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Gerard Schellenberg

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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TOP 3
Sieh Weiva; Choi Yoonha; Chapman Nicola H; Craig Ulla-Katrina; Steinbart Ellen J; Rothstein Joseph H; Oyanagi Kiyomitsu; Garruto Ralph M; Bird Thomas D; Galasko Douglas R; Schellenberg Gerard D; Wijsman Ellen M
Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates.
Zabetian Cyrus P; Yamamoto Mitsutoshi; Lopez Alexis N; Ujike Hiroshi; Mata Ignacio F; Izumi Yuishin; Kaji Ryuji; Maruyama Hirofumi; Morino Hiroyuki; Oda Masaya; Hutter Carolyn M; Edwards Karen L; Schellenberg Gerard D; Tsuang Debby W; Yearout Dora; Larson Eric B; Kawakami Hideshi
LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.
Guthrie Chris R; Schellenberg Gerard D; Kraemer Brian C
SUT-2 potentiates tau-induced neurotoxicity in Caenorhabditis elegans.

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All Publications

2009: Sieh Weiva; Choi Yoonha; Chapman Nicola H; Craig Ulla-Katrina; Steinbart Ellen J; Rothstein Joseph H; Oyanagi Kiyomitsu; Garruto Ralph M; Bird Thomas D; Galasko Douglas R; Schellenberg Gerard D; Wijsman Ellen M
Identification of novel susceptibility loci for Guam neurodegenerative disease: challenges of genome scans in genetic isolates.
Human molecular genetics 2009;18(19):3725-38.
2009: Zabetian Cyrus P; Yamamoto Mitsutoshi; Lopez Alexis N; Ujike Hiroshi; Mata Ignacio F; Izumi Yuishin; Kaji Ryuji; Maruyama Hirofumi; Morino Hiroyuki; Oda Masaya; Hutter Carolyn M; Edwards Karen L; Schellenberg Gerard D; Tsuang Debby W; Yearout Dora; Larson Eric B; Kawakami Hideshi
LRRK2 mutations and risk variants in Japanese patients with Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2009;24(7):1034-41.
2009: Guthrie Chris R; Schellenberg Gerard D; Kraemer Brian C
SUT-2 potentiates tau-induced neurotoxicity in Caenorhabditis elegans.
Human molecular genetics 2009;18(10):1825-38.
2008: McMillan Pamela; Korvatska Elena; Poorkaj Parvoneh; Evstafjeva Zana; Robinson Linda; Greenup Lynne; Leverenz James; Schellenberg Gerard D; D'Souza Ian
Tau isoform regulation is region- and cell-specific in mouse brain.
The Journal of comparative neurology 2008;511(6):788-803.
2008: Vuletic Simona; Li Ge; Peskind Elaine R; Kennedy Hal; Marcovina Santica M; Leverenz James B; Petrie Eric C; Lee Virginia M-Y; Galasko Douglas; Schellenberg Gerard D; Albers John J
Apolipoprotein E highly correlates with AbetaPP- and tau-related markers in human cerebrospinal fluid.
Journal of Alzheimer's disease : JAD 2008;15(3):409-17.
2008: Borghesani Paul R; Johnson L Clark; Shelton Amy L; Peskind Elaine R; Aylward Elizabeth H; Schellenberg Gerard D; Cherrier Monique M
Altered medial temporal lobe responses during visuospatial encoding in healthy APOE*4 carriers.
Neurobiology of aging 2008;29(7):981-91.
2008: Winton Matthew J; Van Deerlin Vivianna M; Kwong Linda K; Yuan Wuxing; Wood Elisabeth McCarty; Yu Chang-En; Schellenberg Gerard D; Rademakers Rosa; Caselli Richard; Karydas Anna; Trojanowski John Q; Miller Bruce L; Lee Virginia M-Y
A90V TDP-43 variant results in the aberrant localization of TDP-43 in vitro.
FEBS letters 2008;582(15):2252-6.
2008: Van Deerlin Vivianna M; Leverenz James B; Bekris Lynn M; Bird Thomas D; Yuan Wuxing; Elman Lauren B; Clay Dana; Wood Elisabeth McCarty; Chen-Plotkin Alice S; Martinez-Lage Maria; Steinbart Ellen; McCluskey Leo; Grossman Murray; Neumann Manuela; Wu I-Lin; Yang Wei-Shiung; Kalb Robert; Galasko Douglas R; Montine Thomas J; Trojanowski John Q; Lee Virginia M-Y; Schellenberg Gerard D; Yu Chang-En
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.
Lancet neurology 2008;7(5):409-16.
2008: Schultz M R; Lyons M J; Franz C E; Grant M D; Boake C; Jacobson K C; Xian H; Schellenberg G D; Eisen S A; Kremen W S
Apolipoprotein E genotype and memory in the sixth decade of life.
Neurology 2008;70(19 Pt 2):1771-7.
2008: Reger Mark A; Watson G Stennis; Green Pattie S; Baker Laura D; Cholerton Brenna; Fishel Mark A; Plymate Stephen R; Cherrier Monique M; Schellenberg Gerard D; Frey William H; Craft Suzanne
Intranasal insulin administration dose-dependently modulates verbal memory and plasma amyloid-beta in memory-impaired older adults.
Journal of Alzheimer's disease : JAD 2008;13(3):323-31.
2008: Bekris Lynn M; Millard Steven P; Galloway Nichole M; Vuletic Simona; Albers John J; Li Ge; Galasko Douglas R; DeCarli Charles; Farlow Martin R; Clark Chris M; Quinn Joseph F; Kaye Jeffrey A; Schellenberg Gerard D; Tsuang Debby; Peskind Elaine R; Yu Chang-En
Multiple SNPs within and surrounding the apolipoprotein E gene influence cerebrospinal fluid apolipoprotein E protein levels.
Journal of Alzheimer's disease : JAD 2008;13(3):255-66.
2008: Basun Hans; Bogdanovic Nenad; Ingelsson Martin; Almkvist Ove; Näslund Jan; Axelman Karin; Bird Thomas D; Nochlin David; Schellenberg Gerard D; Wahlund Lars-Olof; Lannfelt Lars
Clinical and neuropathological features of the arctic APP gene mutation causing early-onset Alzheimer disease.
Archives of neurology 2008;65(4):499-505.
2008: Mata Ignacio F; Samii Ali; Schneer Seth H; Roberts John W; Griffith Alida; Leis Berta C; Schellenberg Gerard D; Sidransky Ellen; Bird Thomas D; Leverenz James B; Tsuang Debby; Zabetian Cyrus P
Glucocerebrosidase gene mutations: a risk factor for Lewy body disorders.
Archives of neurology 2008;65(3):379-82.
2008: Jayadev Suman; Steinbart Ellen J; Chi Yueh-Yun; Kukull Walter A; Schellenberg Gerard D; Bird Thomas D
Conjugal Alzheimer disease: risk in children when both parents have Alzheimer disease.
Archives of neurology 2008;65(3):373-8.
2008: Crawford Dana C; Nord Alex S; Badzioch Michael D; Ranchalis Jane; McKinstry Laura A; Ahearn Magdalena; Bertucci Caterina; Shephard Cynthia; Wong Michelle; Rieder Mark J; Schellenberg Gerard D; Nickerson Deborah A; Heagerty Patrick J; Wijsman Ellen M; Jarvik Gail P
A common VLDLR polymorphism interacts with APOE genotype in the prediction of carotid artery disease risk.
Journal of lipid research 2008;49(3):588-96.
2008: Brune Camille W; Korvatska Elena; Allen-Brady Kristina; Cook Edwin H; Dawson Geraldine; Devlin Bernie; Estes Annette; Hennelly Meghann; Hyman Susan L; McMahon William M; Munson Jeffrey; Rodier Patricia M; Schellenberg Gerard D; Stodgell Christopher J; Coon Hilary
Heterogeneous association between engrailed-2 and autism in the CPEA network.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008;147B(2):187-93.
