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Select item 111002241.

DNA Methylation Near DLGAP2 May Mediate the Relationship between Family History of Type 1 Diabetes and Type 1 Diabetes Risk

Randi K. Johnson, Amanda J. Ireton, Patrick M. Carry, Lauren A. Vanderlinden, Fran Dong, Alex Romero, David R. Johnson, Debashis Ghosh, Fan Yang, Brigitte Frohnert, Ivana V. Yang, Katerina Kechris, Marian Rewers, Jill M. Norris

Pediatr Diabetes. Author manuscript; available in PMC 2024 May 17.

Published in final edited form as: Pediatr Diabetes. 2023; 2023: 5367637. Published online 2023 Sep 11. doi: 10.1155/2023/5367637

PMCID:: PMC11100224

Abstract Article PDF–775K

Select item 75021752.

Cross-Species Analyses Identify Dlgap2 as a Regulator of Age-Related Cognitive Decline and Alzheimer’s Dementia

Andrew R. Ouellette, Sarah M. Neuner, Logan Dumitrescu, Laura C. Anderson, Daniel M. Gatti, Emily R. Mahoney, Jason A. Bubier, Gary Churchill, Luanne Peters, Matthew J. Huentelman, Jeremy H. Herskowitz, Hyun-Sik Yang, Alexandra N. Smith, Christiane Reitz, Brian W. Kunkle, Charles C. White, Philip L. De Jager, Julie A. Schneider, David A. Bennett, Nicholas T. Seyfried, Alzheimer’s Disease Genetics Consortium, Elissa J. Chesler, Niran Hadad, Timothy J. Hohman, Catherine C. Kaczorowski

Cell Rep. Author manuscript; available in PMC 2020 Sep 20.

Published in final edited form as: Cell Rep. 2020 Sep 1; 32(9): 108091. doi: 10.1016/j.celrep.2020.108091

PMCID:: PMC7502175

Abstract Article PDF–1.2M

Select item 69616563.

Cannabis use is associated with potentially heritable widespread changes in autism candidate gene DLGAP2 DNA methylation in sperm

Rose Schrott, Kelly Acharya, Nilda Itchon-Ramos, Andrew B. Hawkey, Erica Pippen, John T. Mitchell, Scott H. Kollins, Edward D. Levin, Susan K. Murphy

Epigenetics. 2020; 15(1-2): 161–173. Published online 2019 Aug 26. doi: 10.1080/15592294.2019.1656158

PMCID:: PMC6961656

Abstract Article PDF–1.4M

Select item 62694604.

Quantitative DNA Methylation Analysis of DLGAP2 Gene using Pyrosequencing in Schizophrenia with Tardive Dyskinesia: A Linear Mixed Model Approach

Yanli Li, Kesheng Wang, Ping Zhang, Junchao Huang, Huimei An, Nianyang Wang, Fu De Yang, Zhiren Wang, Shuping Tan, Song Chen, Yunlong Tan

Sci Rep. 2018; 8: 17466. Published online 2018 Nov 30. doi: 10.1038/s41598-018-35718-4

PMCID:: PMC6269460

Abstract Article PDF–1.0M

Select item 45523255.

Glutamate System Genes and Brain Volume Alterations in Pediatric Obsessive-Compulsive Disorder: A Preliminary Study

Ke Wu, Gregory L. Hanna, Philip Easter, James L. Kennedy, David R. Rosenberg, Paul D Arnold

Psychiatry Res. Author manuscript; available in PMC 2015 Aug 28.

Published in final edited form as: Psychiatry Res. 2013 Mar 30; 211(3): 214–220. Published online 2012 Nov 13. doi: 10.1016/j.pscychresns.2012.07.003

PMCID:: PMC4552325

Abstract Article PDF–314K

Select item 38857126.

Role of the DLGAP2 Gene Encoding the SAP90/PSD-95-Associated Protein 2 in Schizophrenia

Jun-Ming Li, Chao-Lin Lu, Min-Chih Cheng, Sy-Ueng Luu, Shih-Hsin Hsu, Tsung-Ming Hu, Hsin-Yao Tsai, Chia-Hsiang Chen

PLoS One. 2014; 9(1): e85373. Published online 2014 Jan 8. doi: 10.1371/journal.pone.0085373

PMCID:: PMC3885712

Abstract Article PDF–538K

Select item 20995817.

Computational and experimental identification of novel human imprinted genes

Philippe P. Luedi, Fred S. Dietrich, Jennifer R. Weidman, Jason M. Bosko, Randy L. Jirtle, Alexander J. Hartemink

Genome Res. 2007 Dec; 17(12): 1723–1730. doi: 10.1101/gr.6584707

PMCID:: PMC2099581

Abstract Article PDF–433K

Select item 43243558.

