Works by Pericak-Vance, Margaret A.

Results: 467

Polygenic Risk Score for Alzheimer's Disease in Caribbean Hispanics.

Published in:

2021

By:

Sariya, Sanjeev;
Felsky, Daniel;
Reyes‐Dumeyer, Dolly;
Lali, Ricky;
Lantigua, Rafael A.;
Vardarajan, Badri;
Jiménez‐Velázquez, Ivonne Z.;
Haines, Jonathan L.;
Shellenberg, Gerard D.;
Pericak‐Vance, Margaret A;
Paré, Guillaume;
Mayeux, Richard;
Tosto, Giuseppe;
Reyes-Dumeyer, Dolly;
Jiménez-Velázquez, Ivonne Z;
Pericak-Vance, Margaret A

Publication type:

journal article

Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder.

Published in:

Neurogenetics, 2018, v. 19, n. 1, p. 17, doi. 10.1007/s10048-017-0529-1

By:

Griswold, Anthony J.;
Van Booven, Derek;
Cuccaro, Michael L.;
Haines, Jonathan L.;
Gilbert, John R.;
Pericak-Vance, Margaret A.

Publication type:

Article

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.

Published in:

Neurogenetics, 2010, v. 11, n. 3, p. 291, doi. 10.1007/s10048-009-0228-7

By:

Cukier, Holly;
Rabionet, Raquel;
Konidari, Ioanna;
Rayner-Evans, Melissa;
Baltos, Mary;
Wright, Harry;
Abramson, Ruth;
Martin, Eden;
Cuccaro, Michael;
Pericak-Vance, Margaret;
Gilbert, John

Publication type:

Article

Complex gene–gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes.

Published in:

Neurogenetics, 2007, v. 8, n. 1, p. 11, doi. 10.1007/s10048-006-0058-9

By:

Motsinger, Alison;
Brassat, David;
Caillier, Stacy;
Erlich, Henry;
Walker, Karen;
Steiner, Lori;
Barcellos, Lisa;
Pericak-Vance, Margaret;
Schmidt, Silke;
Gregory, Simon;
Hauser, Stephen;
Haines, Jonathan;
Oksenberg, Jorge;
Ritchie, Marylyn

Publication type:

Article

Investigation of autism and GABA receptor subunit genes in multiple ethnic groups.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 167, doi. 10.1007/s10048-006-0045-1

By:

Collins, Ann L.;
Deqiong Ma;
Whitehead, Patrice L.;
Martin, Eden R.;
Wright, Harry H.;
Abramson, Ruth K.;
Hussman, John P.;
Haines, Jonathan L.;
Cuccaro, Michael L.;
Gilbert, John R.;
Pericak-Vance, Margaret A.

Publication type:

Article

Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis.

Published in:

Neurogenetics, 2006, v. 7, n. 3, p. 157, doi. 10.1007/s10048-006-0047-z

By:

Ping-I Lin;
Martin, Eden R.;
Browning-Large, Carrie A.;
Schmechel, Donald E.;
Welsh-Bohmer, Kathleen A.;
Murali Doraiswamy, P.;
Gilbert, John R.;
Haines, Jonathan L.;
Pericak-Vance, Margaret A.

Publication type:

Article

A new locus for dominant hereditary spastic paraplegia maps to chromosome 2p12.

Published in:

2006

By:

Züchner, Stephan;
Kail, Melanie E.;
Nance, Martha A.;
Gaskell, Perry C.;
Svenson, Ingrid K.;
Marchuk, Douglas A.;
Pericak-Vance, Margaret A.;
Ashley-Koch, Allison E.

Publication type:

Letter

Subcellular localization of spastin: implications for the pathogenesis of hereditary spastic paraplegia.

Published in:

Neurogenetics, 2005, v. 6, n. 3, p. 135, doi. 10.1007/s10048-005-0219-2

By:

Svenson, Ingrid K.;
Kloos, Mark T.;
Jacon, Amy;
Gallione, Carol;
Horton, April C.;
Pericak-Vance, Margaret A.;
Ehlers, Michael D.;
Marchuk, Douglas A.

Publication type:

Article

Comprehensive association analysis ofAPOEregulatory region polymorphisms in Alzheimer disease.