2007: Sonnen Joshua A; Larson Eric B; Crane Paul K; Haneuse Sebastien; Li Ge; Schellenberg Gerald D; Craft Suzanne; Leverenz James B; Montine Thomas J
Pathological correlates of dementia in a longitudinal, population-based sample of aging.
Annals of neurology 2007;62(4):406-13.
2007: Rademakers Rosa; Baker Matt; Gass Jennifer; Adamson Jennifer; Huey Edward D; Momeni Parastoo; Spina Salvatore; Coppola Giovanni; Karydas Anna M; Stewart Heather; Johnson Nancy; Hsiung Ging-Yuek; Kelley Brendan; Kuntz Karen; Steinbart Ellen; Wood Elisabeth McCarty; Yu Chang-En; Josephs Keith; Sorenson Eric; Womack Kyle B; Weintraub Sandra; Pickering-Brown Stuart M; Schofield Peter R; Brooks William S; Van Deerlin Vivianna M; Snowden Julie; Clark Christopher M; Kertesz Andrew; Boylan Kevin; Ghetti Bernardino; Neary David; Schellenberg Gerard D; Beach Thomas G; Mesulam Marsel; Mann David; Grafman Jordan; Mackenzie Ian R; Feldman Howard; Bird Thomas; Petersen Ron; Knopman David; Boeve Bradley; Geschwind Dan H; Miller Bruce; Wszolek Zbigniew; Lippa Carol; Bigio Eileen H; Dickson Dennis; Graff-Radford Neill; Hutton Mike
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.
Lancet neurology 2007;6(10):857-68.
2007: Brickell Kiri L; Leverenz James B; Steinbart Ellen J; Rumbaugh Malia; Schellenberg Gerard D; Nochlin David; Lampe Thomas H; Holm Ida E; Van Deerlin Vivianna; Yuan Wuxing; Bird Thomas D
Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease.
Journal of neurology, neurosurgery, and psychiatry 2007;78(10):1050-5.
2007: Li G; Sokal I; Quinn J F; Leverenz J B; Brodey M; Schellenberg G D; Kaye J A; Raskind M A; Zhang J; Peskind E R; Montine T J
CSF tau/Abeta42 ratio for increased risk of mild cognitive impairment: a follow-up study.
Neurology 2007;69(7):631-9.
2007: Kraemer Brian C; Schellenberg Gerard D
SUT-1 enables tau-induced neurotoxicity in C. elegans.
Human molecular genetics 2007;16(16):1959-71.
2007: Wassink Thomas H; Hazlett Heather C; Epping Eric A; Arndt Stephan; Dager Stephen R; Schellenberg Gerard D; Dawson Geraldine; Piven Joseph
Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism.
Archives of general psychiatry 2007;64(6):709-17.
2007: Yu Chang-En; Seltman Howard; Peskind Elaine R; Galloway Nichole; Zhou Peter X; Rosenthal Elisabeth; Wijsman Ellen M; Tsuang Debby W; Devlin Bernie; Schellenberg Gerard D
Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.
Genomics 2007;89(6):655-65.
2007: Galasko D; Salmon D; Gamst A; Olichney J; Thal L J; Silbert L; Kaye J; Brooks P; Adonay R; Craig U-K; Schellenberg G; Borenstein A R
Prevalence of dementia in Chamorros on Guam: relationship to age, gender, education, and APOE.
Neurology 2007;68(21):1772-81.
2007: Borenstein A R; Mortimer J A; Schofield E; Wu Y; Salmon D P; Gamst A; Olichney J; Thal L J; Silbert L; Kaye J; Craig U L; Schellenberg G D; Galasko D R
Cycad exposure and risk of dementia, MCI, and PDC in the Chamorro population of Guam.
Neurology 2007;68(21):1764-71.
2007: Leverenz J B; Yu C E; Montine T J; Steinbart E; Bekris L M; Zabetian C; Kwong L K; Lee V M-Y; Schellenberg G D; Bird T D
A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.
Brain : a journal of neurology 2007;130(Pt 5):1360-74.
2007: Dawson Geraldine; Estes Annette; Munson Jeffrey; Schellenberg Gerard; Bernier Raphael; Abbott Robert
Quantitative assessment of autism symptom-related traits in probands and parents: Broader Phenotype Autism Symptom Scale.
Journal of autism and developmental disorders 2007;37(3):523-36.
2007: Sundar Purnima Desai; Yu Chang-En; Sieh Weiva; Steinbart Ellen; Garruto Ralph M; Oyanagi Kiyomitsu; Craig Ulla-Katrina; Bird Thomas D; Wijsman Ellen M; Galasko Douglas R; Schellenberg Gerard D
Two sites in the MAPT region confer genetic risk for Guam ALS/PDC and dementia.
Human molecular genetics 2007;16(3):295-306.
2007: Kay Denise M; Moran Dawn; Moses Lina; Poorkaj Parvoneh; Zabetian Cyrus P; Nutt John; Factor Stewart A; Yu Chang-En; Montimurro Jennifer S; Keefe Robert G; Schellenberg Gerard D; Payami Haydeh
Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.
Annals of neurology 2007;61(1):47-54.
2007: Sieh Weiva; Yu Chang-En; Bird Thomas D; Schellenberg Gerard D; Wijsman Ellen M
Accounting for linkage disequilibrium among markers in linkage analysis: impact of haplotype frequency estimation and molecular haplotypes for a gene in a candidate region for Alzheimer's disease.
Human heredity 2007;63(1):26-34.
2007: Kraemer Brian; Schellenberg Gerard D
Using Caenorhabditis elegans models of neurodegenerative disease to identify neuroprotective strategies.
International review of neurobiology 2007;77():219-46.
2006: Riekse Robert G; Li Ge; Petrie Eric C; Leverenz James B; Vavrek Darcy; Vuletic Simona; Albers John J; Montine Thomas J; Lee Virginia M-Y; Lee Michael; Seubert Peter; Galasko Douglas; Schellenberg Gerard D; Hazzard William R; Peskind Elaine R
Effect of statins on Alzheimer's disease biomarkers in cerebrospinal fluid.
Journal of Alzheimer's disease : JAD 2006;10(4):399-406.
2006: Schellenberg G D; Dawson G; Sung Y J; Estes A; Munson J; Rosenthal E; Rothstein J; Flodman P; Smith M; Coon H; Leong L; Yu C-E; Stodgell C; Rodier P M; Spence M A; Minshew N; McMahon W M; Wijsman E M
Evidence for multiple loci from a genome scan of autism kindreds.
Molecular psychiatry 2006;11(11):1049-60, 979.
2006: Li Ge; Cherrier Monique M; Tsuang Debby W; Petrie Eric C; Colasurdo Elizabeth A; Craft Suzanne; Schellenberg Gerard D; Peskind Elaine R; Raskind Murray A; Wilkinson Charles W
Salivary cortisol and memory function in human aging.
Neurobiology of aging 2006;27(11):1705-14.
2006: Brickell Kiri L; Steinbart Ellen J; Rumbaugh Malia; Payami Haydeh; Schellenberg Gerard D; Van Deerlin Vivianna; Yuan Wuxing; Bird Thomas D
Early-onset Alzheimer disease in families with late-onset Alzheimer disease: a potential important subtype of familial Alzheimer disease.
Archives of neurology 2006;63(9):1307-11.
2006: Tsuang Debby W; Riekse Robert G; Purganan Kristina M; David Andrew C; Montine Thomas J; Schellenberg Gerard D; Steinbart Ellen J; Petrie Eric C; Bird Thomas D; Leverenz James B
Lewy body pathology in late-onset familial Alzheimer's disease: a clinicopathological case series.
