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Flora Tassone

Active 1999–2025

153
Papers
22,169
Citations
86
h-index
140
i10-index

Citations

Citations per year for Flora Tassone1933: 1 citations1999: 5 citations2000: 24 citations2001: 33 citations2002: 43 citations2003: 71 citations2004: 140 citations2005: 111 citations2006: 154 citations2007: 211 citations2008: 284 citations2009: 218 citations2010: 293 citations2011: 368 citations2012: 257 citations2013: 290 citations2014: 393 citations2015: 148 citations2016: 154 citations2017: 181 citations2018: 147 citations2019: 540 citations2020: 645 citations2021: 556 citations2022: 458 citations2023: 343 citations2024: 527 citations2025: 189 citations2026: 4 citations1934–1998: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 1,806 citing papers, 36.8% of this breakdownUnited Kingdom: 304 citing papers, 6.2% of this breakdownItaly: 262 citing papers, 5.3% of this breakdownCanada: 223 citing papers, 4.5% of this breakdownChina: 223 citing papers, 4.5% of this breakdownFrance: 174 citing papers, 3.6% of this breakdownGermany: 160 citing papers, 3.3% of this breakdownNetherlands: 155 citing papers, 3.2% of this breakdownAustralia: 152 citing papers, 3.1% of this breakdownJapan: 118 citing papers, 2.4% of this breakdownSpain: 109 citing papers, 2.2% of this breakdownBelgium: 83 citing papers, 1.7% of this breakdown
0%36.8%Other 23.2%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology58.5%
  • Neuroscience24.6%
  • Medicine13.1%
  • Psychology1.4%
  • Agricultural and Biological Sciences0.7%
  • Environmental Science0.5%
  • Other1.2%

Topics

  • Genetics and Neurodevelopmental Disorders17%
  • Autism Spectrum Disorder Research12.1%
  • Genetic Neurodegenerative Diseases4%
  • Congenital heart defects research3.2%
  • RNA modifications and cancer2.9%
  • RNA Research and Splicing2.7%
  • Other58.1%

Coauthors

All papers

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  1. 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, 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

  2. Fragile X syndrome

    Authors: Randi J. Hagerman, Elizabeth Berry‐Kravis, Heather C. Hazlett, Donald B. Bailey, Hervé Moine, R. Frank Kooy, Flora Tassone, Ilse Gantois, Nahum Sonenberg, Jean‐Louis Mandel, Paul J. Hagerman - Nature Reviews Disease Primers 2017 cited by 779

  3. A randomized, controlled trial of ZYN002 cannabidiol transdermal gel in children and adolescents with fragile X syndrome (CONNECT-FX)

    Authors: Elizabeth Berry‐Kravis, Randi J. Hagerman, Dejan B. Budimirovic, Craig A. Erickson, Helen Heussler, Nicole Tartaglia, Jonathan Cohen, Flora Tassone, Thomas W Dobbins, Elizabeth Merikle, Terri Sebree, Nancy Tich, Joseph Palumbo, Stephen O’Quinn - Journal of Neurodevelopmental Disorders 2022 cited by 66

  4. Disease-Associated Short Tandem Repeats Co-localize with Chromatin Domain Boundaries

    Authors: James Sun, Linda Zhou, Daniel J. Emerson, Sai Aung Phyo, Katelyn R. Titus, Wanfeng Gong, Thomas G. Gilgenast, Jonathan A. Beagan, Beverly L. Davidson, Flora Tassone, Jennifer E. Phillips‐Cremins - Cell 2018 cited by 295

  5. Translation of Expanded CGG Repeats into FMRpolyG Is Pathogenic and May Contribute to Fragile X Tremor Ataxia Syndrome

    Authors: Chantal Sellier, Ronald A.M. Buijsen, Fang He, Sam Natla, Laura Jung, Philippe Tropel, Angéline Gaucherot, Hugues Jacobs, Hamid Méziane, Alexandre Vincent, Marie‐France Champy, Tania Sorg, Guillaume Pavlovic, Marie Wattenhofer‐Donzé, Marie‐Christine Birling, Mustapha Oulad‐Abdelghani, Pascal Eberling, Frank Ruffenach, Mathilde Joint, Mathieu Anheim, Verónica Martínez‐Cerdeño, Flora Tassone, Rob Willemsen, Renate K. Hukema, Stéphane Viville, Cécile Martinat, Peter K. Todd, Nicolas Charlet‐Berguerand - Neuron 2017 cited by 244

