Michael L. Cuccaro
Active 1995–2025
- 83
- Papers
- 18,123
- Citations
- 52
- h-index
- 72
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Biochemistry, Genetics and Molecular Biology40.4%
- Neuroscience34.9%
- Medicine15.9%
- Psychology5.8%
- Computer Science0.5%
- Social Sciences0.5%
- Other2%
Topics
- Autism Spectrum Disorder Research12.6%
- Genetics and Neurodevelopmental Disorders10.6%
- Genomic variations and chromosomal abnormalities4.1%
- Alzheimer's disease research and treatments3.9%
- Genetic Associations and Epidemiology3.6%
- Genomics and Rare Diseases2.8%
- Other62.4%
Coauthors
- Margaret A. Pericak‐Vance53
- Jeffery M. Vance30
- Eden R. Martin25
- John R. Gilbert25
- Jonathan L. Haines25
- Ruth K. Abramson21
- Gary W. Beecham18
- Patrice L. Whitehead18
- Harry H. Wright17
- Anthony J. Griswold15
- Farid Rajabli14
- Chantelle M. Wolpert13
- Larry D. Adams12
- Brian W. Kunkle11
- Goldie S. Byrd11
- Kara L. Hamilton‐Nelson11
- Holly N. Cukier10
- William S. Bush10
- Gerard D. Schellenberg9
- Lindsay A. Farrer9
- Pedro Mena9
- Allison E. Ashley‐Koch8
- Jesse Mez8
- Marisa M. Menold8
All papers
- New insights into the genetic etiology of Alzheimer’s disease and related dementias
Authors: Céline Bellenguez, Fahri Küçükali, Iris E. Jansen, Luca Kleineidam, Sonia Moreno–Grau, Najaf Amin, Adam C. Naj, Rafael Campos-Martín, Benjamin Grenier‐Boley, Víctor Andrade, Peter Holmans, Anne Boland, Vincent Damotte, Sven J. van der Lee, Marcos R. Costa, Teemu Kuulasmaa, Qiong Yang, Itziar de Rojas, Joshua C. Bis, Amber Yaqub, Ivana Nedeljković, Julien Chapuis, Shahzad Ahmad, Vilmantas Giedraitis, Dag Aarsland, Pablo García‐González, Carla Abdelnour, Emilio Alarcón‐Martín, Daniel Alcolea, Montserrat Alegret, Ignacio Álvarez, Victoria Álvarez, Nicola J. Armstrong, Anthoula Tsolaki, Carmen Antúnez, Ildebrando Appollonio, Marina Arcaro, Silvana Archetti, Alfonso Arias Pastor, Beatrice Arosio, Lavinia Athanasiu, Henri Bailly, Nerisa Banaj, Miquel Baquero, Sandra Barral, Alexa Beiser, Ana Belén Pastor, Jennifer E. Below, Penelope Benchek, Luisa Benussi, Claudine Berr, Céline Besse, Valentina Bessi, Giuliano Binetti, Alessandra Bizarro, Rafael Blesa, Merçé Boada, Eric Boerwinkle, Barbara Borroni, Silvia Boschi, Paola Bossù, Geir Bråthen, Jan Bressler, Catherine Bresner, Henry Brodaty, Keeley J. Brookes, Luis Ignacio Brusco, Dolores Buiza‐Rueda, Katharina Bürger, Vanessa Burholt, William S. Bush, Miguel Calero, Laura B. Cantwell, Geneviève Chêne, Jaeyoon Chung, Michael L. Cuccaro, Ãngel Carracedo, Roberta Cecchetti, Laura Cervera‐Carles, Camille Charbonnier, Hung‐Hsin Chen, Caterina Chillotti, Simona Ciccone, Jurgen A.H.R. Claassen, Christopher Clark, Elisa Conti, Anaïs Corma‐Gómez, Emanuele Maria Costantini, Carlo Custodero, Delphine Daian, Carolina Dalmasso, Antonio Daniele, Efthimios Dardiotis, Jean‐François Dartigues, Peter Paul De Deyn, Kátia de Paiva Lopes, Lot D. de Witte, Stéphanie Debette, Jürgen Deckert, Teodoro del Ser and 1,166 more - Nature Genetics 2022 cited by 2,471
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
