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You searched for: Author/Creator Schellenberg, Gerard

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1. A platform for discovery: The University of Pennsylvania Integrated Neurodegenerative Disease Biobank. Issue 4 (26th August 2013)

2. A rare missense variant of CASP7 is associated with familial late‐onset Alzheimer's disease. Issue 3 (29th November 2018)

3. Impact of apolipoprotein E genotypes on vitamin E and memantine treatment outcomes in Alzheimer's disease. Issue 1 (25th July 2018)

4. Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease. Issue 1 (31st December 2021)

5. Neuropathological lesions and their contribution to dementia and cognitive impairment in a heterogeneous clinical population. Issue 12 (9th February 2022)

6. O3‐03‐04: A HIGH RESOLUTION CAPTURE‐C PROMOTER INTERACTOME IMPLICATES CAUSAL GENES AT ALZHEIMER'S DISEASE GWAS LOCI. (1st July 2006)

7. O3–01–02: Exome array analysis identifies novel risk variants for non‐familial early‐onset Alzheimer's disease. (1st July 2013)

8. O3–01–04: The identification of rare variants in late‐onset Alzheimer's disease using extended families. (1st July 2013)

9. O4–06–04: Late‐onset Alzheimer's disease neuropathology genomic screen identifies novel loci for neuritic plaque and other Alzheimer's neuropathology features. (1st July 2013)

10. O4–06–05: SORL1 is genetically associated with late‐onset Alzheimer's disease in Japanese, Koreans and Caucasians. (1st July 2013)