Journal of Alzheimer's disease : JAD 2006;9(3):235-42.
2006: Ramos Erin M; Lin Ming-Tesh; Larson Eric B; Maezawa Izumi; Tseng Li-Hui; Edwards Karen L; Schellenberg Gerard D; Hansen John A; Kukull Walter A; Jin Lee-Way
Tumor necrosis factor alpha and interleukin 10 promoter region polymorphisms and risk of late-onset Alzheimer disease.
Archives of neurology 2006;63(8):1165-9.
2006: Peskind Elaine R; Li Ge; Shofer Jane; Quinn Joseph F; Kaye Jeffrey A; Clark Chris M; Farlow Martin R; DeCarli Charles; Raskind Murray A; Schellenberg Gerard D; Lee Virginia M-Y; Galasko Douglas R
Age and apolipoprotein E*4 allele effects on cerebrospinal fluid beta-amyloid 42 in adults with normal cognition.
Archives of neurology 2006;63(7):936-9.
2006: Kraemer Brian C; Burgess Jack K; Chen Jin H; Thomas James H; Schellenberg Gerard D
Molecular pathways that influence human tau-induced pathology in Caenorhabditis elegans.
Human molecular genetics 2006;15(9):1483-96.
2006: Malkani Roneil; D'Souza Ian; Gwinn-Hardy Katrina; Schellenberg Gerard D; Hardy John; Momeni Parastoo
A MAPT mutation in a regulatory element upstream of exon 10 causes frontotemporal dementia.
Neurobiology of disease 2006;22(2):401-3.
2006: Carlson Christopher S; Heagerty Patrick J; Hatsukami Thomas S; Richter Rebecca J; Ranchalis Jane; Lewis Julieann; Bacus Tamara J; McKinstry Laura A; Schellenberg Gerard D; Rieder Mark; Nickerson Deborah; Furlong Clement E; Chait Alan; Jarvik Gail P
TagSNP analyses of the PON gene cluster: effects on PON1 activity, LDL oxidative susceptibility, and vascular disease.
Journal of lipid research 2006;47(5):1014-24.
2006: Leverenz James B; Fishel Mark A; Peskind Elaine R; Montine Thomas J; Nochlin David; Steinbart Ellen; Raskind Murray A; Schellenberg Gerard D; Bird Thomas D; Tsuang Debby
Lewy body pathology in familial Alzheimer disease: evidence for disease- and mutation-specific pathologic phenotype.
Archives of neurology 2006;63(3):370-6.
2006: Reger M A; Watson G S; Frey W H; Baker L D; Cholerton B; Keeling M L; Belongia D A; Fishel M A; Plymate S R; Schellenberg G D; Cherrier M M; Craft S
Effects of intranasal insulin on cognition in memory-impaired older adults: modulation by APOE genotype.
Neurobiology of aging 2006;27(3):451-8.
2006: D'Souza Ian; Schellenberg Gerard D
Arginine/serine-rich protein interaction domain-dependent modulation of a tau exon 10 splicing enhancer: altered interactions and mechanisms for functionally antagonistic FTDP-17 mutations Delta280K AND N279K.
The Journal of biological chemistry 2006;281(5):2460-9.
2006: Zabetian Cyrus P; Lauricella Chris J; Tsuang Debby W; Leverenz James B; Schellenberg Gerard D; Payami Haydeh
Analysis of the LRRK2 G2019S mutation in Alzheimer Disease.
Archives of neurology 2006;63(1):156-7.
2006: Schellenberg Gerard D
Early Alzheimer's disease genetics.
Journal of Alzheimer's disease : JAD 2006;9(3 Suppl):367-72.
2005: Li Xiaohong; Rowland Lewis P; Mitsumoto Hiroshi; Przedborski Serge; Bird Thomas D; Schellenberg Gerard D; Peskind Elaine; Johnson Nancy; Siddique Teepu; Mesulam M-Marsel; Weintraub Sandra; Mastrianni James A
Prion protein codon 129 genotype prevalence is altered in primary progressive aphasia.
Annals of neurology 2005;58(6):858-64.
2005: Swan Gary E; Lessov-Schlaggar Christina N; Carmelli Dorit; Schellenberg Gerard D; La Rue Asenath
Apolipoprotein E epsilon4 and change in cognitive functioning in community-dwelling older adults.
Journal of geriatric psychiatry and neurology 2005;18(4):196-201.
2005: Devlin B; Cook E H; Coon H; Dawson G; Grigorenko E L; McMahon W; Minshew N; Pauls D; Smith M; Spence M A; Rodier P M; Stodgell C; Schellenberg G D;
Autism and the serotonin transporter: the long and short of it.
Molecular psychiatry 2005;10(12):1110-6.
2005: Rademakers Rosa; Melquist Stacey; Cruts Marc; Theuns Jessie; Del-Favero Jurgen; Poorkaj Parvoneh; Baker Matt; Sleegers Kristel; Crook Richard; De Pooter Tim; Bel Kacem Samira; Adamson Jennifer; Van den Bossche Dirk; Van den Broeck Marleen; Gass Jennifer; Corsmit Ellen; De Rijk Peter; Thomas Natalie; Engelborghs Sebastiaan; Heckman Michael; Litvan Irene; Crook Julia; De Deyn Peter P; Dickson Dennis; Schellenberg Gerard D; Van Broeckhoven Christine; Hutton Michael L
High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
Human molecular genetics 2005;14(21):3281-92.
2005: Faraone S V; Skol A D; Tsuang D W; Young K A; Haverstock S L; Prabhudesai S; Mena F; Menon A S; Leong L; Sautter F; Baldwin C; Bingham S; Weiss D; Collins J; Keith T; Vanden Eng J L; Boehnke M; Tsuang M T; Schellenberg G D
Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;139B(1):91-100.
2005: Li G; Shofer J B; Kukull W A; Peskind E R; Tsuang D W; Breitner J C S; McCormick W; Bowen J D; Teri L; Schellenberg G D; Larson E B
Serum cholesterol and risk of Alzheimer disease: a community-based cohort study.
Neurology 2005;65(7):1045-50.
2005: Rozek Laura S; Hatsukami Thomas S; Richter Rebecca J; Ranchalis Jane; Nakayama Karen; McKinstry Laura A; Gortner David A; Boyko Edward; Schellenberg Gerard D; Furlong Clement E; Jarvik Gail P
The correlation of paraoxonase (PON1) activity with lipid and lipoprotein levels differs with vascular disease status.
Journal of lipid research 2005;46(9):1888-95.
2005: Hall D A; Leehey M A; Filley C M; Steinbart E; Montine T; Schellenberg G D; Bosque P; Nixon R; Bird T
PRNP H187R mutation associated with neuropsychiatric disorders in childhood and dementia.
Neurology 2005;64(7):1304-6.
2005: Hendrickson Audrey; McKinstry Laura A; Lewis Julieann K; Lum Jeremy; Louie Andy; Schellenberg Gerard D; Hatsukami Thomas S; Chait Alan; Jarvik Gail P
Ex vivo measures of LDL oxidative susceptibility predict carotid artery disease.
Atherosclerosis 2005;179(1):147-53.
2005: Borenstein Amy R; Wu Yougui; Mortimer James A; Schellenberg Gerard D; McCormick Wayne C; Bowen James D; McCurry Susan; Larson Eric B
Developmental and vascular risk factors for Alzheimer's disease.
Neurobiology of aging 2005;26(3):325-34.
2005: Poorkaj Parvoneh; Moses Lina; Montimurro Jennifer S; Nutt John G; Schellenberg Gerard D; Payami Haydeh
Parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism.
BMC neurology 2005;5(1):4.
2005: D'Souza Ian; Schellenberg Gerard D
Regulation of tau isoform expression and dementia.
Biochimica et biophysica acta 2005;1739(2-3):104-15.