Published in:

Neurogenetics, 2004, v. 5, n. 4, p. 201, doi. 10.1007/s10048-004-0189-9

By:

Nicodemus, Kristin K.;
Stenger, Judith E.;
Schmechel, Donald E.;
Welsh-Bohmer, Kathleen A.;
Saunders, Ann M.;
Roses, Allen D.;
Gilbert, John R.;
Vance, Jeffery M.;
Haines, Jonathan L.;
Pericak-Vance, Margaret A.;
Martin, Eden R.

Publication type:

Article

Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosis.

Published in:

Neurogenetics, 2004, v. 5, n. 4, p. 209, doi. 10.1007/s10048-004-0193-0

By:

Yi-Ju Li;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.;
Siddique, Nailah;
McKenna-Yasek, Diane;
Wu-Yen Hung;
Sapp, Peter;
Allen, Coy I.;
Wenjie Chen;
Hosler, Betsy;
Saunders, Ann M.;
Dellefave, Lisa M.;
Brown, Robert H.;
Siddique, Teepu

Publication type:

Article

Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study.

Published in:

Neurogenetics, 2004, v. 5, n. 1, p. 45, doi. 10.1007/s10048-003-0163-y

By:

Pericak-Vance, Margaret A.;
Rimmler, Jackie B.;
Haines, Jonathan L.;
Garcia, Melissa E.;
Oksenberg, Jorge R.;
Barcellos, Lisa F.;
Lincoln, Robin;
Hauser, Stephen L.;
Cournu-Rebeix, Isabelle;
Azoulay-Cayla, Ariele;
Lyon-Caen, Olivier;
Fontaine, Bertrand;
Duhamel, Emmanuelle;
Coppin, Helene;
Brassat, David;
Roth, Marie-Paule;
Clanet, Michel;
Alizadeh, Mehdi;
Yaouanq, Jacqueline;
Quelvennec, Erwann

Publication type:

Article

Intragenic modifiers of hereditary spastic paraplegia due to spastin gene mutations.

Published in:

Neurogenetics, 2004, v. 5, n. 3, p. 157, doi. 10.1007/s10048-004-0186-z

By:

Svenson, Ingrid K.;
Kloos, Mark T.;
Gaskell, P. Craig;
Nance, Martha A.;
Garbern, James Y.;
Hisanaga, Shin-ichi;
Pericak-Vance, Margaret A.;
Ashley-Koch, Allison E.;
Marchuk, Douglas A.

Publication type:

Article

Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.

Published in:

Neurogenetics, 2004, v. 5, n. 3, p. 147, doi. 10.1007/s10048-004-0180-5

By:

Oliveira, Sofia A.;
Scott, William K.;
Fengyu Zhang;
Stajich, Jeffrey M.;
Fujiwara, Kenichiro;
Hauser, Michael;
Scott, Burton L.;
Pericak-Vance, Margaret A.;
Vance, Jeffrey M.;
Martin, Eden R.

Publication type:

Article

Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasis.

Published in:

Genetic Epidemiology, 2008, v. 32, n. 3, p. 187, doi. 10.1002/gepi.20294

By:

Thornton-Wells, Tricia A.;
Moore, Jason H.;
Martin, Eden R.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.

Publication type:

Article

Life After the Screen: Making Sense of Many P-Values.

Published in:

Genetic Epidemiology, 2001, v. 21, p. S546, doi. 10.1002/gepi.2001.21.s1.s546

By:

Schmidt, Silke;
Shao, Yujun;
Hauser, Elizabeth R.;
Slifer, Susan H.;
Martin, Eden R.;
Scott, William K.;
Speer, Marcy C.;
Pericak-Vance, Margaret A.

Publication type:

Article

False positive rates in a genomic screen for complex quantitative traits.

Published in:

Genetic Epidemiology, 1997, v. 14, n. 6, p. 891, doi. 10.1002/(SICI)1098-2272(1997)14:6<891::AID-GEPI55>3.0.CO;2-H

By:

Scott, William K.;
Speer, Marcy C.;
Leal, Suzanne M.;
Brzustowicz, Linda M.;
Haynes, Carol S.;
Pericak-Vance, Margaret A.

