Gerard Schellenberg

1.6k citations

23 papers · 811 indexed · h-index 11

Impact in

Clinical Biochemistry top 1%
- Paraoxonase enzyme and polymorphisms
Oral Surgery top 5%
- Oral and Maxillofacial Pathology

Papers in ⓘ

Genetics 9
- Genetic Associations and Epidemiology 5
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 2
Clinical Biochemistry 4
- Paraoxonase enzyme and polymorphisms 3

Co-authors: Rebecca J. Richter (3 shared papers)Laura S. Rozek (3 shared papers)Clement E. Furlong (3 shared papers)Gail P. Jarvik (3 shared papers)Victoria H. Brophy (2 shared papers)Thomas S. Hatsukami (2 shared papers)Ellen M. Wijsman (5 shared papers)Annette Estes (3 shared papers)
Journals: Alzheimer s & Dementia (8 papers)Current Opinion in Neurology (1 paper)Alzheimer s Research & Therapy (1 paper)Neurology (1 paper)Human Genetics (1 paper)
Partner nations: United States Germany Vietnam

In The Last Decade

Gerard Schellenberg

21 papers receiving 794 citations

Peers

Countries citing papers authored by Gerard Schellenberg

Since Specialization

Citations

This map shows the geographic impact of Gerard Schellenberg's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Gerard Schellenberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Gerard Schellenberg more than expected).

Fields of papers citing papers by Gerard Schellenberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gerard Schellenberg. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Gerard Schellenberg. The network helps show where Gerard Schellenberg may publish in the future.