Genetic Variation in Imprinted Genes is Associated with Risk of Late-Onset Alzheimer’s disease

Mamoonah Chaudhry, Xingbin Wang, Mikhil N. Bamne, Shahida Hasnain, F.Yesim Demirci, Oscar L. Lopez, M. Ilyas Kamboh

J Alzheimers Dis. Author manuscript; available in PMC 2016 Jan 1.

Published in final edited form as: J Alzheimers Dis. 2015 Jan 1; 44(3): 989–994. doi: 10.3233/JAD-142106

PMCID:: PMC4324355

Abstract Article PDF–507K

Select item 30217989.

Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder

Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R. Magalhaes, Catarina Correia, Brett S. Abrahams, Joana Almeida, Elena Bacchelli, Gary D. Bader, Anthony J. Bailey, Gillian Baird, Agatino Battaglia, Tom Berney, Nadia Bolshakova, Sven Bölte, Patrick F. Bolton, Thomas Bourgeron, Sean Brennan, Jessica Brian, Susan E. Bryson, Andrew R. Carson, Guillermo Casallo, Jillian Casey, Lynne Cochrane, Christina Corsello, Emily L. Crawford, Andrew Crossett, Geraldine Dawson, Maretha de Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Ana Filipa, Susan E. Folstein, Eric Fombonne, Christine M. Freitag, John Gilbert, Christopher Gillberg, Joseph T. Glessner, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Hakon Hakonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer L. Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, Alexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara M. Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett L. Leventhal, Anath C. Lionel, Xiao-Qing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala K. Mirza, Jeff Munson, Stanley F. Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Katerina Papanikolaou, Jeremy R. Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Marion Pilorge, Joseph Piven, Chris P. Ponting, David J. Posey, Annemarie Poustka, Fritz Poustka, Aparna Prasad, Jiannis Ragoussis, Katy Renshaw, Jessica Rickaby, Wendy Roberts, Kathryn Roeder, Bernadette Roge, Michael L. Rutter, Laura J. Bierut, John P. Rice, SAGE Consortium, Jeff Salt, Katherine Sansom, Daisuke Sato, Ricardo Segurado, Lili Senman, Naisha Shah, Val C. Sheffield, Latha Soorya, Inês Sousa, Olaf Stein, Vera Stoppioni, Christina Strawbridge, Raffaella Tancredi, Katherine Tansey, Bhooma Thiruvahindrapduram, Ann P. Thompson, Susanne Thomson, Ana Tryfon, John Tsiantis, Herman Van Engeland, John B. Vincent, Fred Volkmar, Simon Wallace, Kai Wang, Zhouzhi Wang, Thomas H. Wassink, Caleb Webber, Kirsty Wing, Kerstin Wittemeyer, Shawn Wood, Jing Wu, Brian L. Yaspan, Danielle Zurawiecki, Lonnie Zwaigenbaum, Joseph D. Buxbaum, Rita M. Cantor, Edwin H. Cook, Hilary Coon, Michael L. Cuccaro, Bernie Devlin, Sean Ennis, Louise Gallagher, Daniel H. Geschwind, Michael Gill, Jonathan L. Haines, Joachim Hallmayer, Judith Miller, Anthony P. Monaco, John I. Nurnberger, Jr., Andrew D. Paterson, Margaret A. Pericak-Vance, Gerard D. Schellenberg, Peter Szatmari, Astrid M. Vicente, Veronica J. Vieland, Ellen M. Wijsman, Stephen W. Scherer, James S. Sutcliffe, Catalina Betancur

Nature. Author manuscript; available in PMC 2011 Jan 16.

Published in final edited form as: Nature. 2010 Jul 15; 466(7304): 368–372. Published online 2010 Jun 9. doi: 10.1038/nature09146

PMCID:: PMC3021798

Abstract Article PDF–458K

Select item 118061210.

Slowed Conduction and Thin Myelination of Peripheral Nerves Associated with Mutant Rho Guanine-Nucleotide Exchange Factor 10

Kristien Verhoeven, Peter De Jonghe, Tom Van de Putte, Eva Nelis, An Zwijsen, Nathalie Verpoorten, Els De Vriendt, An Jacobs, Veerle Van Gerwen, Annick Francis, Chantal Ceuterick, Danny Huylebroeck, Vincent Timmerman

Am J Hum Genet. 2003 Oct; 73(4): 926–932. Published online 2003 Aug 19. doi: 10.1086/378159

PMCID:: PMC1180612

Abstract Article PDF–670K

Select item 372331211.