Authors: F. Kyle Satterstrom, Jack A. Kosmicki, Jiebiao Wang, Michael S. Breen, Silvia De Rubeis, Joon‐Yong An, Minshi Peng, Ryan L. Collins, Jakob Grove, Lambertus Klei, Christine Stevens, Jennifer Reichert, Maureen Mulhern, Mykyta Artomov, Sherif Gerges, Brooke Sheppard, Xinyi Xu, Aparna Bhaduri, Utku Norman, Harrison Brand, Grace Schwartz, Rachel Nguyen, Elizabeth E. Guerrero, Caroline Dias, Branko Aleksić, Richard Anney, Mafalda Barbosa, Somer Bishop, Alfredo Brusco, Jonas Bybjerg‐Grauholm, Ãngel Carracedo, Marcus C.Y. Chan, Andreas G. Chiocchetti, Brian Hon‐Yin Chung, Hilary Coon, Michael L. Cuccaro, Aurora Currò, Bernardo Dalla Bernardina, Ryan N. Doan, Enrico Domenici, Shan Dong, Chiara Fallerini, Montse Fernández‐Prieto, Giovanni Battista Ferrero, Christine M. Freitag, Menachem Fromer, J. Jay Gargus, Daniel H. Geschwind, Elisa Giorgio, Javier González‐Peñas, Stephen J. Guter, Danielle Halpern, Emily Hansen‐Kiss, Xin He, Gail E. Herman, Irva Hertz‐Picciotto, David M. Hougaard, Christina M. Hultman, Iuliana Ionita‐Laza, Suma Jacob, Jesslyn Jamison, Astanand Jugessur, Miia Kaartinen, Gun Peggy Knudsen, A lexander Kolevzon, Itaru Kushima, So Lun Lee, Terho Lehtimäki, Elaine T. Lim, Carla Lintas, W. Ian Lipkin, Diego Lopergolo, Fátima Lopes, Yunin Ludeña, Patrı́cia Maciel, Per Magnus, Behrang Mahjani, Nell Maltman, Dara S. Manoach, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Eduarda Morgana Silva Montenegro, Danielle de Paula Moreira, Eric M. Morrow, Ole Mors, Preben Bo Mortensen, Matthew W. Mosconi, Pierandrea Muglia, Benjamin M. Neale, Merete Nordentoft, Norio Ozaki, Aarno Palotie, Mara Parellada, Maria Rita Passos‐Bueno, Margaret A. Pericak‐Vance, Antonio M. Persico, Isaac N. Pessah, Kaija Puura and 90 more - Cell 2020 cited by 2,501
- Rare coding variation provides insight into the genetic architecture and phenotypic context of autism
Authors: Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ãngel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montse Fernández‐Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, A lexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt and 17 more - Nature Genetics 2022 cited by 617
- APOE Genotype and Alzheimer Disease Risk Across Age, Sex, and Population Ancestry
Authors: Michaël E. Belloy, Shea J. Andrews, Yann Le Guen, Michael L. Cuccaro, Lindsay A. Farrer, Valerio Napolioni, Michael D. Greicius - JAMA Neurology 2023 cited by 280
- Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Authors: Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang, Jacob Vorstman, Ann Thompson, Regina Regan, Marion Pilorge, Giovanna Pellecchia, Alistair T. Pagnamenta, Bárbara Oliveira, Christian R. Marshall, Tiago R. Magalhães, Jennifer K. Lowe, Jennifer Howe, Anthony J. Griswold, John R. Gilbert, Eftichia Duketis, Beth A. Dombroski, Maretha Jonge, Michael L. Cuccaro, Emily L. Crawford, Catarina Correia, Judith Conroy, Inês C. Conceição, Andreas G. Chiocchetti, Jillian P. Casey, Guiqing Cai, Christelle Cabrol, Nadia Bolshakova, Elena Bacchelli, Richard Anney, Steven Gallinger, Michelle Cotterchio, Graham Casey, Lonnie Zwaigenbaum, Kerstin Wittemeyer, Kirsty Wing, Simon Wallace, Hermán van Engeland, Ana Tryfon, Susanne Thomson, Latha Soorya, Bernadette Rogé, Wendy Roberts, Fritz Poustka, Susana Mouga, Nancy J. Minshew, L. Alison McInnes, Susan G. McGrew, Catherine Lord, Marion Leboyer, Ann S. Couteur, A lexander