2005: Sung Yun Ju; Dawson Geraldine; Munson Jeffrey; Estes Annette; Schellenberg Gerard D; Wijsman Ellen M
Genetic investigation of quantitative traits related to autism: use of multivariate polygenic models with ascertainment adjustment.
American journal of human genetics 2005;76(1):68-81.
2005: Wijsman Ellen M; Daw E Warwick; Yu Xuesong; Steinbart Ellen J; Nochlin David; Bird Thomas D; Schellenberg Gerard D
APOE and other loci affect age-at-onset in Alzheimer's disease families with PS2 mutation.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005;132B(1):14-20.
2005: Dawson Geraldine; Webb Sara Jane; Wijsman Ellen; Schellenberg Gerard; Estes Annette; Munson Jeffrey; Faja Susan
Neurocognitive and electrophysiological evidence of altered face processing in parents of children with autism: implications for a model of abnormal development of social brain circuitry in autism.
Development and psychopathology 2005;17(3):679-97.
2004: Li G; Higdon R; Kukull W A; Peskind E; Van Valen Moore K; Tsuang D; van Belle G; McCormick W; Bowen J D; Teri L; Schellenberg G D; Larson E B
Statin therapy and risk of dementia in the elderly: a community-based prospective cohort study.
Neurology 2004;63(9):1624-8.
2004: Yu Chang-En; Devlin Bernie; Galloway Nichole; Loomis Elaine; Schellenberg Gerard D
ADLAPH: A molecular haplotyping method based on allele-discriminating long-range PCR.
Genomics 2004;84(3):600-12.
2004: Wijsman Ellen M; Daw E Warwick; Yu Change-En; Payami Haydeh; Steinbart Ellen J; Nochlin David; Conlon Erin M; Bird Thomas D; Schellenberg Gerard D
Evidence for a novel late-onset Alzheimer disease locus on chromosome 19p13.2.
American journal of human genetics 2004;75(3):398-409.
2004: Poorkaj P; Nutt J G; James D; Gancher S; Bird T D; Steinbart E; Schellenberg G D; Payami Haydeh
parkin mutation analysis in clinic patients with early-onset Parkinson [corrected] disease.
American journal of medical genetics. Part A 2004;129A(1):44-50.
2004: Devlin Bernie; Bennett Pamela; Dawson Geraldine; Figlewicz Denise A; Grigorenko Elena L; McMahon William; Minshew Nancy; Pauls David; Smith Moyra; Spence M Anne; Rodier Patricia M; Stodgell Chris; Schellenberg Gerard D;
Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004;126B(1):46-50.
2003: Schellenberg Gerard D
Alzheimer disease genes: presenilin 2 mutation number 9 and still counting.
Archives of neurology 2003;60(11):1521-2.
2003: Longstreth W T; Schellenberg G D; Fahrenbruch C E; Cobb L A; Copass M K; Siscovick D S
Apolipoprotein E genotypes and outcome from out of hospital cardiac arrest.
Journal of neurology, neurosurgery, and psychiatry 2003;74(10):1441-3.
2003: Furukawa Katsutoshi; Wang Yue; Yao Pamela J; Fu Weiming; Mattson Mark P; Itoyama Yasuto; Onodera Hiroshi; D'Souza Ian; Poorkaj Parvone H; Bird Thomas D; Schellenberg Gerard D
Alteration in calcium channel properties is responsible for the neurotoxic action of a familial frontotemporal dementia tau mutation.
Journal of neurochemistry 2003;87(2):427-36.
2003: Kraemer Brian C; Zhang Bin; Leverenz James B; Thomas James H; Trojanowski John Q; Schellenberg Gerard D
Neurodegeneration and defective neurotransmission in a Caenorhabditis elegans model of tauopathy.
Proceedings of the National Academy of Sciences of the United States of America 2003;100(17):9980-5.
2003: Craft Suzanne; Asthana Sanjay; Cook David G; Baker Laura D; Cherrier Monique; Purganan Kristina; Wait Colby; Petrova Andreana; Latendresse Shawn; Watson G Stennis; Newcomer John W; Schellenberg Gerard D; Krohn Aaron J
Insulin dose-response effects on memory and plasma amyloid precursor protein in Alzheimer's disease: interactions with apolipoprotein E genotype.
Psychoneuroendocrinology 2003;28(6):809-22.
2003: Jarvik Gail P; Hatsukami Thomas S; Carlson Chris; Richter Rebecca J; Jampsa Rachel; Brophy Victoria H; Margolin Sadie; Rieder Mark; Nickerson Deborah; Schellenberg Gerard D; Heagerty Patrick J; Furlong Clement E
Paraoxonase activity, but not haplotype utilizing the linkage disequilibrium structure, predicts vascular disease.
Arteriosclerosis, thrombosis, and vascular biology 2003;23(8):1465-71.
2003: Skol A D; Young K A; Tsuang D W; Faraone S V; Haverstock S L; Bingham S; Prabhudesai S; Mena F; Menon A S; Yu Chang-En; Rundell Paul; Pepple J; Sauter F; Baldwin C; Weiss D; Collins J; Keith T; Boehnke M; Schellenberg G D; Tsuang M T
Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large Veterans Affairs Cooperative Study sample.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003;118B(1):8-15.
2003: Cook David G; Leverenz James B; McMillan Pamela J; Kulstad J Jacob; Ericksen Sasha; Roth Richard A; Schellenberg Gerard D; Jin Lee-Way; Kovacina Kristina S; Craft Suzanne
Reduced hippocampal insulin-degrading enzyme in late-onset Alzheimer's disease is associated with the apolipoprotein E-epsilon4 allele.
The American journal of pathology 2003;162(1):313-9.
2002: Kukull Walter A; Higdon Roger; Bowen James D; McCormick Wayne C; Teri Linda; Schellenberg Gerard D; van Belle Gerald; Jolley Lance; Larson Eric B
Dementia and Alzheimer disease incidence: a prospective cohort study.
Archives of neurology 2002;59(11):1737-46.
2002: Poorkaj Parvoneh; Muma Nancy A; Zhukareva Victoria; Cochran Elizabeth J; Shannon Kathleen M; Hurtig Howard; Koller William C; Bird Thomas D; Trojanowski John Q; Lee Virginia M-Y; Schellenberg Gerard D
An R5L tau mutation in a subject with a progressive supranuclear palsy phenotype.
Annals of neurology 2002;52(4):511-6.
2002: Devlin Bernie; Bennett Pamela; Cook Edwin H; Dawson Geraldine; Gonen David; Grigorenko Elena L; McMahon William; Pauls David; Smith Moyra; Spence M Anne; Schellenberg Gerard D;
No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.
American journal of medical genetics 2002;114(6):667-72.
2002: Faraone Stephen V; Skol Andrew D; Tsuang Debby W; Bingham Stephen; Young Keith A; Prabhudesai Sarita; Haverstock Susan L; Mena Felicitas; Menon Aerath Sri Kumar; Bisset Darren; Pepple John; Sautter Fred; Baldwin Charlene; Weiss David; Collins Joseph; Keith Tim; Boehnke Michael; Tsuang Ming T; Schellenberg G D
Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample.
American journal of medical genetics 2002;114(6):598-604.
2002: Jarvik Gail P; Tsai Nancey Trevanian; McKinstry Laura A; Wani Roohi; Brophy Victoria H; Richter Rebecca J; Schellenberg Gerard D; Heagerty Patrick J; Hatsukami Thomas S; Furlong Clement E
Vitamin C and E intake is associated with increased paraoxonase activity.
Arteriosclerosis, thrombosis, and vascular biology 2002;22(8):1329-33.