  6. Mitochondrial Dysfunction in Autism

    Authors: Cecilia Giulivi, Yi Fan Zhang, Alicja Omanska-Klusek, Catherine Ross‐Inta, Sarah Wong, Irva Hertz‐Picciotto, Flora Tassone, Isaac N. Pessah - JAMA 2010 cited by 473

  7. Maternal periconceptional folic acid intake and risk of autism spectrum disorders and developmental delay in the CHARGE (CHildhood Autism Risks from Genetics and Environment) case-control study

    Authors: Rebecca J. Schmidt, Daniel J. Tancredi, Sally Ozonoff, Robin Hansen, Jaana Hartiala, Hooman Allayee, Linda C. Schmidt, Flora Tassone, Irva Hertz‐Picciotto - American Journal of Clinical Nutrition 2012 cited by 403

  8. Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation

    Authors: Flora Tassone, Dragana Protić, Emily G. Allen, Alison D. Archibald, Anna Baud, Ted W. Brown, Dejan B. Budimirovic, Jonathan Cohen, Brett D. Dufour, Rachel Eiges, Nicola Elvassore, Lidia V. Gabis, Samantha J. Grudzien, Deborah A. Hall, David Hessl, Abigail L. Hogan, Jessica Ezzell Hunter, Peng Jin, Poonnada Jiraanont, Jessica Klusek, R. Frank Kooy, Claudine M. Kraan, Cecilia Laterza, Andrea Lee, Karen Lipworth, Molly Losh, Danuta Z. Loesch, Reymundo Lozano, Marsha R. Mailick, Apostolos Manolopoulos, Verónica Martínez‐Cerdeño, Yingratana McLennan, Robert M. Miller, Federica Alice Maria Montanaro, Matthew W. Mosconi, Sarah Nelson Potter, Melissa Raspa, Susan M. Rivera, Katharine E. Shelly, Peter K. Todd, Katarzyna Tutak, Jun Yi Wang, Anne Wheeler, Tri Indah Winarni, Marwa Zafarullah, Randi J. Hagerman - Cells 2023 cited by 66

  9. Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics

    Authors: Claudia Bagni, Flora Tassone, Giovanni Neri, Randi J. Hagerman - Journal of Clinical Investigation 2012 cited by 326

  10. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X

    Authors: Randi J. Hagerman, Maureen A. Leehey, W L Heinrichs, Flora Tassone, Rebecca L. Wilson, John D Hills, Jim Grigsby, Brian F. Gage, Paul J. Hagerman - Neurology 2001 cited by 972

  11. FMR1 CGG allele size and prevalence ascertained through newborn screening in the United States

    Authors: Flora Tassone, Ka Pou Iong, Tzuhan Tong, Joyce Lo, Louise W. Gane, Elizabeth Berry‐Kravis, Danh V. Nguyen, Lisa Y Mu, Jennifer Laffin, Donald B. Bailey, Randi J. Hagerman - Genome Medicine 2012 cited by 321

  12. Prenatal Vitamins, One-carbon Metabolism Gene Variants, and Risk for Autism

    Authors: Rebecca J. Schmidt, Robin Hansen, Jaana Hartiala, Hooman Allayee, Linda C. Schmidt, Daniel J. Tancredi, Flora Tassone, Irva Hertz‐Picciotto - Epidemiology 2011 cited by 313

  13. Metformin treatment in young children with fragile X syndrome

    Authors: Hazel Maridith Barlahan Biag, Laura A. Potter, Victoria Wilkins, Sumra Afzal, Alexis Rosvall, María Jimena Salcedo‐Arellano, Akash Rajaratnam, Ramiro Manzano-Núñez, Andrea Schneider, Flora Tassone, Susan M. Rivera, Randi J. Hagerman - Molecular Genetics & Genomic Medicine 2019 cited by 66

  14. Metformin as targeted treatment in fragile X syndrome

    Authors: Angel Belle C. Dy, Flora Tassone, Mona Kamal Eldeeb, María Jimena Salcedo‐Arellano, Nicole Tartaglia, Randi J. Hagerman - Clinical Genetics 2017 cited by 119

  15. Elevated Levels of FMR1 mRNA in Carrier Males: A New Mechanism of Involvement in the Fragile-X Syndrome

    Authors: Flora Tassone, Randi J. Hagerman, Annette K. Taylor, Louise W. Gane, Tony E. Godfrey, Paul J. Hagerman - The American Journal of Human Genetics 2000 cited by 771

  16. Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report

    Authors: Lucy Miller, Daniel N. McIntosh, J. McGrath, Vivian Shyu, Megan Lampe, Annette K. Taylor, Flora Tassone, Kari Neitzel, Tracy Stackhouse, Randi J. Hagerman - American Journal of Medical Genetics 1999 cited by 396

