nitrotyrosine and p53 mutations in the molecular pathogenesis of Barrett's esophagus and esophageal adenocarcinoma

Loss of adenylyl cyclase I activity disrupts patterning of mouse somatosensory cortex

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

Mutation in Pyrroline-5-Carboxylate Reductase 1 Gene in Families with Cutis Laxa Type 2

The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease

Neosis – a paradigm of self-renewal in cancer

Mutations in a novel serine protease PRSS56 in families with nanophthalmos

Severe retinopathy of prematurity associated with FZD4 mutations

A polymorphic variant of the insulin-like growth factor type I receptor gene modifies risk of obesity for esophageal adenocarcinoma

Phenotypic Overlap of Familial Exudative Vitreoretinopathy (FEVR) with Persistent Fetal Vasculature (PFV) Caused by FZD4 Mutations in two Distinct Pedigrees

Genetic polymorphisms of microsomal epoxide hydroxylase and glutathione S-transferases M1, T1 and P1, interactions with smoking, and risk for esophageal (Barrett) adenocarcinoma

Cyclin D1 polymorphism (G870A) and risk for esophageal adenocarcinoma

Current and future approaches for the therapeutic targeting of metastasis (Review)

Clinical implications of p53 tumor suppressor gene mutation and protein expression in esophageal adenocarcinomas: Results of a ten-year prospective study

Is gene discovery research or diagnosis?

Epidemiology and Molecular Biology of Barrett Esophagus

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