2002: Sultana Razia; Yu Chang-En; Yu Jun; Munson Jeffery; Chen Donghui; Hua Wenhui; Estes Annette; Cortes Fanny; de la Barra Flora; Yu Dongmei; Haider Syed T; Trask Barbara J; Green Eric D; Raskind Wendy H; Disteche Christine M; Wijsman Ellen; Dawson Geraldine; Storm Daniel R; Schellenberg Gerard D; Villacres Enrique C
Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins.
Genomics 2002;80(2):129-34.
2002: Yu Chang-En; Dawson Geraldine; Munson Jeffrey; D'Souza Ian; Osterling Julie; Estes Annette; Leutenegger Anne-Louise; Flodman Pamela; Smith Moyra; Raskind Wendy H; Spence M Anne; McMahon William; Wijsman Ellen M; Schellenberg Gerard D
Presence of large deletions in kindreds with autism.
American journal of human genetics 2002;71(1):100-15.
2002: D'Souza Ian; Schellenberg Gerard D
tau Exon 10 expression involves a bipartite intron 10 regulatory sequence and weak 5' and 3' splice sites.
The Journal of biological chemistry 2002;277(29):26587-99.
2002: Zareparsi S; James D M; Kaye J A; Bird T D; Schellenberg G D; Payami H
HLA-A2 homozygosity but not heterozygosity is associated with Alzheimer disease.
Neurology 2002;58(6):973-5.
2002: Edland Steven D; Tobe Vincent O; Rieder Mark J; Bowen James D; McCormick Wayne; Teri Linda; Schellenberg Gerard D; Larson Eric B; Nickerson Deborah A; Kukull Walter A
Mitochondrial genetic variants and Alzheimer disease: a case-control study of the T4336C and G5460A variants.
Alzheimer disease and associated disorders 2002;16(1):1-7.
2002: Galasko D; Salmon D P; Craig U-K; Thal L J; Schellenberg G; Wiederholt W
Clinical features and changing patterns of neurodegenerative disorders on Guam, 1997-2000.
Neurology 2002;58(1):90-7.
2002: Dawson Geraldine; Webb Sara; Schellenberg Gerard D; Dager Stephen; Friedman Seth; Aylward Elizabeth; Richards Todd
Defining the broader phenotype of autism: genetic, brain, and behavioral perspectives.
Development and psychopathology 2002;14(3):581-611.
2001: Tsuang D W; Skol A D; Faraone S V; Bingham S; Young K A; Prabhudesai S; Haverstock S L; Mena F; Menon A S; Bisset D; Pepple J; Sauter F; Baldwin C; Weiss D; Collins J; Boehnke M; Schellenberg G D; Tsuang M T;
Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample.
American journal of medical genetics 2001;105(8):662-8.
2001: Poorkaj P; Tsuang D; Wijsman E; Steinbart E; Garruto R M; Craig U K; Chapman N H; Anderson L; Bird T D; Plato C C; Perl D P; Weiderholt W; Galasko D; Schellenberg G D
TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonism dementia complex of Guam.
Archives of neurology 2001;58(11):1871-8.
2001: Borenstein Graves A; Mortimer J A; Bowen J D; McCormick W C; McCurry S M; Schellenberg G D; Larson E B
Head circumference and incident Alzheimer's disease: modification by apolipoprotein E.
Neurology 2001;57(8):1453-60.
2001: Poorkaj P; Kas A; D'Souza I; Zhou Y; Pham Q; Stone M; Olson M V; Schellenberg G D
A genomic sequence analysis of the mouse and human microtubule-associated protein tau.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(9):700-12.
2001: Moceri V M; Kukull W A; Emanual I; van Belle G; Starr J R; Schellenberg G D; McCormick W C; Bowen J D; Teri L; Larson E B
Using census data and birth certificates to reconstruct the early-life socioeconomic environment and the relation to the development of Alzheimer's disease.
Epidemiology (Cambridge, Mass.) 2001;12(4):383-9.
2001: Peskind E R; Wilkinson C W; Petrie E C; Schellenberg G D; Raskind M A
Increased CSF cortisol in AD is a function of APOE genotype.
Neurology 2001;56(8):1094-8.
2001: Poorkaj P; Grossman M; Steinbart E; Payami H; Sadovnick A; Nochlin D; Tabira T; Trojanowski J Q; Borson S; Galasko D; Reich S; Quinn B; Schellenberg G; Bird T D
Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia.
Archives of neurology 2001;58(3):383-7.
2001: Bird T D; Schellenberg G D
The case of the missing tau, or, why didn't the mRNA bark?
Annals of neurology 2001;49(2):144-5.
2001: Baskin F; Rosenberg R N; Iyer L; Schellenberg G D; Hynan L; Nee L E
Platelet APP isoform ratios in asymptomatic young adults expressing an AD-related presenilin-1 mutation.
Journal of the neurological sciences 2001;183(1):85-8.
2000: Jarvik G P; Rozek L S; Brophy V H; Hatsukami T S; Richter R J; Schellenberg G D; Furlong C E
Paraoxonase (PON1) phenotype is a better predictor of vascular disease than is PON1(192) or PON1(55) genotype.
Arteriosclerosis, thrombosis, and vascular biology 2000;20(11):2441-7.
2000: Poorkaj P; Peterson K R; Schellenberg G D
Single-step conversion of P1 and P1 artificial chromosome clones into yeast artificial chromosomes.
Genomics 2000;68(1):106-10.
2000: Brophy V H; Jarvik G P; Richter R J; Rozek L S; Schellenberg G D; Furlong C E
Analysis of paraoxonase (PON1) L55M status requires both genotype and phenotype.
Pharmacogenetics 2000;10(5):453-60.
2000: D'Souza I; Schellenberg G D
Determinants of 4-repeat tau expression. Coordination between enhancing and inhibitory splicing sequences for exon 10 inclusion.
The Journal of biological chemistry 2000;275(23):17700-9.
2000: Litvan I; Dickson D W; Buttner-Ennever J A; Delacourte A; Hutton M; Dubois B; Golbe L I; Hallett M; Schellenberg G D; Standaert D; Brooks D J; Price D
Research goals in progressive supranuclear palsy. First International Brainstorming Conference on PSP.
Movement disorders : official journal of the Movement Disorder Society 2000;15(3):446-58.
2000: Schellenberg G D; D'Souza I; Poorkaj P
The genetics of Alzheimer's disease.
Current psychiatry reports 2000;2(2):158-64.
2000: Craft S; Asthana S; Schellenberg G; Baker L; Cherrier M; Boyt A A; Martins R N; Raskind M; Peskind E; Plymate S
Insulin effects on glucose metabolism, memory, and plasma amyloid precursor protein in Alzheimer's disease differ according to apolipoprotein-E genotype.
Annals of the New York Academy of Sciences 2000;903():222-8.
2000: Furukawa K; D'Souza I; Crudder C H; Onodera H; Itoyama Y; Poorkaj P; Bird T D; Schellenberg G D
Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism.
Neuroreport 2000;11(1):57-60.
2000: Daw E W; Payami H; Nemens E J; Nochlin D; Bird T D; Schellenberg G D; Wijsman E M
The number of trait loci in late-onset Alzheimer disease.
American journal of human genetics 2000;66(1):196-204.
1999: Tsuang D; Larson E B; Bowen J; McCormick W; Teri L; Nochlin D; Leverenz J B; Peskind E R; Lim A; Raskind M A; Thompson M L; Mirra S S; Gearing M; Schellenberg G D; Kukull W
The utility of apolipoprotein E genotyping in the diagnosis of Alzheimer disease in a community-based case series.
Archives of neurology 1999;56(12):1489-95.
1999: Bretsky P M; Buckwalter J G; Seeman T E; Miller C A; Poirier J; Schellenberg G D; Finch C E; Henderson V W
Evidence for an interaction between apolipoprotein E genotype, gender, and Alzheimer disease.
Alzheimer disease and associated disorders 1999;13(4):216-21.