Co-authors

The 25 scholars most cited alongside Gerard Schellenberg, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Gerard Schellenberg Line = papers co-authored together Gerard Schellenberg links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Paraoxonase (PON1) Phenotype Is a Better Predictor of Vascular Disease Than Is PON1 ₁₉₂ or PON1 ₅₅ Genotype Arteriosclerosis Thrombosis and Vascular Biology ·Gail P. Jarvik, Laura S. Rozek, Victoria H. Brophy, Thomas S. Hatsukami, Rebecca J. Richter, Gerard Schellenberg, Clement E. Furlong	2000	259
2	Genetic heterogeneity in families with hereditary multiple exostoses. PubMed ·April Cook, Wendy H. Raskind, Susan H. Blanton, Richard M. Pauli, Ronald G. Gregg, Claire A. Francomano, Erik G. Puffenberger, Ernest U. Conrad, Gregory A. Schmale, Gerard Schellenberg	1993	166
3	Genetic Investigation of Quantitative Traits Related to Autism: Use of Multivariate Polygenic Models with Ascertainment Adjustment The American Journal of Human Genetics ·Yun Ju Sung, Géraldine Dawson, Jeffrey Munson, Annette Estes, Gerard Schellenberg, Ellen M. Wijsman	2004	87
4	Linkage analysis of familial Alzheimer disease, using chromosome 21 markers. PubMed ·Gerard Schellenberg, M. A. Pericak‐Vance, Ellen M. Wijsman, Deborah K. Moore, P. C. Gaskell, L. A. Yamaoka, Jacqueline Bebout, L. Anderson, K. A. Welsh, Chris M. Clark	1991	56
5	Analysis of paraoxonase (PON1) L55M status requires both genotype and phenotype Pharmacogenetics ·Victoria H. Brophy, Gail P. Jarvik, Rebecca J. Richter, Laura S. Rozek, Gerard Schellenberg, Clement E. Furlong	2000	50
6	The correlation of paraoxonase (PON1) activity with lipid and lipoprotein levels differs with vascular disease status Journal of Lipid Research ·Laura S. Rozek, Thomas S. Hatsukami, Rebecca J. Richter, Jane Ranchalis, Karen Nakayama, Laura McKinstry, David A. Gortner, Edward J. Boyko, Gerard Schellenberg, Clement E. Furlong, Gail P. Jarvik	2005	46
7	Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16 Human Genetics ·Nicola H. Chapman, Annette Estes, Jeff Munson, Raphael Bernier, Sara Jane Webb, Joseph H. Rothstein, Nancy J. Minshew, Géraldine Dawson, Gerard Schellenberg, Ellen M. Wijsman	2010	39
8	A rare missense variant of CASP7 is associated with familial late‐onset Alzheimer's disease Alzheimer s & Dementia ·Xiaoling Zhang, Congcong Zhu, Gary W. Beecham, Badri N. Vardarajan, Yiyi Ma, Daniel Lancour, John J. Farrell, Jaeyoon Chung, (unknown), Richard Mayeux, Jonathan L. Haines, Gerard Schellenberg, Margaret Pericak‐Vance, Kathryn L. Lunetta, Lindsay A. Farrer	2018	30
9	P1‐250: Genome‐Wide Association Study of Late‐Onset Alzheimer Disease Identifies Disease‐Associated Variants in MS4A4/MS4A6E, CD2AP, CD33, and EPHA1 Alzheimer s & Dementia ·Adam C. Naj, Gyungah Jun, Jacqueline Buros, Paul J. Gallins, Lindsay A. Farrer, Jonathan L. Haines, Margaret A. Pericak‐Vance, Gerard Schellenberg	2011	27
10	Progress in Alzheimerʼs disease genetics Current Opinion in Neurology ·Gerard Schellenberg	1995	20
11	Measuring informed consent capacity in an Alzheimer's disease clinical trial Alzheimer s & Dementia Translational Research & Clinical Interventions ·Peter Guarino, Julia E. Vertrees, Sanjay Asthana, Mary Sano, Maria D. Llorente, Muralidhar Pallaki, Susan Love, Gerard Schellenberg, Maurice W. Dysken	2016	10
12	Blood-derived mitochondrial DNA copy number is associated with Alzheimer disease, Alzheimer-related biomarkers and serum metabolites Alzheimer s Research & Therapy ·Tong Tong, Congcong Zhu, John J. Farrell, Zainab Khurshid, (unknown), Eden R. Martin, Margaret A. Pericak‐Vance, Li-San Wang, William S. Bush, Gerard Schellenberg, J. L. Haines, Wei Qiao Qiu, Kathryn L. Lunetta, Lindsay A. Farrer, Xiaoling Zhang	2024	9
13	Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample American Journal of Medical Genetics ·Debby W. Tsuang, Andrew D. Skol, Stephen V. Faraone, Stephen F. Bingham, Keith A. Young, Sarita Prabhudesai, Susan L. Haverstock, Felicitas Mena, A. Shrikumar Menon, Darren Bisset, John Pepple, Fred Sauter, Charlene Baldwin, David J. Weiss, Joseph F. Collins, Michael Boehnke, Gerard Schellenberg, Ming T. Tsuang	2001	2
14	Evidence for genetic linkage of autism to chromosomes 7 and 4 Molecular Psychiatry ·Gerard Schellenberg, Géraldine Dawson, Yun Ju Sung, Annette Estes, Jeff Munson, Elisabeth A. Rosenthal, Joseph H. Rothstein, Pamela Flodman, M. Smith, Hilary Coon, L. Leong, C E Yu, Chris Stodgell, Patricia M. Rodier, M. Anne Spence, Nancy J. Minshew, William M. McMahon, Ellen M. Wijsman	2006	2
15	O3–01–04: The identification of rare variants in late‐onset Alzheimer's disease using extended families Alzheimer s & Dementia ·Martin Kohli, Brian W. Kunkle, Adam C. Naj, Regina M. Carney, Kara L. Hamilton‐Nelson, Sophie Rolati, Patrice L. Whitehead, John R. Gilbert, Eden R. Martin, Gary W. Beecham, Weixin Wang, Richard Mayeux, Jonathan L. Haines, Lindsay A. Farrer, Gerard Schellenberg, Stephan Züchner, Margaret A. Pericak‐Vance	2013	1
16	Whole-Exome Sequencing Of Hispanic Early-Onset Alzheimer Disease Families Identifies Rare Variants In Multiple Alzheimer-Related Genes (S28.003) Neurology ·Christiane Reitz, Brian W. Kunkle, Badri N. Vardarajan, Martin Kohli, Adam C. Naj, Patrice Whitehead, William Perry, Eden R. Martin, Gary W. Beecham, John R. Gilbert, Lindsay A. Farrer, Jonathan L. Haines, Gerard Schellenberg, Margaret A. Pericak‐Vance, Richard Mayeux	2014	1
17	O3–01–02: Exome array analysis identifies novel risk variants for non‐familial early‐onset Alzheimer's disease Alzheimer s & Dementia ·Adam C. Naj, Carlos Cruchaga, Brian W. Kunkle, Shubhabrata Mukherjee, Robert Graham, Timothy W. Behrens, Richard Mayeux, Jonathan L. Haines, Lindsay A. Farrer, Margaret A. Pericak‐Vance, Gerard Schellenberg, Weixin Wang	2013	1
18	P3‐016: ER stress in Alzheimer's disease and PSP: Common disease mechanism? Alzheimer s & Dementia ·Lauren Stutzbach, Michele Hawk, Sid Gilman, Virginia Lee, John Q. Trojanowski, Gerard Schellenberg	2012	1
19	O5‐04‐02: RARE CODING MUTATIONS ASSOCIATED WITH ALZHEIMER DISEASE AND OTHER DEMENTIAS Alzheimer s & Dementia ·Devanshi Patel, Jaeyoon Chung, Jesse Mez, Xiaoling Zhang, Jonathan L. Haines, Margaret A. Pericak‐Vance, Gerard Schellenberg, Kathryn L. Lunetta, Lindsay A. Farrer	2018	1
20	Lewy body pathology in familial (presenilin-2) Alzheimer's disease Neurobiology of Aging ·Mark A. Fishel, Debby W. Tsuang, Murray A. Raskind, David Nochlin, Gerard Schellenberg, Thomas D. Bird, James B. Leverenz	2000	1

About Gerard Schellenberg

Gerard Schellenberg is a scholar working on Genetics, Clinical Biochemistry, Molecular Biology, Cognitive Neuroscience and Physiology, having authored 23 papers that have together received 811 indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Paraoxonase enzyme and polymorphisms (3 papers), Alzheimer's disease research and treatments (3 papers), Autism Spectrum Disorder Research (3 papers), Cynara cardunculus studies (3 papers), Apelin-related biomedical research (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Clinical Biochemistry (323 citations), Oral Surgery (83 citations), Rheumatology (141 citations), Biochemistry (60 citations) and Pharmacology (130 citations). Gerard Schellenberg has collaborated with scholars based in United States, Germany and Vietnam. Frequent co-authors include Rebecca J. Richter, Laura S. Rozek, Clement E. Furlong, Gail P. Jarvik, Victoria H. Brophy, Thomas S. Hatsukami, Ellen M. Wijsman, Annette Estes, Géraldine Dawson and Susan H. Blanton. Their work appears in journals such as Alzheimer s & Dementia, Current Opinion in Neurology, Alzheimer s Research & Therapy, Neurology and Human Genetics.

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