Kolevzon, Patricia González, Suma Jacob, Richard Holt, Stephen J. Guter, Jonathan Green, Andrew Green, Christopher Gillberg, Bridget A. Fernandez, Frederico Duque, Richard Delorme, Géraldine Dawson, Pauline Chaste, Cátia Café, S. Brennan, Thomas Bourgeron, Patrick Bolton, Sven Bölte, Raphael Bernier, Gillian Baird, Anthony Bailey, Evdokia Anagnostou, Joana Almeida, Ellen M. Wijsman, Veronica J. Vieland, Astrid M. Vicente, Gerard D. Schellenberg, Margaret A. Pericak‐Vance, Andrew D. Paterson, Jeremy Parr, Guiomar Oliveira, John I. Nürnberger, Anthony P. Monaco, Elena Maestrini, Sabine M. Klauck, Håkon Håkonarson, Jonathan L. Haines, Daniel H. Geschwind, Christine M. Freitag, Susan E. Folstein, Sean Ennis and 12 more - The American Journal of Human Genetics 2014 cited by 1,028
- Sex differences in the genetic architecture of cognitive resilience to Alzheimer’s disease
Authors: Jaclyn M. Eissman, Logan Dumitrescu, Emily R. Mahoney, Alexandra N. Smith, Shubhabrata Mukherjee, Michael L. Lee, Phoebe Scollard, Seo Eun Choi, William S. Bush, Corinne D. Engelman, Qiongshi Lu, David W. Fardo, Emily H. Trittschuh, Jesse Mez, Catherine C. Kaczorowski, Hector Hernandez Saucedo, Keith F. Widaman, Rachel F. Buckley, Michael J Properzi, Elizabeth C. Mormino, Hyun Sik Yang, Theresa M. Harrison, Trey Hedden, Kwangsik Nho, Shea J. Andrews, Douglas Tommet, Niran Hadad, R. Elizabeth Sanders, Douglas M. Ruderfer, Katherine A. Gifford, Xiaoyuan Zhong, Neha Raghavan, Badri N. Vardarajan, The Alzheimer’s Disease Neuroimaging Initiative (ADNI), A4 Study Team, Margaret A. Pericak‐Vance, Lindsay A. Farrer, Li San Wang, Carlos Cruchaga, Gerard D. Schellenberg, Nancy J. Cox, Jonathan L. Haines, C. Dirk Keene, Andrew J. Saykin, Eric B. Larson, Reisa A. Sperling, Richard Mayeux, Michael L. Cuccaro, David A. Bennett, Julie A. Schneider, Paul K. Crane, Angela L. Jefferson, Timothy J. Hohman - Brain 2022 cited by 101
- Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations
Authors: Farid Rajabli, Briseida E. Feliciano, Katrina Celis, Kara L. Hamilton‐Nelson, Patrice L. Whitehead, Larry D. Adams, Parker L. Bussies, Clara P. Manrique, Alejandra Rodríguez, Vanessa Rodríguez, Takiyah D. Starks, Grace Byfield, Carolina Bernal López, Jacob L. McCauley, Heriberto Acosta, Ángel Chinea, Brian W. Kunkle, Christiane Reitz, Lindsay A. Farrer, Gerard D. Schellenberg, Badri N. Vardarajan, Jeffery M. Vance, Michael L. Cuccaro, Eden R. Martin, Jonathan L. Haines, Goldie S. Byrd, Gary W. Beecham, Margaret A. Pericak‐Vance - PLoS Genetics 2018 cited by 202
- A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer’s Disease in African Ancestry
Authors: Farid Rajabli, Gary W. Beecham, Hugh C. Hendrie, Olusegun Baiyewu, Adesola Ogunniyi, Sujuan Gao, Nicholas A. Kushch, Marina Lipkin-Vasquez, Kara L. Hamilton‐Nelson, Juan I. Young, Derek M. Dykxhoorn, Karen Nuytemans, Brian W. Kunkle, Liyong Wang, Fulai Jin, Xiaoxiao Liu, Briseida E. Feliciano‐Astacio, Gerard D. Schellenberg, Clifton L. Dalgard, Anthony J. Griswold, Goldie S. Byrd, Christiane Reitz, Michael L. Cuccaro, Jonathan L. Haines, Margaret A. Pericak‐Vance, Jeffery M. Vance - PLoS Genetics 2022 cited by 63
- Cognitive domain harmonization and cocalibration in studies of older adults.