Genome-wide association study of age at menarche in African-American women

Ellen W. Demerath, Ching-Ti Liu, Nora Franceschini, Gary Chen, Julie R. Palmer, Erin N. Smith, Christina T.L. Chen, Christine B. Ambrosone, Alice M. Arnold, Elisa V. Bandera, Gerald S. Berenson, Leslie Bernstein, Angela Britton, Anne R. Cappola, Christopher S. Carlson, Stephen J. Chanock, Wei Chen, Zhao Chen, Sandra L. Deming, Cathy E. Elks, Michelle K. Evans, Zofia Gajdos, Brian E. Henderson, Jennifer J. Hu, Sue Ingles, Esther M. John, Kathleen F. Kerr, Laurence N. Kolonel, Loic Le Marchand, Xiaoning Lu, Robert C. Millikan, Solomon K. Musani, Nora L. Nock, Kari North, Sarah Nyante, Michael F. Press, Jorge L. Rodriquez-Gil, Edward A. Ruiz-Narvaez, Nicholas J. Schork, Sathanur R. Srinivasan, Nancy F. Woods, Wei Zheng, Regina G. Ziegler, Alan Zonderman, Gerardo Heiss, B. Gwen Windham, Melissa Wellons, Sarah S. Murray, Michael Nalls, Tomi Pastinen, Aleksandar Rajkovic, Joel Hirschhorn, L. Adrienne Cupples, Charles Kooperberg, Joanne M. Murabito, Christopher A. Haiman

Hum Mol Genet. 2013 Aug 15; 22(16): 3329–3346. Published online 2013 Apr 17. doi: 10.1093/hmg/ddt181

PMCID:: PMC3723312

Abstract Article PDF–818K

Select item 406207112.

Amerindian-specific regions under positive selection harbour new lipid variants in Latinos

Arthur Ko, Rita M. Cantor, Daphna Weissglas-Volkov, Elina Nikkola, Prasad M. V. Linga Reddy, Janet S. Sinsheimer, Bogdan Pasaniuc, Robert Brown, Marcus Alvarez, Alejandra Rodriguez, Rosario Rodriguez-Guillen, Ivette C. Bautista, Olimpia Arellano-Campos, Linda L. Muñoz-Hernández, Veikko Salomaa, Jaakko Kaprio, Antti Jula, Matti Jauhiainen, Markku Heliövaara, Olli Raitakari, Terho Lehtimäki, Johan G. Eriksson, Markus Perola, Kirk E. Lohmueller, Niina Matikainen, Marja-Riitta Taskinen, Maribel Rodriguez-Torres, Laura Riba, Teresa Tusie-Luna, Carlos A. Aguilar-Salinas, Päivi Pajukanta

Nat Commun. 2014 Jun 2; 5: 3983. Published online 2014 Jun 2. doi: 10.1038/ncomms4983

PMCID:: PMC4062071

Abstract Article PDF–821K

Select item 295884413.

Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardation

Audrey Guilmatre, Christèle Dubourg, Anne-Laure Mosca, Solenn Legallic, Alice Goldenberg, Valérie Drouin-Garraud, Valérie Layet, Antoine Rosier, Sylvain Briault, Frédérique Bonnet-Brilhault, Frédéric Laumonnier, Sylvie Odent, Gael Le Vacon, Géraldine Joly-Helas, Véronique David, Claude Bendavid, Jean-Michel Pinoit, Céline Henry, Caterina Impallomeni, Eva Germano, Gaetano Tortorella, Gabriella Di Rosa, Catherine Barthelemy, Christian Andres, Laurence Faivre, Thierry Frébourg, Pascale Saugier Veber, Dominique Campion

Arch Gen Psychiatry. Author manuscript; available in PMC 2010 Oct 25.

Published in final edited form as: Arch Gen Psychiatry. 2009 Sep; 66(9): 947–956. doi: 10.1001/archgenpsychiatry.2009.80

PMCID:: PMC2958844

Abstract Article

Select item 399653714.