Publication type:

Article

Preface.

Published in:

Genetic Epidemiology, 1993, v. 10, n. 6, p. xix, doi. 10.1002/gepi.1370100602

By:

Elston, Robert C.;
Spence, M. Anne;
Haines, Jonathan L.;
Marazita, Mary L.;
Pericak-Vance, Margaret A.;
Siervogel, Roger M.;
MacCluer, Jean W.

Publication type:

Article

Genomic convergence to identify candidate genes for Alzheimer Disease on chromosome 10.

Published in:

Human Mutation, 2009, v. 30, n. 3, p. 463, doi. 10.1002/humu.20953

By:

Liang, Xueying;
Slifer, Michael;
Martin, Eden R.;
Schnetz-Boutaud, Nathalie;
Bartlett, Jackie;
Anderson, Brent;
Züchner, Stephan;
Gwirtsman, Harry;
Gilbert, John R.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.

Publication type:

Article

Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease.

Published in:

Human Mutation, 2007, v. 28, n. 11, p. 1065, doi. 10.1002/humu.20567

By:

Liang, Xueying;
Martin, Eden R.;
Schnetz-Boutaud, Nathalie;
Bartlett, Jackie;
Anderson, Brent;
Züchner, Stephan;
Gwirtsman, Harry;
Schmechel, Don;
Carney, Regina;
Gilbert, John R.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.

Publication type:

Article

Linkage to a known gene but no mutation identified: comprehensive reanalysis of SPG4 HSP pedigrees reveals large deletions as the sole cause.

Published in:

Human Mutation, 2007, v. 28, n. 7, p. 739, doi. 10.1002/humu.20508

By:

Beetz, Christian;
Zuchner, Stephan;
Ashley-Koch, Allison;
Auer-Grumbach, Michaela;
Byrne, Paula;
Chinnery, Patrick F.;
Hutchinson, Michael;
McDermott, Christopher J.;
Meijer, Inge A.;
Nygren, Anders O.H.;
Pericak-Vance, Margaret;
Pyle, Angela;
Rouleau, Guy A.;
Schickel, Jörg;
Shaw, Pamela J.;
Deufel, Thomas

Publication type:

Article

Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.

Published in:

Nature, 1985, v. 316, n. 6031, p. 842, doi. 10.1038/316842a0

By:

Monaco, Anthony P.;
Bertelson, Corlee J.;
Middlesworth, William;
Colletti, Chris-Anne;
Aldridge, John;
Fischbeck, Kenneth H.;
Bartlett, Richard;
Pericak-Vance, Margaret A.;
Roses, Allen D.;
Kunkel, Louis M.

Publication type:

Article

Association Analysis of Chromosome 15 GABAA Receptor Subunit Genes in Autistic Disorder.

Published in:

Journal of Neurogenetics, 2001, v. 15, n. 3/4, p. 245, doi. 10.3109/01677060109167380

By:

Menold, Marisa M.;
Shao, Yujun;
Wolpert, Chantelle M.;
Donnelly, Shannon L.;
Raiford, Kimberly L.;
Martin, Eden R.;
Ravan, Sarah A.;
Abramson, Ruth K.;
Wright, Harry H.;
Delong, G. Robert;
Cuccaro, Michael L.;
Pericak-Vance, Margaret A.;
Gilbert, John R.

Publication type:

Article

Polygenic risk score penetrance & recurrence risk in familial Alzheimer disease.

Published in:

Annals of Clinical & Translational Neurology, 2023, v. 10, n. 5, p. 744, doi. 10.1002/acn3.51757

By:

Qiao, Min;
Lee, Annie J.;
Reyes‐Dumeyer, Dolly;
Tosto, Giuseppe;
Faber, Kelley;
Goate, Alison;
Renton, Alan;
Chao, Michael;
Boeve, Brad;
Cruchaga, Carlos;
Pericak‐Vance, Margaret;
Haines, Jonathan L.;
Rosenberg, Roger;
Tsuang, Debby;
Sweet, Robert A.;
Bennett, David A.;
Wilson, Robert S.;
Foroud, Tatiana;
Mayeux, Richard;
Vardarajan, Badri N.