Authors: Shubhabrata Mukherjee, Seo‐Eun Choi, Michael L. Lee, Phoebe Scollard, Emily H. Trittschuh, Jesse Mez, Andrew J. Saykin, Laura E. Gibbons, R. Elizabeth Sanders, Andrew Zaman, Merilee Teylan, Walter A. Kukull, Lisa L. Barnes, David A. Bennett, Andrea Z. LaCroix, Eric B. Larson, Michael L. Cuccaro, Shannon Mercado, Logan Dumitrescu, Timothy J. Hohman, Paul K. Crane - Neuropsychology 2022 cited by 99
- Associations of Sex, Race, and Apolipoprotein E Alleles With Multiple Domains of Cognition Among Older Adults
Authors: Skylar Walters, Alex G. Contreras, Jaclyn M. Eissman, Shubhabrata Mukherjee, Michael L. Lee, Seo‐Eun Choi, Phoebe Scollard, Emily H. Trittschuh, Jesse Mez, William S. Bush, Brian W. Kunkle, Adam C. Naj, Amalia Peterson, Katherine A. Gifford, Michael L. Cuccaro, Carlos Cruchaga, Margaret A. Pericak‐Vance, Lindsay A. Farrer, Li‐San Wang, Jonathan L. Haines, Angela L. Jefferson, Walter A. Kukull, C. Dirk Keene, Andrew J. Saykin, Paul M. Thompson, Eden R. Martin, David A. Bennett, Lisa L. Barnes, Julie A. Schneider, Paul K. Crane, Timothy J. Hohman, Logan Dumitrescu, Erin L. Abner, Perrie M. Adams, Alyssa Aguirre, Marilyn Albert, Roger L. Albin, Mariet Allen, Lisa Alvarez, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig Atwood, Gayle Ayres, Robert C. Barber, Lisa L. Barnes, Sandra Barral, Jackie Bartlett, Thomas G. Beach, James T. Becker, Gary W. Beecham, Penelope Benchek, David A. Bennett, John Bertelson, Sarah Biber, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James Brewer, James R. Burke, Jeffery Burns, William S. Bush, Joseph D. Buxbaum, Goldie S. Byrd, Laura B. Cantwell, Chuanhai Cao, Cynthia M. Carlsson, Minerva M. Carrasquillo, Kwun Chuen Gary Chan, Scott Chase, Yen‐Chi Chen, Marie-Franciose Chesselet, Nathaniel A. Chin, Helena C. Chui, Jaeyoon Chung, Suzanne Craft, Paul K. Crane, Carlos Cruchaga, Michael L. Cuccaro, Jessica E. Culhane, C. Munro Cullum, Eveleen Darby, Bárbara Davis, Charles DeCarli, John C. DeToledo, Dennis W. Dickson, Nic Dobbins, Ranjan Duara, Nilüfer Ertekin‐Taner, Denis A. Evans, Kelley Faber, Thomas Fairchild, M. Daniele Fallin, Kenneth B. Fallon, David W. Fardo, Martin R. Farlow, John J. Farrell, Lindsay A. Farrer and 273 more - JAMA Neurology 2023 cited by 56
- Common genetic variants on 5p14.1 associate with autism spectrum disorders
Authors: Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bućan, Joseph Glessner, Brett S. Abrahams, Daria Salyakina, Marcin Imieliński, Jonathan P. Bradfield, Patrick Sleiman, Cecilia E. Kim, Cuiping Hou, Edward C. Frackelton, Rosetta Chiavacci, Nagahide Takahashi, Takeshi Sakurai, Eric Rappaport, Clara Lajonchere, Jeffrey Munson, Annette Estes, Olena Korvatska, Joseph Piven, Lisa I. Sonnenblick, Ana I. Alvarez Retuerto, Edward I. Herman, Hongmei Dong, Ted Hutman, Marian Sigman, Sally Ozonoff, Ami Klin, Thomas Owley, John A. Sweeney, Camille W. Brune, Rita M. Cantor, Raphael Bernier, John R. Gilbert, Michael L. Cuccaro, William M. McMahon, Judith Miller, Matthew W. State, Thomas H. Wassink, Hilary Coon, Susan E. Levy, Robert T. Schultz, John I. Nürnberger, Jonathan L. Haines, James S. Sutcliffe, Edwin H. Cook, Nancy J. Minshew, Joseph D. Buxbaum, Géraldine Dawson, Struan F.A. Grant, Daniel H. Geschwind, Margaret A. Pericak‐Vance, Gerard D. Schellenberg, Håkon Håkonarson - Nature 2009 cited by 975
