User profiles for Melvin McInnis
Melvin G McinnisProfessor of Psychiatry, University of Michigan Verified email at umich.edu Cited by 34961 |
Genome-wide association study identifies 30 loci associated with bipolar disorder
Bipolar disorder is a highly heritable psychiatric disorder. We performed a genome-wide
association study (GWAS) including 20,352 cases and 31,358 controls of European descent, …
association study (GWAS) including 20,352 cases and 31,358 controls of European descent, …
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene
…, W Van Hul, F van Harskamp, A Warren, MG McInnis… - Nature …, 1992 - nature.com
Several families with an early–onset form of familial Alzheimer's disease have been found to
harbour mutations at a specific codon (717) of the gene for the β–amyloid precursor protein (…
harbour mutations at a specific codon (717) of the gene for the β–amyloid precursor protein (…
Alpha-2 macroglobulin is genetically associated with Alzheimer disease
…, RCP Go, R Perry, B Watson, SS Bassett, MG McInnis… - Nature …, 1998 - nature.com
Alpha-2-macroglobulin (α-2 M; encoded by the gene A2M) is a serum pan-protease inhibitor
that has been implicated in Alzheimer disease (AD) based on its ability to mediate the …
that has been implicated in Alzheimer disease (AD) based on its ability to mediate the …
Harmonization of cortical thickness measurements across scanners and sites
With the proliferation of multi-site neuroimaging studies, there is a greater need for handling
non-biological variance introduced by differences in MRI scanners and acquisition protocols…
non-biological variance introduced by differences in MRI scanners and acquisition protocols…
Evidence for genetic linkage of Alzheimer's disease to chromosome 10q
…, D Keeney, J Jones, S Basu, S Yhu, MG McInnis… - Science, 2000 - science.org
Recent studies suggest that insulin-degrading enzyme (IDE) in neurons and microglia degrades
Aβ, the principal component of β-amyloid and one of the neuropathological hallmarks of …
Aβ, the principal component of β-amyloid and one of the neuropathological hallmarks of …
Psychiatric genetics: progress amid controversy
Several psychiatric disorders — such as bipolar disorder, schizophrenia and autism — are
highly heritable, yet identifying their genetic basis has been challenging, with most …
highly heritable, yet identifying their genetic basis has been challenging, with most …
Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12
SE Holmes, EE O'Hearn, MG McInnis… - Nature …, 1999 - nature.com
The genetic aetiologies of at least 20% of autosomal dominant spinocerebellar ataxias (SCAs)
have yet to be elucidated 1. We have recently identified a novel form of autosomal …
have yet to be elucidated 1. We have recently identified a novel form of autosomal …
[PDF][PDF] Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder
…, T Reich, JP Rice, A Goate, MG McInnis… - The American Journal of …, 2003 - cell.com
Genome scans of bipolar disorder (BPD) have not produced consistent evidence for linkage.
The rank-based genome scan meta-analysis (GSMA) method was applied to 18 BPD …
The rank-based genome scan meta-analysis (GSMA) method was applied to 18 BPD …
Genome-wide association study of bipolar disorder in European American and African American individuals
To identify bipolar disorder (BD) genetic susceptibility factors, we conducted two genome-wide
association (GWA) studies: one involving a sample of individuals of European ancestry (…
association (GWA) studies: one involving a sample of individuals of European ancestry (…
Results of a high-resolution genome screen of 437 Alzheimer's disease families
…, GA Chase, MF Folstein, MG McInnis… - Human molecular …, 2003 - academic.oup.com
Alzheimer's disease (AD) is a devastating neurodegenerative disorder of late life with
complex inheritance. Mutations in three known genes lead to the rare early-onset autosomal …
complex inheritance. Mutations in three known genes lead to the rare early-onset autosomal …