1999: Graves A B; Bowen J D; Rajaram L; McCormick W C; McCurry S M; Schellenberg G D; Larson E B
Impaired olfaction as a marker for cognitive decline: interaction with apolipoprotein E epsilon4 status.
Neurology 1999;53(7):1480-7.
1999: Yasuda M; Kawamata T; Komure O; Kuno S; D'Souza I; Poorkaj P; Kawai J; Tanimukai S; Yamamoto Y; Hasegawa H; Sasahara M; Hazama F; Schellenberg G D; Tanaka C
A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.
Neurology 1999;53(4):864-8.
1999: Craft S; Asthana S; Schellenberg G; Cherrier M; Baker L D; Newcomer J; Plymate S; Latendresse S; Petrova A; Raskind M; Peskind E; Lofgreen C; Grimwood K
Insulin metabolism in Alzheimer's disease differs according to apolipoprotein E genotype and gender.
Neuroendocrinology 1999;70(2):146-52.
1999: D'Souza I; Poorkaj P; Hong M; Nochlin D; Lee V M; Bird T D; Schellenberg G D
Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements.
Proceedings of the National Academy of Sciences of the United States of America 1999;96(10):5598-603.
1999: Bird T D; Nochlin D; Poorkaj P; Cherrier M; Kaye J; Payami H; Peskind E; Lampe T H; Nemens E; Boyer P J; Schellenberg G D
A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)
Brain : a journal of neurology 1999;122 ( Pt 4)():741-56.
1999: Iijima M; Tabira T; Poorkaj P; Schellenberg G D; Trojanowski J Q; Lee V M; Schmidt M L; Takahashi K; Nabika T; Matsumoto T; Yamashita Y; Yoshioka S; Ishino H
A distinct familial presenile dementia with a novel missense mutation in the tau gene.
Neuroreport 1999;10(3):497-501.
1999: Yasuda M; Maeda K; Hashimoto M; Yamashita H; Ikejiri Y; Bird T D; Tanaka C; Schellenberg G D
A pedigree with a novel presenilin 1 mutation at a residue that is not conserved in presenilin 2.
Archives of neurology 1999;56(1):65-9.
1999: Carmelli D; Swan G E; Reed T; Schellenberg G D; Christian J C
The effect of apolipoprotein E epsilon4 in the relationships of smoking and drinking to cognitive function.
Neuroepidemiology 1999;18(3):125-33.
1998: Hong M; Zhukareva V; Vogelsberg-Ragaglia V; Wszolek Z; Reed L; Miller B I; Geschwind D H; Bird T D; McKeel D; Goate A; Morris J C; Wilhelmsen K C; Schellenberg G D; Trojanowski J Q; Lee V M
Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.
Science (New York, N.Y.) 1998;282(5395):1914-7.
1998: Leverenz J B; Yu C E; Schellenberg G D
Aging-associated neuropathology in Werner syndrome.
Acta neuropathologica 1998;96(4):421-4.
1998: Clark L N; Poorkaj P; Wszolek Z; Geschwind D H; Nasreddine Z S; Miller B; Li D; Payami H; Awert F; Markopoulou K; Andreadis A; D'Souza I; Lee V M; Reed L; Trojanowski J Q; Zhukareva V; Bird T; Schellenberg G; Wilhelmsen K C
Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(22):13103-7.
1998: Hisama F M; Oshima J; Yu C E; Fu Y H; Mulligan J; Weissman S M; Schellenberg G D
Comparison of methods for identifying transcription units and transcription map of the Werner syndrome gene region.
Genomics 1998;52(3):352-7.
1998: Craft S; Teri L; Edland S D; Kukull W A; Schellenberg G; McCormick W C; Bowen J D; Larson E B
Accelerated decline in apolipoprotein E-epsilon4 homozygotes with Alzheimer's disease.
Neurology 1998;51(1):149-53.
1998: Carmelli D; Swan G E; Reed T; Miller B; Wolf P A; Jarvik G P; Schellenberg G D
Midlife cardiovascular risk factors, ApoE, and cognitive decline in elderly male twins.
Neurology 1998;50(6):1580-5.
1998: Furukawa K; Guo Q; Schellenberg G D; Mattson M P
Presenilin-1 mutation alters NGF-induced neurite outgrowth, calcium homeostasis, and transcription factor (AP-1) activation in PC12 cells.
Journal of neuroscience research 1998;52(5):618-24.
1998: Poorkaj P; Bird T D; Wijsman E; Nemens E; Garruto R M; Anderson L; Andreadis A; Wiederholt W C; Raskind M; Schellenberg G D
Tau is a candidate gene for chromosome 17 frontotemporal dementia.
Annals of neurology 1998;43(6):815-25.
1998: Sharma V; Poorkaj P; Hisama F; Bonnycastle L; Yu C E; Massa H; Trask B; Clancy K P; Patterson D; Weissman S M; Schellenberg G D
An expression map from human chromosome 14q24.3.
Genomics 1998;47(2):314-8.
1998: Craft S; Peskind E; Schwartz M W; Schellenberg G D; Raskind M; Porte D
Cerebrospinal fluid and plasma insulin levels in Alzheimer's disease: relationship to severity of dementia and apolipoprotein E genotype.
Neurology 1998;50(1):164-8.
1998: Hubble J P; Kurth J H; Glatt S L; Kurth M C; Schellenberg G D; Hassanein R E; Lieberman A; Koller W C
Gene-toxin interaction as a putative risk factor for Parkinson's disease with dementia.
Neuroepidemiology 1998;17(2):96-104.
1998: Poorkaj P; Sharma V; Anderson L; Nemens E; Alonso M E; Orr H; White J; Heston L; Bird T D; Schellenberg G D
Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene.
Human mutation 1998;11(3):216-21.
1997: Peskind E R; Leverenz J; Farlow M R; Ito R K; Provow S A; Siegel R S; Cleveland M; Morgan C H; Pandian M R; Corbin S; Nochlin D; Schellenberg G D; Raskind M A; Wagner S L
Clinicopathologic correlations of soluble amyloid beta-protein precursor in cerebrospinal fluid in patients with Alzheimer disease and controls.
Alzheimer disease and associated disorders 1997;11(4):201-6.
1997: Zareparsi S; Kaye J; Camicioli R; Grimslid H; Oken B; Litt M; Nutt J; Bird T; Schellenberg G; Payami H
Modulation of the age at onset of Parkinson's disease by apolipoprotein E genotypes.
Annals of neurology 1997;42(4):655-8.
1997: O'Meara E S; Kukull W A; Sheppard L; Bowen J D; McCormick W C; Teri L; Pfanschmidt M; Thompson J D; Schellenberg G D; Larson E B
Head injury and risk of Alzheimer's disease by apolipoprotein E genotype.
American journal of epidemiology 1997;146(5):373-84.
1997: Payami H; Schellenberg G D; Zareparsi S; Kaye J; Sexton G J; Head M A; Matsuyama S S; Jarvik L F; Miller B; McManus D Q; Bird T D; Katzman R; Heston L; Norman D; Small G W
Evidence for association of HLA-A2 allele with onset age of Alzheimer's disease.
Neurology 1997;49(2):512-8.
1997: Jarvik G P; Goode E L; Austin M A; Auwerx J; Deeb S; Schellenberg G D; Reed T
Evidence that the apolipoprotein E-genotype effects on lipid levels can change with age in males: a longitudinal analysis.
American journal of human genetics 1997;61(1):171-81.
1997: Bird T D; Wijsman E M; Nochlin D; Leehey M; Sumi S M; Payami H; Poorkaj P; Nemens E; Rafkind M; Schellenberg G D
Chromosome 17 and hereditary dementia: linkage studies in three non-Alzheimer families and kindreds with late-onset FAD.
Neurology 1997;48(4):949-54.
1997: Yu C E; Oshima J; Wijsman E M; Nakura J; Miki T; Piussan C; Matthews S; Fu Y H; Mulligan J; Martin G M; Schellenberg G D
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.
