Michael L. Cuccaro

Active 1995–2025

83
Papers
18,123
Citations
52
h-index
72
i10-index

Citations

Citations per year for Michael L. Cuccaro1967: 1 citations1995: 4 citations1996: 1 citations1998: 5 citations1999: 13 citations2000: 22 citations2001: 54 citations2002: 45 citations2003: 67 citations2004: 102 citations2005: 115 citations2006: 121 citations2007: 108 citations2008: 191 citations2009: 174 citations2010: 204 citations2011: 174 citations2012: 195 citations2013: 199 citations2014: 166 citations2015: 178 citations2016: 159 citations2017: 139 citations2018: 97 citations2019: 340 citations2020: 469 citations2021: 505 citations2022: 497 citations2023: 556 citations2024: 898 citations2025: 502 citations2026: 14 citations1968–1994: no citations, so these years are not shown1997: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,182 citing papers, 32.6% of this breakdownUnited Kingdom: 781 citing papers, 8% of this breakdownCanada: 508 citing papers, 5.2% of this breakdownChina: 497 citing papers, 5.1% of this breakdownGermany: 453 citing papers, 4.6% of this breakdownItaly: 335 citing papers, 3.4% of this breakdownFrance: 313 citing papers, 3.2% of this breakdownNetherlands: 306 citing papers, 3.1% of this breakdownAustralia: 295 citing papers, 3% of this breakdownSpain: 230 citing papers, 2.4% of this breakdownSweden: 207 citing papers, 2.1% of this breakdownJapan: 190 citing papers, 2% of this breakdown
0%32.6%Other 25.3%

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

All papers

Open in search
  1. New insights into the genetic etiology of Alzheimer’s disease and related dementias

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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, Ángel 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

  2. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ángel 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

  3. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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, Ángel 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

  4. APOE Genotype and Alzheimer Disease Risk Across Age, Sex, and Population Ancestry

    Authors: , , , , , , - JAMA Neurology 2023 cited by 280

  5. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  6. Sex differences in the genetic architecture of cognitive resilience to Alzheimer’s disease

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  7. Ancestral origin of ApoE ε4 Alzheimer disease risk in Puerto Rican and African American populations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - PLoS Genetics 2018 cited by 202

  8. A locus at 19q13.31 significantly reduces the ApoE ε4 risk for Alzheimer’s Disease in African Ancestry

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - PLoS Genetics 2022 cited by 63

  9. Cognitive domain harmonization and cocalibration in studies of older adults.

    Authors: , , , , , , , , , , , , , , , , , , , , - Neuropsychology 2022 cited by 99

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  11. Common genetic variants on 5p14.1 associate with autism spectrum disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  12. ABCA7 frameshift deletion associated with Alzheimer disease in African Americans

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  13. Reconstructing the Population Genetic History of the Caribbean

    Authors: , , , , , , , , , , , , , , , , , , , , - PLoS Genetics 2013 cited by 366

  14. Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  15. Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders

    Authors: , , , , , , , , , , , , , , , , , , - Molecular Autism 2014 cited by 329

  16. Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

    Authors: , , , , , , , , , , , , , , , , - BMC Medicine 2009 cited by 576

  17. Manifestations of Alzheimer’s disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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

  18. 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: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Goldie S. Byrd, Gerard D. Schellenberg, Richard Mayeux, Margaret A. Pericak‐Vance, Christiane Reitz - Alzheimer s & Dementia 2024 cited by 24

  19. Repetitive behaviors in autism: relationships with associated clinical features

    Authors: , , , , - Research in Developmental Disabilities 2004 cited by 333

  20. A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

    Authors: , , , , , , , , , , , , , - Molecular Autism 2011 cited by 234

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

    Authors: , , , , , , , , , , , , , - Scientific Reports 2018 cited by 100

  22. Identification of Significant Association and Gene-Gene Interaction of GABA Receptor Subunit Genes in Autism

    Authors: , , , , , , , , , , , , , - The American Journal of Human Genetics 2005 cited by 359

  23. Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joseph Biederman, Elisabeth B. Binder, Donald W. Black, Douglas Blackwood, Cinnamon S. Bloss, Michael Boehnke, Dorret I. Boomsma, Gerome Breen, René Breuer, Richard Bruggeman, Nancy G. Buccola, Jan K. Buitelaar, William E. Bunney, Joseph D. Buxbaum, William Byerley, Sian Caesar, Wiepke Cahn, Rita M. Cantor, Miguel Casas, Aravinda Chakravarti, Kimberly Chambert, Khalid Choudhury, Sven Cichon, C. Robert Cloninger, David Collier, Edwin H. Cook, Hilary Coon, Bru Cormand, Paul Cormican, Aiden Corvin, William Coryell, Nicholas Craddock, David W. Craig, Ian Craig, Jennifer Crosbie, Michael L. Cuccaro, David Curtis, Darina Czamara, Mark J. Daly, Susmita Datta, Géraldine Dawson, Richard Day, Eco J. C. de Geus, Franziska Degenhardt, Bernie Devlin, Srdjan Djurovic, Gary Donohoe, Alysa E. Doyle, Jubao Duan, Frank Dudbridge, Eftichia Duketis, Richard P. Ebstein, Howard J. Edenberg, Josephine Elia, Sean Ennis, Bruno Étain, Ayman Fanous, Stephen V. Faraone, Anne Farmer, I. Nicol Ferrier, Matthew Flickinger, Éric Fombonne, Tatiana Foroud, Josef Frank, Barbara Franke, Christine Fraser, Robert Freedman, Nelson B. Freimer, Christine M. Freitag, Marion Friedl and 280 more - The American Journal of Human Genetics 2015 cited by 270

  24. Identification of MeCP2 mutations in a series of females with autistic disorder

    Authors: , , , , , , , - Pediatric Neurology 2003 cited by 230