Publication type:

Article

F-box/ LRR-repeat protein 7 is genetically associated with Alzheimer's disease.

Published in:

Annals of Clinical & Translational Neurology, 2015, v. 2, n. 8, p. 810, doi. 10.1002/acn3.223

By:

Tosto, Giuseppe;
Fu, Hongjun;
Vardarajan, Badri N.;
Lee, Joseph H.;
Cheng, Rong;
Reyes‐Dumeyer, Dolly;
Lantigua, Rafael;
Medrano, Martin;
Jimenez‐Velazquez, Ivonne Z.;
Elkind, Mitchell S. V.;
Wright, Clinton B.;
Sacco, Ralph L.;
Pericak‐Vance, Margaret;
Farrer, Lindsay;
Rogaeva, Ekaterina;
St George‐Hyslop, Peter;
Reitz, Christiane;
Mayeux, Richard

Publication type:

Article

Associations of Sex, Race, and Apolipoprotein E Alleles With Multiple Domains of Cognition Among Older Adults.

Published in:

JAMA Neurology, 2023, v. 80, n. 9, p. 929, doi. 10.1001/jamaneurol.2023.2169

By:

Walters, Skylar;
Contreras, Alex G.;
Eissman, Jaclyn M.;
Mukherjee, Shubhabrata;
Lee, Michael L.;
Choi, Seo-Eun;
Scollard, Phoebe;
Trittschuh, Emily H.;
Mez, Jesse B.;
Bush, William S.;
Kunkle, Brian W.;
Naj, Adam C.;
Peterson, Amalia;
Gifford, Katherine A.;
Cuccaro, Michael L.;
Cruchaga, Carlos;
Pericak-Vance, Margaret A.;
Farrer, Lindsay A.;
Wang, Li-San;
Haines, Jonathan L.

Publication type:

Article

Early-Onset Alzheimer Disease and Candidate Risk Genes Involved in Endolysosomal Transport.

Published in:

JAMA Neurology, 2017, v. 74, n. 9, p. 1113, doi. 10.1001/jamaneurol.2017.1518

By:

Kunkle, Brian W.;
Vardarajan, Badri N.;
Naj, Adam C.;
Whitehead, Patrice L.;
Rolati, Sophie;
Slifer, Susan;
Carney, Regina M.;
Cuccaro, Michael L.;
Vance, Jeffery M.;
Gilbert, John R.;
Li-San Wang;
Farrer, Lindsay A.;
Reitz, Christiane;
Haines, Jonathan L.;
Beecham, GaryW.;
Martin, Eden R.;
Schellenberg, Gerard D.;
Mayeux, Richard P.;
Pericak-Vance, Margaret A.

Publication type:

Article

Overall Diet Quality and Age-Related Macular Degeneration.

Published in:

Ophthalmic Epidemiology, 2010, v. 17, n. 1, p. 58, doi. 10.3109/09286580903450353

By:

Montgomery, Martha P.;
Kamel, Freya;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.;
Postel, Eric A.;
Agarwal, Anita;
Richards, Marie;
Scott, William K.;
Schmidt, Silke

Publication type:

Article

The Impact of the Human Genome Project on Complex Disease.

Published in:

Genes, 2014, v. 5, n. 3, p. 518, doi. 10.3390/genes5030518

By:

Cooke Bailey, Jessica N.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.

Publication type:

Article

A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.

Published in:

2007

By:

Pillai, Sreekumar G.;
Chiano, Mathias N.;
White, Nicola J.;
Speer, Marcy;
Barnes, Kathleen C.;
Carlsen, Karin;
Gerritsen, Jorrit;
Helms, Peter;
Lenney, Warren;
Silverman, Michael;
Sly, Peter;
Sundy, John;
Tsanakas, John;
von Berg, Andrea;
Whyte, Moira;
Varsani, Shela;
Skelding, Paul;
Hauser, Michael;
Vance, Jeffery;
Pericak-Vance, Margaret

Publication type:

Correction Notice

A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 3, p. 307, doi. 10.1038/sj.ejhg.5201532

By:

Pillai, Sreekumar G.;
Chiano, Mathias N.;
White, Nicola J.;
Speer, Marcy;
Barnes, Kathleen C.;
Carlsen, Karin;
Gerritsen, Jorrit;
Helms, Peter;
Lenney, Warren;
Silverman, Michael;
Sly, Peter;
Sundy, John;
Tsanakas, John;
von Berg, Andrea;
Whyte, Moira;
Varsani, Shela;
Skelding, Paul;
Hauser, Michael;
Vance, Jeffery;
Pericak-Vance, Margaret

Publication type:

Article

A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death.

