William Hennah - Concepedia

Author

William Hennah

Institute for Molecular Medicine Finland ORCID

Also Known As

E Ghiban, Hennah, William, Varilo, Teppo, W Hennah, W. HENNAH, W. Hennah, William Hennah

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Institute for Molecular Medicine Finland University of Helsinki Helsinki University Hospital Finnish Institute for Health and Welfare Finnish Foundation for Alcohol Studies

About

William Hennah is an author at Institute for Molecular Medicine Finland specializing in medicine, psychiatry, and schizophrenia.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	19	1.9K
2	Social Sciences	8	8	800
3	Public Health	3	3	391
4	Biostatistics	2	2	76
5	Cell Biology	1	1	17

William Hennah

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
Association of DISC1/TRAX Haplotypes With Schizophrenia, Reduced Prefrontal Gray Matter, and Impaired Short- and Long-term Memory Tyrone D. Cannon, William Hennah, Theo G.M. van Erp, Archives of General Psychiatry	2005	341
Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects William Hennah Human Molecular Genetics GeneticsGenetic EpidemiologyHuman PolymorphismNeuropsychiatryFinnish Schizophrenia Sample	2003	328
Specific developmental disruption of disrupted-in-schizophrenia-1 function results in schizophrenia-related phenotypes in mice Weidong Li, Yu Zhou, J. David Jentsch, Proceedings of the National Academy of Sciences NeuropsychologyBrain FunctionBrain DevelopmentGeneticsSchizophrenia-related Phenotypes	2007	208
Association of DISC1 with autism and Asperger syndrome Helena Kilpinen, Tero Ylisaukko‐oja, William Hennah, Molecular Psychiatry Neurodevelopmental DisordersPsychiatrySyndromic AutismAutismNeuropathology	2007	192
Replication of 1q42 linkage in Finnish schizophrenia pedigrees Jesper Ekelund, William Hennah, Tero Hiekkalinna, Molecular Psychiatry PsychiatryGenetic DisorderGeneticsPsychiatric GeneticsGenetic Epidemiology	2004	185
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders Georg Stoll, Olli Pietiläinen, Bastian Linder, Nature Neuroscience Neurodevelopmental DisordersFmrp-containing MrnpsDevelopmental BiologyMolecular NeuroscienceBrain Development	2013	172
DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder William Hennah, Pippa A. Thomson, Andrew McQuillin, Molecular Psychiatry PsychopathologyDisc1 AssociationPsychiatryPsychotic DisorderSchizophrenia	2008	163
A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia William Hennah, Annamari Tuulio‐Henriksson, Tiina Paunio, Molecular Psychiatry High DensityPsychiatryBrain FunctionMedicinePsychotic Disorder	2005	157
Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments Outi M. Palo, M. Antila, Kaisa Silander, Human Molecular Genetics	2007	131
Association Between Genes of Disrupted in Schizophrenia 1 (DISC1) Interactors and Schizophrenia Supports the Role of the DISC1 Pathway in the Etiology of Major Mental Illnesses Liisa Tomppo, William Hennah, Päivi Lahermo, Biological Psychiatry Major Mental IllnessesPsychiatrySchizophrenia 1GeneticsPsychiatric Genetics	2009	86

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