Gerard D. Schellenberg

Author

Also Known As

Bruce L. Miller, Carlos Cruchaga, Carracedo, Ángel, Charles DeCarli, Claudia Satizabal, Cruchaga, Carlos, Daniel H. Geschwind, Dombroski, Beth, Eden Martin, Eden R. Martin

491

Publications

40.4K

Citations

H-Index

142

Concepts

All Affiliations

University of Washington University of Pennsylvania Geriatric Research Education and Clinical Center Boston University University of Miami

About

Gerard D. Schellenberg is an author at University of Washington specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	46	68	12.4K
2	Health Sciences	10	10	786
3	Natural Sciences	2	2	129
4	Education	1	1	136
5	Engineering	1	1	20

Gerard D. Schellenberg

209

Publications

35.3K

Citations

H-Index

Page 1

	Year	Citations
Candidate Gene for the Chromosome 1 Familial Alzheimer's Disease Locus Ephrat Levy‐Lahad, Wilma Wasco, Parvoneh Poorkaj, Science Alzheimer's DiseaseGenetic DisorderGeneticsMolecular BiologyPoint Mutation	1995	2.6K
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
Patterns and rates of exonic de novo mutations in autism spectrum disorders Benjamin M. Neale, Yan Kou, Li Liu, Nature Neurodevelopmental DisordersAutism Spectrum DisordersSyndromic AutismGeneticsGenetic Disorder	2012	1.8K
Positional Cloning of the Werner's Syndrome Gene Chang-En Yu, Junko Oshima, Ying‐Hui Fu, Science	1996	1.7K
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes Joseph Glessner, Kai Wang, Guiqing Cai, Nature	2009	1.4K
Tau is a candidate gene for chromosome 17 frontotemporal dementia Parvoneh Poorkaj, Thomas D. Bird, Ellen M. Wijsman, Annals of Neurology	1998	1.4K
A framework for the interpretation of de novo mutation in human disease Kaitlin E. Samocha, Elise Robinson, Stephan Sanders, Nature Genetics Somatic VariantGenetic DisorderMedicineGeneticsHuman Disease	2014	1.1K
Common genetic variants on 5p14.1 associate with autism spectrum disorders Kai Wang, Haitao Zhang, Deqiong Ma, Nature Neurodevelopmental DisordersSyndromic AutismGenetic DisorderGeneticsPsychiatric Genetics	2009	968
Genetic Linkage Evidence for a Familial Alzheimer's Disease Locus on Chromosome 14 Gerard D. Schellenberg, Thomas D. Bird, Ellen M. Wijsman, Science Neurodegenerative DiseasesDisease LocusAlzheimer's DiseaseGenetic DisorderGenetics	1992	943
Dementia and Alzheimer Disease Incidence Walter A. Kukull, Roger Higdon, James D. Bowen, Archives of Neurology	2002	786

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