- ABCA7 frameshift deletion associated with Alzheimer disease in African Americans
Authors: Holly N. Cukier, Brian W. Kunkle, Badri N. Vardarajan, Sophie Rolati, Kara L. Hamilton‐Nelson, Martin Kohli, Patrice L. Whitehead, Beth A. Dombroski, Derek Van Booven, Rosalyn Lang, Derek M. Dykxhoorn, Lindsay A. Farrer, Michael L. Cuccaro, Jeffery M. Vance, John R. Gilbert, Gary W. Beecham, Eden R. Martin, Regina M. Carney, Richard Mayeux, Gerard D. Schellenberg, Goldie S. Byrd, Jonathan L. Haines, Margaret A. Pericak‐Vance, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig Atwood, Clinton T. Baldwin, M. Michael Barmada, Lisa L. Barnes, Sandra Barral, Thomas G. Beach, James T. Becker, Gary W. Beecham, Duane Beekly, David A. Bennett, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, Adam Boxer, James R. Burke, Jeffrey M. Burns, Joseph D. Buxbaum, Goldie S. Byrd, Guiqing Cai, Nigel J. Cairns, Laura B. Cantwell, Chuanhai Cao, Cynthia M. Carlsson, Regina M. Carney, Minerva M. Carrasquillo, Steven L. Carroll, Helena C. Chui, David G. Clark, David H. Cribbs, Elizabeth Crocco, Carlos Cruchaga, Philip L. De Jager, Charles DeCarli, F. Yesim Demirci, Malcolm Dick, Dennis W. Dickson, Ranjan Duara, Nilüfer Ertekin‐Taner, Denis A. Evans, Kelley Faber, M. Daniele Fallin, Kenneth B. Fallon, David W. Fardo, Martin R. Farlow, Lindsay A. Farrer, Steven H. Ferris, Tatiana Foroud, Matthew P. Frosch, Douglas Galasko, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Rodney C.P. Go, Alison Goate, Neill R. Graff‐Radford, Robert C. Green, Patrick Griffith, John H. Growdon, Jonathan L. Haines, Håkon Håkonarson, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Vahram Haroutunian, Lindy E. Harrell, Lawrence S. Honig, Ryan Huebinger, Christine M. Hulette, Bradley T. Hyman, Gregory A. Jicha, Lee‐Way Jin and 97 more - Neurology Genetics 2016 cited by 107
- Reconstructing the Population Genetic History of the Caribbean
Authors: Andrés Moreno‐Estrada, Simon Gravel, Fouad Zakharia, Jacob L. McCauley, Jake Byrnes, Christopher R. Gignoux, Patricia A. Ortiz-Tello, Ricardo Martínez, Dale J. Hedges, Richard Morris, Celeste Eng, Karla Sandoval, Suehelay Acevedo‐Acevedo, Paul J. Norman, Z. Layrisse, Peter Parham, Juan Carlos Martínez‐Cruzado, Esteban G. Burchard, Michael L. Cuccaro, Eden R. Martin, Carlos D. Bustamante - PLoS Genetics 2013 cited by 366
- Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Authors: Péter Szatmári, Ping G. Tepper, Ann Thompson, Jennifer Skaug, Andrew D. Paterson, Lars Feuk, Qian Cheng, Christian R. Marshall, Christian R Marshall, Stephen W. Scherer, Lonnie Zwaigenbaum, Jessica Brian, Lili Senman, Wendy Roberts, John B. Vincent, Susan E. Bryson, Marshall B. Jones, Veronica J. Vieland, La Vonne Mangin, Christopher W. Bartlett, Alberto M. Segre, Rhinda Goedken, Michael L. Cuccaro, Margaret A. Pericak‐Vance, John R. Gilbert, Harry H. Wright, Ruth K. Abramson, Catalina Betancur, Marion Leboyer, Thomas Bourgeron, Christopher Gillberg, Marion Leboyer, Eric Hollander, Jeremy M. Silverman, Kenneth L. Davis, Joseph D. Buxbaum, Linda Lotspeich, Joachim Hallmayer, James S. Sutcliffe, James S. Sutcliffe, Jonathan L. Haines, Susan E. Folstein, Joseph Piven, Val C. Sheffield, Kacie J. Meyer, Thomas H. Wassink, Daniel H. Geschwind, Maja Bućan, W. Ted Brown, Rita M. Cantor, Stan F. Nelson, John N. Constantino, T. Conrad Gilliam, Martha R. Herbert, Janet Miller, Clara Lajonchere, David H. Ledbetter, Christa Lese‐Martin, Carol A Samango-Sprouse, Sarah Spence, Fred R. Volkmar, Matthew W. State, Rudolph E. Tanzi, Hilary Coon, William M. McMahon, Jeff Munson, Géraldine Dawson, Géraldine Dawson, Annette Estes, Lambertus Klei, Nancy J. Minshew, Bernie Devlin, Pamela Flodman, Moyra Smith, M. Anne Spence, Chang-En Yu, Gerard D. Schellenberg, Elena Korvatska, Bernadette Rogé, Gerard D. Schellenberg, Elena Korvatska, Patricia M. Rodier, Chris Stodgell, Gerard D. Schellenberg, Ellen M. Wijsman, Ellen M. Wijsman, Kerstin Wittemeyer, Bernadette Rogé, Carine Mantoulan, Bärbel Felder, Sabine M. Klauck, Annemarie Poustka, Claudia Schuster, Gabi Schmötzer, Sven Bölte, Fritz Poustka, Sabine Feineis-Matthews, Evelyn Herbrecht, Κaterina Papanikolaou, John Tsiantis and 38 more - Nature Genetics 2007 cited by 1,416
- Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders
Authors: Holly N. Cukier, Nicole Dueker, Susan H. Slifer, Joycelyn M. Lee, Patrice L. Whitehead, Eminisha Lalanne, Natalia Leyva, Ioanna Konidari, Ryan C Gentry, William Hulme, Derek Van Booven, Vera Mayo, Natalia K. Hofmann, Michael A. Schmidt, Eden R. Martin, Jonathan L. Haines, Michael L. Cuccaro, John R. Gilbert, Margaret A. Pericak‐Vance - Molecular Autism 2014 cited by 329
- Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
Authors: Simon G. Gregory, Jessica J. Connelly, Aaron J. Towers, Jessica Johnson, Dhani Biscocho, Christina A. Markunas, Carla Lintas, Ruth K. Abramson, Harry H. Wright, Peter Ellis, Cordelia F. Langford, Gordon Worley, G. Robert DeLong, Susan K. Murphy, Michael L. Cuccaro, Antonello Persico, Margaret A. Pericak‐Vance - BMC Medicine 2009 cited by 576
- Manifestations of Alzheimer’s disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90
Authors: Laura Heath, John C. Earls, Andrew T. Magis, Sergey A. Kornilov, Jennifer C. Lovejoy, Cory C. Funk, Noa Rappaport, Benjamin A. Logsdon, Lara M. Mangravite, Brian W. Kunkle, Eden R. Martin, Adam C. Naj, Nilüfer Ertekin‐Taner, Todd E. Golde, Leroy Hood, Nathan D. Price, Erin L. Abner, Perrie M. Adams, Marilyn S. Albert, Roger L. Albin, Mariet Allen, Alexandre Amlie‐Wolf, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig Atwood, Clinton T. Baldwin, Robert C. Barber, Lisa L. Barnes, Sandra Barral, Thomas G. Beach, James T. Becker, Gary W. Beecham, Duane Beekly, David Bennett, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, James D. Bowen, Adam