J. Haines

发表

ApoE-4 and Age at Onset of Alzheimer's Disease

J. Haines, M. Albert, D. Blacker, 1997, Neurology.

Genetic variation among 82 pharmacogenes: The PGRNseq data from the eMERGE network

Melissa A. Basford, John J. Connolly, Terrie E. Kitchner, 2016, Clinical pharmacology and therapeutics.

Genetic overlap between Alzheimer’s disease and Parkinson’s disease at the MAPT locus

A Smith, M A Pericak-Vance, L A Farrer, 2015, Molecular Psychiatry.

Genome-wide association study of Alzheimer's disease

M A Pericak-Vance, O L Lopez, E Feingold, 2012, Translational Psychiatry.

Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

D. G. Clark, M. Fornage, A. Hofman, 2018, Alzheimer's & dementia.

Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

J. Gallacher, M. Fornage, I. Giegling, 2018, bioRxiv.

Linkage and Association Study of Late‐Onset Alzheimer Disease Families Linked to 9p21.3

J. Gilbert, M. Pericak-Vance, S. Züchner, 2008, Annals of human genetics.

REPORT on the Fourth International Workshop on Chromosome 9: held at Williamsburg, Virginia, USA, April 23–25, 1995

M. Pericak-Vance, J. Attwood, O. Olopade, 1995 .

Hereditary spastic paraplegia

G. Rouleau, T. Bird, M. Dubé, 2006, Current neurology and neuroscience reports.

Report and abstracts of the Third International Workshop on Chromosome 9. Cambridge, United Kingdom, 9-11 April, 1994.

S. Povey, J. Armour, J. Haines, 1994, Annals of human genetics.

REPORT on the Third International Workshop on Chromosome 9

S. Povey, J. Armour, J. Haines, 1994 .

Report and abstracts of the First International Workshop on Chromosome 9. Held at Girton College Cambridge, UK, 22-24 March, 1992.

S. Povey, D. Kwiatkowski, I. Jackson, 1992, Annals of human genetics.

REPORT on the First International Workshop on Chromosome 9 held at Girton College Cambridge, UK, 22–24 March, 1992

S. Povey, D. Kwiatkowski, I. Jackson, 1992 .

The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility

H. Ullum, H. Hakonarson, M. Pericak-Vance, 2017, bioRxiv.

Molecular Genetics of Familial Alzheimer's Disease

L. Farrer, J. Haines, R. Polinsky, 1989, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

Confirmation of linkage of type 1 hereditary sensory neuropathy to human chromosome 9q22

J. Haines, D. McKenna-Yasek, B. Hosler, 1999, Neurology.

REPORT on the Fifth International Workshop on Chromosome 9 held at Eynsham, Oxfordshire, UK, September 4–6, 1996

M. Pericak-Vance, J. Attwood, O. Olopade, 1997, Annals of human genetics.

Novel mutations detected in the TSC2 gene from both sporadic and familial TSC patients.

M. Short, S. Jóźwiak, V. Ramesh, 1996, Human molecular genetics.

Follow-up of loci from the International Genomics of Alzheimer's Disease Project identifies TRIP4 as a novel susceptibility gene

M. Nöthen, M. Pericak-Vance, F. Jessen, 2014, Translational Psychiatry.

Genetically meaningful phenotypic subgroups in autism spectrum disorders

M. Pericak-Vance, J. Veenstra-VanderWeele, J. Haines, 2014, Genes, brain, and behavior.

Variations in COL15A1 and COL18A1 influence age of onset of primary open angle glaucoma

Catherine E. Braine, J. Haines, L. Pasquale, 2013, Clinical genetics.

Identification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1

J. Haines, D. Kwiatkowski, E. Henske, 1994, Annals of human genetics.

Polymorphisms of the Tumor Suppressor Gene LSAMP are Associated with Left Main Coronary Artery Disease

M. Pericak-Vance, C. Granger, S. Gregory, 2008, Annals of human genetics.

Exome Sequencing of Extended Families with Alzheimer’s Disease Identifies Novel Genes Implicated in Cell Immunity and Neuronal Function

M. Pericak-Vance, J. Jaworski, J. Haines, 2017, Journal of Alzheimer's disease & Parkinsonism.

Serum Lipids in the GENECARD Study of Coronary Artery Disease Identify Quantitative Trait Loci and Phenotypic Subsets on Chromosomes 3q and 5q

J. Haines, W. Kraus, C. Granger, 2006, Annals of human genetics.

Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)

M. Pericak-Vance, G. Schellenberg, R. Mayeux, 2013, Translational Psychiatry.

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid‐compulsive subset of autism

J. Sutcliffe, S. Folstein, R. Blakely, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Evidence for major gene inheritance of Alzheimer disease in families of patients with and without apolipoprotein E epsilon 4.

J. Haines, J. Growdon, C. Duijn, 1996, American journal of human genetics.

Examination of tetrahydrobiopterin pathway genes in autism

J. Gilbert, M. Pericak-Vance, N. Schnetz-Boutaud, 2009, Genes, brain, and behavior.

Examination of association to autism of common genetic variationin genes related to dopamine

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2008, Autism research : official journal of the International Society for Autism Research.

Award Number: W81XWH-12-1-0013 TITLE: Whole Exome Analysis of Early Onset Alzheimer’s Disease PRINCIPAL INVESTIGATOR: Margaret Pericak-Vance CONTRACTING ORGANIZATION: University of Miami

J. Gilbert, E. Martin, J. Vance, 2016 .

Lack of association between UBQLN1 and Alzheimer disease

J. Gilbert, M. Pericak-Vance, P. Doraiswamy, 2006, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.

Preferential preservation of visuospatial memory over verbal memory in the Old Order Amish

Yeunjoo E. Song, M. Pericak-Vance, W. Scott, 2021, medRxiv.

A Genome‐wide Scan in an Amish Pedigree with Parkinsonism

J. Haines, N. Schnetz-Boutaud, D. Murdock, 2008, Annals of human genetics.

The National Institute on Aging Late Onset Alzheimer's Disease Family Based Study: A Critical Component of the International Effort to Understand Alzheimer's Disease

M. Pericak-Vance, D. Bennett, R. Mayeux, 2021, medRxiv.

Exome sequencing identifies novel AD-associated genes.

Nick C Fox, R. Redon, D. Grozeva, 2020, medRxiv.

Chromosome 17q22–q24 and multiple sclerosis genetic susceptibility

M. Pericak-Vance, M. Clanet, F. Clerget-Darpoux, 1999, Genes and Immunity.

Interaction between the α-T catenin gene (VR22) and APOE in Alzheimer’s disease

J. Gilbert, M. Pericak-Vance, D. Schmechel, 2005, Journal of Medical Genetics.

Linkage investigation of three putative tuberous sclerosis determining loci on chromosomes 9q, llq, and 12q

M. Pericak-Vance, Cardiff, S. Povey, 2022 .

Dense linkage disequilibrium mapping in the 15q11–q13 maternal expression domain yields evidence for association in autism

J. Sutcliffe, S. Folstein, J. Haines, 2003, Molecular Psychiatry.

Complete Genomic Screen in Late-Onset Familial Alzheimer’s Disease

J. Haines, M. Pericak-Vance, G. Small, 1998, Neurobiology of Aging.