Published in:

Nature Medicine, 2014, v. 20, n. 12, p. 1452, doi. 10.1038/nm.3736

By:

Wetzel-Smith, Monica K;
Hunkapiller, Julie;
Bhangale, Tushar R;
Srinivasan, Karpagam;
Maloney, Janice A;
Atwal, Jasvinder K;
Sa, Susan M;
B Yaylaoglu, Murat;
Foreman, Oded;
Ortmann, Ward;
Rathore, Nisha;
Hansen, David V;
Tessier-Lavigne, Marc;
Mayeux, Richard;
Pericak-Vance, Margaret;
Haines, Jonathan;
Farrer, Lindsay A;
Schellenberg, Gerard D;
Goate, Alison;
Behrens, Timothy W

Publication type:

Article

Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.

Published in:

Nature Genetics, 2009, v. 41, n. 7, p. 776, doi. 10.1038/ng.401

By:

De Jager, Philip L.;
Xiaoming Jia;
Joanne Wang;
de Bakker, Paul I. W.;
Ottoboni, Linda;
Aggarwal, Neelum T.;
Piccio, Laura;
Raychaudhuri, Soumya;
Tran, Dong.;
Aubin, Cristin;
Briskin, Rebeccah;
Romano, Susan;
Baranzini, Sergio E.;
McCauley, Jacob L.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.;
Gibson, Rachel A.;
Naeglin, Yvonne;
Uitdehaag, Bernard;
Matthews, Paul M.

Publication type:

Article

Marcy Carlson Speer 1959–2007.

Published in:

2007

By:

Pericak-Vance, Margaret A.

Publication type:

Obituary

Interleukin 7 receptor α chain (IL7R) shows allelic and functional association with multiple sclerosis.

Published in:

Nature Genetics, 2007, v. 39, n. 9, p. 1083, doi. 10.1038/ng2103

By:

Gregory, Simon G.;
Schmidt, Silke;
Seth, Puneet;
Oksenberg, Jorge R.;
Hart, John;
Prokop, Angela;
Caillier, Stacy J.;
Ban, Maria;
Goris, An;
Barcellos, Lisa F.;
Lincoln, Robin;
McCauley, Jacob L.;
Sawcer, Stephen J.;
Compston, D. A. S.;
Dubois, Benedicte;
Hauser, Stephen L.;
Garcia-Blanco, Mariano A.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.

Publication type:

Article

A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.

Published in:

2006

By:

de Bakker, Paul I. W.;
McVean, Gil;
Sabeti, Pardis C.;
Miretti, Marcos M.;
Green, Todd;
Marchini, Jonathan;
Ke, Xiayi;
Monsuur, Alienke J.;
Whittaker, Pamela;
Delgado, Marcos;
Morrison, Jonathan;
Richardson, Angela;
Walsh, Emily C.;
Gao, Xiaojiang;
Galver, Luana;
Hart, John;
Hafler, David A.;
Pericak-Vance, Margaret;
Todd, John A.;
Daly, Mark J.

Publication type:

Letter

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.

Published in:

Nature Genetics, 2005, v. 37, n. 3, p. 289, doi. 10.1038/ng1514

By:

Züchner, Stephan;
Noureddine, Maher;
Kennerson, Marina;
Verhoeven, Kristien;
Claeys, Kristl;
De Jonghe, Peter;
Merory, John;
Oliveira, Sofia A.;
Speer, Marcy C.;
Stenger, Judith E.;
Walizada, Gina;
Danqing Zhu;
Pericak-Vance, Margaret A.;
Nicholson, Garth;
Timmerman, Vincent;
Vance, Jeffery M.