American journal of human genetics 1997;60(2):330-41.
1997: Tsuang D; Raskind M A; Leverenz J; Peskind E R; Schellenberg G; Bird T D
The effect of apolipoprotein E genotype on expression of an autosomal dominant schizophreniform disorder with progressive dementia and neurofibrillary tangles.
Biological psychiatry 1997;41(2):191-5.
1997: O'Meara E S; Kukull W A; Schellenberg G D; Bowen J D; McCormick W C; Teri L; Pfanschmidt M; Thompson J D; Larson E B
Alzheimer's disease and history of blood transfusion by apolipoprotein-E genotype.
Neuroepidemiology 1997;16(2):86-93.
1996: Bird T D; Levy-Lahad E; Poorkaj P; Sharma V; Nemens E; Lahad A; Lampe T H; Schellenberg G D
Wide range in age of onset for chromosome 1--related familial Alzheimer's disease.
Annals of neurology 1996;40(6):932-6.
1996: Ikeda M; Sharma V; Sumi S M; Rogaeva E A; Poorkaj P; Sherrington R; Nee L; Tsuda T; Oda N; Watanabe M; Aoki M; Shoji M; Abe K; Itoyama Y; Hirai S; Schellenberg G D; Bird T D; St George-Hyslop P H
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patients.
Annals of neurology 1996;40(6):912-7.
1996: Oshima J; Yu C E; Piussan C; Klein G; Jabkowski J; Balci S; Miki T; Nakura J; Ogihara T; Ells J; Smith M; Melaragno M I; Fraccaro M; Scappaticci S; Matthews J; Ouais S; Jarzebowicz A; Schellenberg G D; Martin G M
Homozygous and compound heterozygous mutations at the Werner syndrome locus.
Human molecular genetics 1996;5(12):1909-13.
1996: McMillan P J; Leverenz J B; Poorkaj P; Schellenberg G D; Dorsa D M
Neuronal expression of STM2 mRNA in human brain is reduced in Alzheimer's disease.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 1996;44(11):1215-22.
1996: Rosenberg R N; Richter R W; Risser R C; Taubman K; Prado-Farmer I; Ebalo E; Posey J; Kingfisher D; Dean D; Weiner M F; Svetlik D; Adams P; Honig L S; Cullum C M; Schaefer F V; Schellenberg G D
Genetic factors for the development of Alzheimer disease in the Cherokee Indian.
Archives of neurology 1996;53(10):997-1000.
1996: Kukull W A; Schellenberg G D; Bowen J D; McCormick W C; Yu C E; Teri L; Thompson J D; O'Meara E S; Larson E B
Apolipoprotein E in Alzheimer's disease risk and case detection: a case-control study.
Journal of clinical epidemiology 1996;49(10):1143-8.
1996: Yu C E; Oshima J; Hisama F M; Matthews S; Trask B J; Schellenberg G D
A YAC, P1, and cosmid contig and 17 new polymorphic markers for the Werner syndrome region at 8p12-p21.
Genomics 1996;35(3):431-40.
1996: Nakura J; Miki T; Ye L; Mitsuda N; Zhao Y; Kihara K; Yu C E; Oshima J; Fukuchi K I; Wijsman E M; Schellenberg G D; Martin G M; Murano S i; Hashimoto K; Fujiwara Y; Ogihara T
Narrowing the position of the Werner syndrome locus by homozygosity analysis-extension of homozygosity analysis.
Genomics 1996;36(1):130-41.
1996: Oshima J; Schellenberg G D
[STM-2, a candidate gene for the familial Alzheimer's disease on chromosome 1]
Tanpakushitsu kakusan koso. Protein, nucleic acid, enzyme 1996;41(10):1448-52.
1996: Scheuner D; Eckman C; Jensen M; Song X; Citron M; Suzuki N; Bird T D; Hardy J; Hutton M; Kukull W; Larson E; Levy-Lahad E; Viitanen M; Peskind E; Poorkaj P; Schellenberg G; Tanzi R; Wasco W; Lannfelt L; Selkoe D; Younkin S
Secreted amyloid beta-protein similar to that in the senile plaques of Alzheimer's disease is increased in vivo by the presenilin 1 and 2 and APP mutations linked to familial Alzheimer's disease.
Nature medicine 1996;2(8):864-70.
1996: Levy-Lahad E; Poorkaj P; Wang K; Fu Y H; Oshima J; Mulligan J; Schellenberg G D
Genomic structure and expression of STM2, the chromosome 1 familial Alzheimer disease gene.
Genomics 1996;34(2):198-204.
1996: Goddard K A; Yu C E; Oshima J; Miki T; Nakura J; Piussan C; Martin G M; Schellenberg G D; Wijsman E M
Toward localization of the Werner syndrome gene by linkage disequilibrium and ancestral haplotyping: lessons learned from analysis of 35 chromosome 8p11.1-21.1 markers.
American journal of human genetics 1996;58(6):1286-302.
1996: Tsuang D; Kukull W; Sheppard L; Barnhart R L; Peskind E; Edland S D; Schellenberg G; Raskind M; Larson E B
Impact of sample selection on APOE epsilon 4 allele frequency: a comparison of two Alzheimer's disease samples.
Journal of the American Geriatrics Society 1996;44(6):704-7.
1996: Payami H; Zareparsi S; Montee K R; Sexton G J; Kaye J A; Bird T D; Yu C E; Wijsman E M; Heston L L; Litt M; Schellenberg G D
Gender difference in apolipoprotein E-associated risk for familial Alzheimer disease: a possible clue to the higher incidence of Alzheimer disease in women.
American journal of human genetics 1996;58(4):803-11.
1996: Yu C E; Oshima J; Fu Y H; Wijsman E M; Hisama F; Alisch R; Matthews S; Nakura J; Miki T; Ouais S; Martin G M; Mulligan J; Schellenberg G D
Positional cloning of the Werner's syndrome gene.
Science (New York, N.Y.) 1996;272(5259):258-62.
1996: Jarvik G; Larson E B; Goddard K; Schellenberg G D; Wijsman E M
Influence of apolipoprotein E genotype on the transmission of Alzheimer disease in a community-based sample.
American journal of human genetics 1996;58(1):191-200.
1995: Levy-Lahad E; Lahad A; Wijsman E M; Bird T D; Schellenberg G D
Apolipoprotein E genotypes and age of onset in early-onset familial Alzheimer's disease.
Annals of neurology 1995;38(4):678-80.
1995: Schellenberg G D
Genetic dissection of Alzheimer disease, a heterogeneous disorder.
Proceedings of the National Academy of Sciences of the United States of America 1995;92(19):8552-9.
1995: Levy-Lahad E; Wijsman E M; Nemens E; Anderson L; Goddard K A; Weber J L; Bird T D; Schellenberg G D
A familial Alzheimer's disease locus on chromosome 1.
Science (New York, N.Y.) 1995;269(5226):970-3.
1995: Schellenberg G D
Progress in Alzheimer's disease genetics.
Current opinion in neurology 1995;8(4):262-7.
1995: Jarvik G P; Wijsman E M; Kukull W A; Schellenberg G D; Yu C; Larson E B
Interactions of apolipoprotein E genotype, total cholesterol level, age, and sex in prediction of Alzheimer's disease: a case-control study.
Neurology 1995;45(6):1092-6.
1995: Schellenberg G D
Molecular genetics of familial Alzheimer's disease.
Arzneimittel-Forschung 1995;45(3A):418-24.
1994: Bonnycastle L L; Yu C E; Hunt C R; Trask B J; Clancy K P; Weber J L; Patterson D; Schellenberg G D
Cloning, sequencing, and mapping of the human chromosome 14 heat shock protein gene (HSPA2).
Genomics 1994;23(1):85-93.