  17. Increased number of sex chromosomes affects height in a nonlinear fashion: A study of 305 patients with sex chromosome aneuploidy

    Authors: Anne Marie Ottesen, Lise Aksglæde, Inger Garn, Nicole Tartaglia, Flora Tassone, Claus Højbjerg Gravholt, Anders Bojesen, Kaspar Sørensen, Niels Jørgensen, Ewa Rajpert‐De Meyts, Tommy Gerdes, Anne‐Marie Lind, Susanne Kjærgaard, Anders Juul - American Journal of Medical Genetics Part A 2010 cited by 224

  18. Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndrome

    Authors: Charles A. Hoeffer, E. Sanchez, Randi J. Hagerman, Yi Mu, Danh V. Nguyen, Helen Wong, Ashley Whelan, R. Suzanne Zukin, Eric Klann, Flora Tassone - Genes Brain & Behavior 2012 cited by 201

  19. Episignatures Stratifying Helsmoortel-Van Der Aa Syndrome Show Modest Correlation with Phenotype

    Authors: Michael S. Breen, Paras Garg, Lara Tang, Danielle Mendonca, Tess Levy, Mafalda Barbosa, Anne B. Arnett, Evangeline C. Kurtz‐Nelson, Emanuele Agolini, Agatino Battaglia, Andreas G. Chiocchetti, Christine M. Freitag, Alicia García-Alcón, Paola Grammatico, Irva Hertz‐Picciotto, Yunin Ludena‐Rodriguez, Carmen Moreno, Antonio Novelli, Mara Parellada, Giulia Pascolini, Flora Tassone, Dorothy E. Grice, Daniele Di Marino, Raphael Bernier, A lexander Kolevzon, Andrew J. Sharp, Joseph D. Buxbaum, Paige M. Siper, Silvia De Rubeis - The American Journal of Human Genetics 2020 cited by 54

  20. Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates

    Authors: Sébastien Jacquemont, Randi J. Hagerman, Maureen A. Leehey, Jim Grigsby, Lin Zhang, James A. Brunberg, Claudia Greco, Vincent des Portes, Tristan Jardini, Richard A. Levine, Elizabeth Berry‐Kravis, W. Ted Brown, S. Schaeffer, John T. Kissel, Flora Tassone, Paul J. Hagerman - The American Journal of Human Genetics 2003 cited by 765

  21. Sam68 sequestration and partial loss of function are associated with splicing alterations in FXTAS patients

    Authors: Chantal Sellier, Frédérique Rau, Yilei Liu, Flora Tassone, Renate K. Hukema, Renata Gattoni, Anne Schneider, Stéphane Richard, Rob Willemsen, David J. Elliott, Paul J. Hagerman, Nicolas Charlet‐Berguerand - The EMBO Journal 2010 cited by 365

  22. A Randomized Double-Blind, Placebo-Controlled Trial of Minocycline in Children and Adolescents with Fragile X Syndrome

    Authors: Mary Jacena Leigh, Danh V. Nguyen, Yi Mu, Tri Indah Winarni, Andrea Schneider, Tasleem Chechi, Jonathan Polussa, Paul Doucet, Flora Tassone, Susan M. Rivera, David Hessl, Randi J. Hagerman - Journal of Developmental & Behavioral Pediatrics 2013 cited by 298

  23. A Novel FMR1 PCR Method for the Routine Detection of Low Abundance Expanded Alleles and Full Mutations in Fragile X Syndrome

    Authors: Stela Filipovic-Sadic, Sachin Sah, Liangjing Chen, Julie Krosting, Edward A. Sekinger, Wenting Zhang, Paul J. Hagerman, Timothy T. Stenzel, Andrew G. Hadd, Gary J. Latham, Flora Tassone - Clinical Chemistry 2010 cited by 278

  24. Sequestration of DROSHA and DGCR8 by Expanded CGG RNA Repeats Alters MicroRNA Processing in Fragile X-Associated Tremor/Ataxia Syndrome

    Authors: Chantal Sellier, Fernande Freyermuth, Ricardos Tabet, Tuan Anh Tran, Fang He, Frank Ruffenach, Violaine Alunni, Hervé Moine, Christelle Thibault-Carpentier, Adeline Page, Flora Tassone, Rob Willemsen, Matthew D. Disney, P. J. Hagerman, Peter K. Todd, Nicolas Charlet‐Berguerand - Cell Reports 2013 cited by 261