E Haan - Concepedia

Author

E Haan

Women's and Children's Hospital

Also Known As

E A Haan, E Haan, E. A. HAAN, E. A. Haan, E. A.Haan, E. Haan, EA Haan, Eric Haan, S. White

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Women's and Children's Hospital The University of Adelaide The University of Western Australia Austin Health Royal Children's Hospital

About

E Haan is an author at Women's and Children's Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	316
2	Molecular Genetics	2	2	43
3	Public Health	1	1	67
4	Epidemiology	1	1	67
5	Molecular Medicine	1	1	24

E Haan

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID Bregje W.M. van Bon, Bradley P. Coe, Raphael Bernier, Molecular Psychiatry Neurodevelopmental DisordersDevelopmental BiologyDyrk1a LeadSyndromic AutismGenetic Disorder	2015	206
Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes David F. Callen, Helen J. Eyre, M‐Y Yip, American Journal of Medical Genetics	1992	173
Fetal alcohol syndrome: a prospective national surveillance study Elizabeth Elliott, Janet M Payne, Anne Morris, Archives of Disease in Childhood	2007	130
Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer--Giedion syndrome H.-J. Lüdecke, M.J. Wagner, J. Nardmann, Human Molecular Genetics	1995	123
Epilepsy and mental retardation limited to females with <i>PCDH19</i> mutations can present de novo or in single generation families Kim Hynes, Patrick Tarpey, Leanne M. Dibbens, Journal of Medical Genetics	2009	79
A South Australian population‐based study of congenital talipes equinovarus Rosemary Byron‐Scott, Phillipa Sharpe, Carol Hasler, Paediatric and Perinatal Epidemiology FertilityIsolated CtevReproductive HealthWildlife BiologyHigh-risk Pregnancy	2005	67
Fetal exposure to herpesviruses may be associated with pregnancy‐induced hypertensive disorders and preterm birth in a Caucasian population* C.F. Gibson, P N Goldwater, AH MacLennan, BJOG An International Journal of Obstetrics & Gynaecology	2008	66
FMR2 Expression in Families with Fraxe Mental Retardation Jozef Gécz, B. A. Oostra, Athel Hockey, Human Molecular Genetics	1997	61
Linkage studies with the gene for an X‐linked syndrome of mental retardation, microcephaly and spastic diplegia (MRX2) G.R. Sutherland, Ági K. Gedeon, E Haan, American Journal of Medical Genetics	1988	58
A maternal serum screen for trisomy 18: an extension of maternal serum screening for Down syndrome. A J Staples, E. F. Robertson, Enzo Ranieri, PubMed	1991	48

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