M. Blundell

发表

The mutational status of p53 protein in gastric and esophageal adenocarcinoma cell lines predicts sensitivity to chemotherapeutic agents

P. Maslak, N. Altorki, G. Schwartz, 1995, International journal of cancer.

Early, non-psychotic deviant behavior in schizophrenia: a possible endophenotypic marker for genetic studies

M. Karayiorgou, C. Sobin, M. Blundell, 2001, Psychiatry Research.

Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q

E. Wijsman, S. Heath, M. Karayiorgou, 2003, Molecular Psychiatry.

Acidic fibroblast growth factor is progressively increased in the development of oesophageal glandular dysplasia and adenocarcinoma

Y. Nabeya, M. Blundell, R. Soslow, 1999, Histopathology.

Loss of heterozygosity and homozygous deletion of the tpr locus in human gastric cancer.

S. Jhanwar, G. Schwartz, A. Albino, 1997, American journal of surgery.

Amplification of HER-2/neu gene in human gastric adenocarcinomas: correlation with primary site.

N. Altorki, D. Niedzwiecki, A. Albino, 1995, European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology.

Genome-Wide Association Studies in an Isolated Founder Population from the Pacific Island of Kosrae

Benjamin M. Neale, Itsik Pe'er, Julian B. Maller, 2009, PLoS genetics.

Phytosterolemia on the island of Kosrae: founder effect for a novel ABCG8 mutation results in high carrier rate and increased plasma plant sterol levels.

M. Stoffel, J. Salit, M. Blundell, 2004, Journal of lipid research.

Evidence of a schizotypy subtype in OCD.

M. Karayiorgou, C. Sobin, M. Blundell, 2000, Journal of psychiatric research.

Candidate genes involved in cardiovascular risk factors by a family-based association study on the island of Kosrae, Federated States of Micronesia.

Wentian Li, J. Ott, S. Heath, 2002, American journal of medical genetics.

Characterization of cell lines established from human gastric‐esophageal adenocarcinomas: Biologic phenotype and invasion potential

N. Altorki, G. Schwartz, A. Albino, 1993, Cancer.

Homozygosity mapping of the Achromatopsia locus in the Pingelapese.

S. Leal, M. Karayiorgou, M. Blundell, 1999, American journal of human genetics.

Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophrenia

Ellen M Wijsman, Christina Sobin, Maria Karayiorgou, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Family-based association studies support a sexually dimorphic effect of COMT and MAOA on genetic susceptibility to obsessive-compulsive disorder

Jurg Ott, Joseph A. Gogos, Christina Sobin, 1999, Biological Psychiatry.

Genome-Wide Association Studies in an Isolated Founder Population from the Pacific Island of Kosrae Citation Lowe

M. Daly, D. Altshuler, B. Neale, 2009 .

Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance

W. Foulkes, C. Hawkins, G. Nicholas, 2021, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Linkage analysis of quantitative traits for obesity, diabetes, hypertension, and dyslipidemia on the island of Kosrae, Federated States of Micronesia.

S. Heath, M. Stoffel, J. Salit, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Phenotypic characterization and genealogical tracing in an Afrikaner schizophrenia database

G. Abecasis, M. Karayiorgou, S. L. Lundy, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Epidemiology and Factor Analysis of Obesity, Type II Diabetes, Hypertension, and Dyslipidemia (Syndrome X) on the Island of Kosrae, Federated States of Micronesia

Thomas Lehner, J. Ott, S. Heath, 2000, Human Heredity.

Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q

E. Wijsman, S. Heath, M. Karayiorgou, 2003, Molecular Psychiatry.

Networks of Attention in Children With the 22q11 Deletion Syndrome

Christina Sobin, Sarah Daniels, Maria Karayiorgou, 2004, Developmental neuropsychology.

Phenotypic characteristics of Obsessive-Compulsive Disorder ascertained in adulthood.

M. Karayiorgou, C. Sobin, M. Blundell, 1999, Journal of psychiatric research.

Phenotypic differences in early- and late-onset obsessive-compulsive disorder.

M. Karayiorgou, C. Sobin, M. Blundell, 2000, Comprehensive psychiatry.

NEUROPSYCHOLOGICAL CHARACTERISTICS OF CHILDREN WITH THE 22Q11 DELETION SYNDROME: A DESCRIPTIVE ANALYSIS

M. Karayiorgou, C. Sobin, M. Blundell, 2005, Child neuropsychology : a journal on normal and abnormal development in childhood and adolescence.

Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study.

K. Cole, D. Gass, A. Shlien, 2024, The Lancet. Oncology.