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism

Roser Corominas, Xinping Yang, Guan Ning Lin, Shuli Kang, Yun Shen, Lila Ghamsari, Martin Broly, Maria Rodriguez, Stanley Tam, Shelly A. Wanamaker, Changyu Fan, Song Yi, Murat Tasan, Irma Lemmens, Xingyan Kuang, Nan Zhao, Dheeraj Malhotra, Jacob J. Michaelson, Vladimir Vacic, Michael A. Calderwood, Frederick P. Roth, Jan Tavernier, Steve Horvath, Kourosh Salehi-Ashtiani, Dmitry Korkin, Jonathan Sebat, David E. Hill, Tong Hao, Marc Vidal, Lilia M. Iakoucheva

Nat Commun. 2014; 5: 3650. Published online 2014 Apr 11. doi: 10.1038/ncomms4650

Correction in:: Nat Commun. 2023; 14: 569.

PMCID:: PMC3996537

Abstract Article PDF–1.9M

Select item 876907215.

Proteome‐scale mapping of binding sites in the unstructured regions of the human proteome

Caroline Benz, Muhammad Ali, Izabella Krystkowiak, Leandro Simonetti, Ahmed Sayadi, Filip Mihalic, Johanna Kliche, Eva Andersson, Per Jemth, Norman E Davey, Ylva Ivarsson

Mol Syst Biol. 2022 Jan; 18(1): e10584. Published online 2022 Jan 19. doi: 10.15252/msb.202110584

PMCID:: PMC8769072

Abstract Article PDF–2.9M

Select item 631495716.

An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders

Siwei Chen, Robert Fragoza, Lambertus Klei, Yuan Liu, Jiebiao Wang, Kathryn Roeder, Bernie Devlin, Haiyuan Yu

Nat Genet. Author manuscript; available in PMC 2019 Jul 1.

Published in final edited form as: Nat Genet. 2018 Jul; 50(7): 1032–1040. Published online 2018 Jun 11. doi: 10.1038/s41588-018-0130-z

PMCID:: PMC6314957

Abstract Article PDF–1.3M

Select item 316943217.

Protein interactome reveals converging molecular pathways among autism disorders

Yasunari Sakai, Chad A. Shaw, Brian C. Dawson, Diana V. Dugas, Zaina Al-Mohtaseb, David E. Hill, Huda Y. Zoghbi

Sci Transl Med. Author manuscript; available in PMC 2011 Dec 8.

Published in final edited form as: Sci Transl Med. 2011 Jun 8; 3(86): 86ra49. doi: 10.1126/scitranslmed.3002166

PMCID:: PMC3169432

Abstract Article PDF–6.0M

Select item 294516818.

Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study

Swneke D. Bailey, Changchun Xie, Ron Do, Alexandre Montpetit, Rafael Diaz, Viswanathan Mohan, Bernard Keavney, Salim Yusuf, Hertzel C. Gerstein, James C. Engert, Sonia Anand, on behalf of the DREAM investigators

Diabetes Care. 2010 Oct; 33(10): 2250–2253. Published online 2010 Jul 13. doi: 10.2337/dc10-0452

PMCID:: PMC2945168

Abstract Article PDF–153K

Select item 277583219.

Gene-centric Association Signals for Lipids and Apolipoproteins Identified via the HumanCVD BeadChip

Philippa J. Talmud, Fotios Drenos, Sonia Shah, Tina Shah, Jutta Palmen, Claudio Verzilli, Tom R. Gaunt, Jacky Pallas, Ruth Lovering, Kawah Li, Juan Pablo Casas, Reecha Sofat, Meena Kumari, Santiago Rodriguez, Toby Johnson, Stephen J. Newhouse, Anna Dominiczak, Nilesh J. Samani, Mark Caulfield, Peter Sever, Alice Stanton, Denis C. Shields, on behalf of the ASCOT investigators, Sandosh Padmanabhan, Olle Melander, Claire Hastie, Christian Delles, on behalf of the NORDIL investigators, Shah Ebrahim, Michael G. Marmot, George Davey Smith, Debbie A. Lawlor, Patricia B. Munroe, for the BRIGHT Consortium, Ian N. Day, Mika Kivimaki, John Whittaker, Steve E. Humphries, Aroon D. Hingorani

Am J Hum Genet. 2009 Nov 13; 85(5): 628–642. doi: 10.1016/j.ajhg.2009.10.014

PMCID:: PMC2775832

Abstract Article PDF–2.8M

Select item 289646420.

Personalized Smoking Cessation: Interactions between Nicotine Dose, Dependence and Quit-Success Genotype Score

Jed E Rose, Frédérique M Behm, Tomas Drgon, Catherine Johnson, George R Uhl

Mol Med. 2010 Jul-Aug; 16(7-8): 247–253. Published online 2010 Mar 17. doi: 10.2119/molmed.2009.00159

Correction in:: Mol Med. 2012; 18(1): 729.

PMCID:: PMC2896464

Abstract Article PDF–2.4M

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