Publication type:

Article

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A.

Published in:

Nature Genetics, 2004, v. 36, n. 5, p. 449, doi. 10.1038/ng1341

By:

Züchner, Stephan;
Mersiyanova, Irina V;
Muglia, Maria;
Bissar-Tadmouri, Nisrine;
Rochelle, Julie;
Dadali, Elena L;
Zappia, Mario;
Nelis, Eva;
Patitucci, Alessandra;
Senderek, Jan;
Parman, Yesim;
Evgrafov, Oleg;
Jonghe, Peter De;
Takahashi, Yuji;
Tsuji, Shoij;
Pericak-Vance, Margaret A;
Quattrone, Aldo;
Battologlu, Esra;
Polyakov, Alexander V;
Timmerman, Vincent

Publication type:

Article

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.

Published in:

Nature Genetics, 2002, v. 30, n. 1, p. 21, doi. 10.1038/ng796

By:

Baxter, Rachel V.;
Ben Othmane, Kamel;
Rochelle, Julie M.;
Stajich, Jason E.;
Hulette, Christine;
Dew-Knight, Susan;
Hentati, Faycal;
Ben Hamida, Mongi;
Bel, S.;
Stenger, Judy E.;
Gilbert, John R.;
Pericak-Vance, Margaret A.;
Vance, Jeffery M.

Publication type:

Article

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.

Published in:

Nature Genetics, 2001, v. 29, n. 2, p. 160, doi. 10.1038/ng1001-160

By:

Yang, Yi;
Hentati, Afif;
Deng, Han-Xiang;
Dabbagh, Omar;
Sasaki, Toru;
Hirano, Makito;
Hung, Wu-Yen;
Ouahchi, Karim;
Yan, Jianhua;
Azim, Anser C.;
Cole, Natalie;
Gascon, Generoso;
Yagmour, Ayesha;
Ben-Hamida, Mongi;
Pericak-Vance, Margaret;
Hentati, Fayçal;
Siddique, Teepu

Publication type:

Article

PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients.

Published in:

Nature Genetics, 2001, v. 29, n. 1, p. 23, doi. 10.1038/ng722

By:

Barcellos, Lisa F.;
Caillier, Stacy;
Dragone, Leonard;
Elder, Melissa;
Vittinghoff, Eric;
Bucher, Patricia;
Lincoln, Robin R.;
Pericak-Vance, Margaret;
Haines, Jonathan L.;
Weiss, Arthur;
Hauser, Stephen L.;
Oksenberg, Jorge R.

Publication type:

Article

A conserved sorting-associated protein is mutant in chorea-acanthocytosis.

Published in:

Nature Genetics, 2001, v. 28, n. 2, p. 119, doi. 10.1038/88821

By:

Rampoldi, Luca;
Dobson-Stone, Carol;
Rubio, Justin P.;
Danek, Adrian;
Chalmers, Richard M.;
Wood, Nicholas W.;
Verellen, Christine;
Ferrer, Xavier;
Malandrini, Alessandro;
Fabrizi, Gian M.;
Brown, Robert;
Vance, Jeffery;
Pericak-Vance, Margaret;
Rudolf, Gabrielle;
Carrè, Sophie;
Alonso, Elisa;
Manfredi, Michela;
Németh, Andrea H.;
Monaco, Anthony P.

Publication type:

Article

SNPs in Multi-Species Conserved Sequences (MCS) as useful markers in association studies: a practical approach.

Published in:

BMC Genomics, 2007, v. 8, p. 266, doi. 10.1186/1471-2164-8-266

By:

McCauley, Jacob L;
Kenealy, Shannon J;
Margulies, Elliott H;
Schnetz-Boutaud, Nathalie;
Gregory, Simon G;
Hauser, Stephen L;
Oksenberg, Jorge R;
Pericak-Vance, Margaret A;
Haines, Jonathan L;
Mortlock, Douglas P

Publication type:

Article

Vitamin D from different sources is inversely associated with Parkinson disease.