1994: Payami H; Montee K R; Kaye J A; Bird T D; Yu C E; Wijsman E M; Schellenberg G D
Alzheimer's disease, apolipoprotein E4, and gender.
JAMA : the journal of the American Medical Association 1994;271(17):1316-7.
1994: Yu C E; Anderson L; Oshima J; Schellenberg G D
Dinucleotide repeat polymorphisms at the GSR gene.
Human molecular genetics 1994;3(1):212.
1994: Yu C E; Anderson L; Oshima J; Schellenberg G D
Dinucleotide repeat polymorphism at the FGFR1 gene.
Human molecular genetics 1994;3(1):212.
1994: Yu C E; Anderson L; Oshima J; Schellenberg G D
Dinucleotide repeat polymorphism at the D8S131 locus.
Human molecular genetics 1994;3(1):211.
1994: Hinds T R; Kukull W A; Van Belle G; Schellenberg G D; Villacres E C; Larson E B
Relationship between serum alpha 1-antichymotrypsin and Alzheimer's disease.
Neurobiology of aging 1994;15(1):21-7.
1994: Schellenberg G D
Alzheimer's disease: implications of genetic studies.
Neurobiology of aging 1994;15 Suppl 2():S141-4.
1993: Fu C W; Anderson L; Schellenberg G
Dinucleotide repeat polymorphism at the D14S294 locus.
Human molecular genetics 1993;2(10):1751.
1993: Schellenberg G D; Payami H; Wijsman E M; Orr H T; Goddard K A; Anderson L; Nemens E; White J A; Alonso M E; Ball M J
Chromosome 14 and late-onset familial Alzheimer disease (FAD).
American journal of human genetics 1993;53(3):619-28.
1993: Payami H; Kaye J; Heston L L; Bird T D; Schellenberg G D
Apolipoprotein E genotype and Alzheimer's disease.
Lancet 1993;342(8873):738.
1993: Wijsman E M; Bird T D; Martin G M; Schellenberg G D
The Seattle Alzheimer's disease data set.
Genetic epidemiology 1993;10(6):365-9.
1992: Schellenberg G D; Bird T D; Wijsman E M; Orr H T; Anderson L; Nemens E; White J A; Bonnycastle L; Weber J L; Alonso M E
Genetic linkage evidence for a familial Alzheimer's disease locus on chromosome 14.
Science (New York, N.Y.) 1992;258(5082):668-71.
1992: Kukull W A; Hinds T R; Schellenberg G D; van Belle G; Larson E B
Increased platelet membrane fluidity as a diagnostic marker for Alzheimer's disease: a test in population-based cases and controls.
Neurology 1992;42(3 Pt 1):607-14.
1992: Schellenberg G D; Boehnke M; Wijsman E M; Moore D K; Martin G M; Bird T D
Genetic association and linkage analysis of the apolipoprotein CII locus and familial Alzheimer's disease.
Annals of neurology 1992;31(2):223-7.
1992: Schellenberg G D; Kamino K; Bryant E M; Moore D; Bird T D
Genetic heterogeneity, Down syndrome, and Alzheimer disease.
Progress in clinical and biological research 1992;379():215-26.
1991: Schellenberg G D; Anderson L; O'dahl S; Wisjman E M; Sadovnick A D; Ball M J; Larson E B; Kukull W A; Martin G M; Roses A D
APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease.
American journal of human genetics 1991;49(3):511-7.
1991: Hsiao K K; Cass C; Schellenberg G D; Bird T; Devine-Gage E; Wisniewski H; Prusiner S B
A prion protein variant in a family with the telencephalic form of Gerstmann-Sträussler-Scheinker syndrome.
Neurology 1991;41(5):681-4.
1991: Schellenberg G D; Pericak-Vance M A; Wijsman E M; Moore D K; Gaskell P C; Yamaoka L A; Bebout J L; Anderson L; Welsh K A; Clark C M
Linkage analysis of familial Alzheimer disease, using chromosome 21 markers.
American journal of human genetics 1991;48(3):563-83.
1990: Eto K; Sumi S M; Bird T D; McEvoy-Bush T; Boehnke M; Schellenberg G
Family with dominantly inherited ataxia, amyotrophy, and peripheral sensory loss. Spinopontine atrophy or Machado-Joseph Azorean disease in another non-Portuguese family?
Archives of neurology 1990;47(9):968-74.
1990: Martin G M; Schellenberg G D; Wijsman E M; Bird T D
Alzheimer's disease. Dominant susceptibility genes.
Nature 1990;347(6289):124.
1989: Bird T D; Schellenberg G D; Wijsman E M; Martin G M
Evidence for etiologic heterogeneity in Alzheimer's disease.
Neurobiology of aging 1989;10(5):432-4; discussion 446-8.
1989: Bird T D; Sumi S M; Nemens E J; Nochlin D; Schellenberg G; Lampe T H; Sadovnick A; Chui H; Miner G W; Tinklenberg J
Phenotypic heterogeneity in familial Alzheimer's disease: a study of 24 kindreds.
Annals of neurology 1989;25(1):12-25.
1989: Bird T D; Lampe T H; Nemens E J; Sumi S M; Nochlin D; Schellenberg G D; Wijsman E M
Characteristics of familial Alzheimer's disease in nine kindreds of Volga German ancestry.
Progress in clinical and biological research 1989;317():229-34.
1989: Schellenberg G D; Bird T D; Wijsman E M; Moore D K; Martin G M
The genetics of Alzheimer's disease.
Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie 1989;43(7):463-8.
1988: Schellenberg G D; Bird T D; Wijsman E M; Moore D K; Boehnke M; Bryant E M; Lampe T H; Nochlin D; Sumi S M; Deeb S S
Absence of linkage of chromosome 21q21 markers to familial Alzheimer's disease.
Science (New York, N.Y.) 1988;241(4872):1507-10.
1988: Bird T D; Lampe T H; Nemens E J; Miner G W; Sumi S M; Schellenberg G D
Familial Alzheimer's disease in American descendants of the Volga Germans: probable genetic founder effect.
Annals of neurology 1988;23(1):25-31.
1987: Schellenberg G D; Deeb S S; Boehnke M; Bryant E M; Martin G M; Lampe T H; Bird T D
Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type.
Journal of neurogenetics 1987;4(2-3):97-108.
1987: Bird T D; Boehnke M; Schellenberg G D; Deeb S S; Lipe H P
The use of apolipoprotein CII as a genetic marker for myotonic dystrophy.
Archives of neurology 1987;44(3):273-5.
1987: Bird T D; Boehnke M; Anderson J; Lampe T H; Schellenberg G; Larson E B
The frequency of C4B variants of complement in familial and sporadic Alzheimer disease.
Alzheimer disease and associated disorders 1987;1(4):251-5.
1985: Schellenberg G D; Anderson L; Cragoe E J; Swanson P D
Inhibition of brain mitochondrial Ca2+ transport by amiloride analogues.
Cell calcium 1985;6(5):431-47.
1985: Schellenberg G D; Anderson L; Cragoe E J; Swanson P D
Inhibition of synaptosomal membrane Na+-Ca2+ exchange transport by amiloride and amiloride analogues.
Molecular pharmacology 1985;27(5):537-43.
1983: Schellenberg G D; Anderson L; Swanson P D
Inhibition of Na+-Ca2+ exchange in rat brain by amiloride.
Molecular pharmacology 1983;24(2):251-8.
1982: Schellenberg G D; Swanson P D
Solubilization and reconstitution of membranes containing the Na+ -Ca2+ exchange carrier from rat brain.
Biochimica et biophysica acta 1982;690(1):133-44.
1981: Schellenberg G D; Swanson P D
Sodium-dependent and calcium-dependent calcium transport by rat brain microsomes.
Biochimica et biophysica acta 1981;648(1):13-27.

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