Boxer, James R. Burke, Jeffrey M. Burns, William S. Bush, Mariusz Butkiewicz, Joseph D. Buxbaum, Nigel J. Cairns, Laura B. Cantwell, Chuanhai Cao, Chris Carlson, Cynthia M. Carlsson, Regina M. Carney, Helena C. Chui, Paul K. Crane, David H. Cribbs, Elizabeth Crocco, Michael L. Cuccaro, Philip L. De Jager, Charles DeCarli, Malcolm Dick, Dennis W. Dickson, Beth A. Dombroski, Rachelle S. Doody, Ranjan Duara, Nilüfer Ertekin‐Taner, Denis A. Evans, Kelley M. Faber, Thomas Fairchild, Kenneth B. Fallon, David W. Fardo, Martin R. Farlow, Lindsay A. Farrer, Steven H. Ferris, Tatiana Foroud, Matthew P. Frosch, Douglas Galasko, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Alison Goate, Robert C. Green, John H. Growdon, Jonathan L. Haines, Håkon Håkonarson, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Lindy E. Harrell, Lawrence S. Honig, Ryan M. Huebinger, Matthew J. Huentelman, Christine M. Hulette, Bradley T. Hyman, Gail P. Jarvik, Lee‐Way Jin, Gyungah Jun, M. Ilyas Kamboh, Anna Karydas, Mindy J. Katz, Jeffrey A. Kaye and 102 more - Scientific Reports 2022 cited by 28
- Extended genome‐wide association study employing the African genome resources panel identifies novel susceptibility loci for Alzheimer's disease in individuals of African ancestry
Authors: Nicholas R. Ray, Brian W. Kunkle, Kara L. Hamilton‐Nelson, Jiji T. Kurup, Farid Rajabli, Min Qiao, Badri N. Vardarajan, Mehmet İlyas Coşacak, Çağhan Kızıl, Melissa Jean‐Francois, Michael L. Cuccaro, Dolly Reyes‐Dumeyer, Laura Cantwell, Amanda Kuzma, Jeffery M. Vance, Sujuan Gao, Hugh C. Hendrie, Olusegun Baiyewu, Adesola Ogunniyi, Rufus Akinyemi, Wan‐Ping Lee, Eden R. Martin, Li‐San Wang, Gary W. Beecham, William S. Bush, Wanying Xu, Fulai Jin, Liyong Wang, Lindsay A. Farrer, Jonathan L. Haines, Goldie S. Byrd, Gerard D. Schellenberg, Richard Mayeux, Margaret A. Pericak‐Vance, Christiane Reitz - Alzheimer s & Dementia 2024 cited by 24
- Repetitive behaviors in autism: relationships with associated clinical features
Authors: Robin L. Gabriels, Michael L. Cuccaro, Dina E. Hill, Bonnie Jean Ivers, Edward Goldson - Research in Developmental Disabilities 2004 cited by 333
- A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism
Authors: John P. Hussman, Ren-Hua Chung, Anthony J. Griswold, James Jaworski, Daria Salyakina, Deqiong Ma, Ioanna Konidari, Patrice L. Whitehead, Jeffery M. Vance, Eden R. Martin, Michael L. Cuccaro, John R. Gilbert, Jonathan L. Haines, Margaret A. Pericak‐Vance - Molecular Autism 2011 cited by 234
- Convergent Pathways in Idiopathic Autism Revealed by Time Course Transcriptomic Analysis of Patient-Derived Neurons
Authors: Brooke A. DeRosa, Jimmy El Hokayem, Elena Artimovich, Catherine Garcia‐Serje, André W. Phillips, Derek Van Booven, Jonathan E. Nestor, Lily Wang, Michael L. Cuccaro, Jeffery M. Vance, Margaret A. Pericak‐Vance, Holly N. Cukier, Michael W. Nestor, Derek M. Dykxhoorn - Scientific Reports 2018 cited by 100
- Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism
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