Published in:

Movement Disorders, 2015, v. 30, n. 4, p. 560, doi. 10.1002/mds.26117

By:

Wang, Liyong;
Evatt, Marian L.;
Maldonado, Lizmarie G.;
Perry, William R.;
Ritchie, James C.;
Beecham, Gary W.;
Martin, Eden R.;
Haines, Jonathan L.;
Pericak‐Vance, Margaret A.;
Vance, Jeffery M.;
Scott, William K.

Publication type:

Article

Lewy body pathology is a frequent co-pathology in familial Alzheimer's disease.

Published in:

Acta Neuropathologica, 2003, v. 105, n. 5, p. 484, doi. 10.1007/s00401-003-0670-9

By:

Trembath, Yuri;
Rosenberg, Carolyn;
Ervin, John F.;
Schmechel, Donald E.;
Gaskell, Perry;
Pericak-Vance, Margaret;
Vance, Jeffery;
Hulette, Christine M.

Publication type:

Article

Author Correction: Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons.

Published in:

2022

By:

DeRosa, Brooke A.;
Hokayem, Jimmy El;
Artimovich, Elena;
Garcia-Serje, Catherine;
Phillips, Andre W.;
Van Booven, Derek;
Nestor, Jonathan E.;
Wang, Lily;
Cuccaro, Michael L.;
Vance, Jefery M.;
Pericak-Vance, Margaret A.;
Cukier, Holly N.;
Nestor, Michael W.;
Dykxhoorn, Derek M.

Publication type:

Correction Notice

Examination of Candidate Exonic Variants for Association to Alzheimer Disease in the Amish.

Published in:

PLoS ONE, 2015, v. 10, n. 2, p. 1, doi. 10.1371/journal.pone.0118043

By:

D’Aoust, Laura N.;
Cummings, Anna C.;
Laux, Renee;
Fuzzell, Denise;
Caywood, Laura;
Reinhart-Mercer, Lori;
Scott, William K.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.

Publication type:

Article

KIAA1462, A Coronary Artery Disease Associated Gene, Is a Candidate Gene for Late Onset Alzheimer Disease in APOE Carriers.

Published in:

PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0082194

By:

Murdock, Deborah G.;
Bradford, Yuki;
Schnetz-Boutaud, Nathalie;
Mayo, Ping;
Allen, Melissa J.;
D’Aoust, Laura N.;
Liang, Xueying;
Mitchell, Sabrina L.;
Zuchner, Stephan;
Small, Gary W.;
Gilbert, John R.;
Pericak-Vance, Margaret A.;
Haines, Jonathan L.

Publication type:

Article

Evaluating Power and Type 1 Error in Large Pedigree Analyses of Binary Traits

Published in:

PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0062615

By:

Cummings, Anna C.;
Torstenson, Eric;
Davis, Mary F.;
D’Aoust, Laura N.;
Scott, William K.;
Pericak-Vance, Margaret A.;
Bush, William S.;
Haines, Jonathan L.

Publication type:

Article

Copy Number Variants in Extended Autism Spectrum Disorder Families Reveal Candidates Potentially Involved in Autism Risk.

Published in:

PLoS ONE, 2011, v. 6, n. 10, p. 1, doi. 10.1371/journal.pone.0026049

By:

Salyakina, Daria;
Cukier, Holly N.;
Lee, Joycelyn M.;
Sacharow, Stephanie;
Nations, Laura D.;
Ma, Deqiong;
Jaworski, James M.;
Konidari, Ioanna;
Whitehead, Patrice L.;
Wright, Harry H.;
Abramson, Ruth K.;
Williams, Scott M.;
Menon, Ramkumar;
Haines, Jonathan L.;
Gilbert, John R.;
Cuccaro, Michael L.;
Pericak-Vance, Margaret A.

Publication type:

Article

Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform.

Published in:

PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0018595

By:

Hedges, Dale J.;
Guettouche, Toumy;
Shan Yang;
Bademci, Guney;
Diaz, Ashley;
Andersen, Ashley;
Hulme, William F.;
Linker, Sara;
Mehta, Arpit;
Edwards, Yvonne J. K.;
Beecham, Gary W.;
Martin, Eden R.;
Pericak-Vance, Margaret A.;
Zuchner, Stephan;
Vance, Jeffery M.;
Gilbert, John R.

Publication type:

Article