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Eric A. Haan

Eric A. Haan,University of Adelaide,Genetics & Genealogy,Gynecology & Obstetrics,Family Medicine

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Eric A. Haan

University of Adelaide

Publications: 173 | Citations: 3296

Fields: Genetics & Genealogy, Gynecology & Obstetrics, Family Medicine

Collaborated with 1039 co-authors from 1979 to 2011 | Cited by 14155 authors

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Publications (173)

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Lung disease associated with periventricular nodular heterotopia and an FLNA mutation (Citations: 1)

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Journal: European Journal of Medical Genetics - EUR J MED GENET , vol. 54, no. 1, pp. 25-28, 2011

The australian cerebral palsy research study – epidemiological and genetic associations with cerebral palsy

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Journal: Archives of Disease in Childhood-fetal and Neonatal Edition - ARCH DIS CHILD-FETAL NEONATAL , vol. 96, no. 1, pp. Fa15-Fa16, 2011

TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families

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Journal: Orphanet Journal of Rare Diseases - ORPHANET J RARE DIS , vol. 6, no. 1, pp. 1-8, 2011

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay (Citations: 49)

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Journal: Nature Genetics - NAT GENET , vol. 42, no. 3, pp. 203-209, 2010

Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families (Citations: 5)

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Journal: Journal of Medical Genetics - J MED GENET , vol. 47, no. 3, pp. 211-216, 2010

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Citations (3296 times by 3065 publications)

Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

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Journal: PLOS One , vol. 7, no. 6, 2012

Pooled Sample-Based GWAS: A Cost-Effective Alternative for Identifying Colorectal and Prostate Cancer Risk Variants in the Polish Population

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Journal: PLOS One , vol. 7, no. 4, 2012

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Co-authors (1039)

Journals (57)

Keywords (246)

Eric A. Haan,University of Adelaide,Genetics & Genealogy,Gynecology & Obstetrics,Family Medicine

Publications (173)

BibTeX | RIS | RefWorks Download

Lung disease associated with periventricular nodular heterotopia and an FLNA mutation (Citations: 1)

The australian cerebral palsy research study – epidemiological and genetic associations with cerebral palsy

TRPV4 related skeletal dysplasias: a phenotypic spectrum highlighted byclinical, radiographic, and molecular studies in 21 new families

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay (Citations: 49)

Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families (Citations: 5)

Citations (3296 times by 3065 publications)

Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

Genome-Wide Copy Number Analysis Uncovers a New HSCR Gene: NRG3

Quantitative Assessment of Whole-Body Tumor Burden in Adult Patients with Neurofibromatosis

Pooled Sample-Based GWAS: A Cost-Effective Alternative for Identifying Colorectal and Prostate Cancer Risk Variants in the Polish Population


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Eric A. Haan,University of Adelaide,Genetics & Genealogy,Gynecology & Obstetrics,Family Medicine

Publications (173) BibTeX | RIS | RefWorks Download

Lung disease associated with periventricular nodular heterotopia and an FLNA mutation (Citations: 1)

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay (Citations: 49)

Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families (Citations: 5)

Publications (173)

BibTeX | RIS | RefWorks Download