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F. Cerrato · SciRah

Researcher profile · Semantic Scholar

F. Cerrato

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F. Cerrato — researcher profile on SciRah

h-index: 31
Works: 50
Citations: 9,547

Most-cited papers

Identification of common genetic risk variants for autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +272 more
2019Nature Genetics2,146 citations Open access
Semantic Scholar
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +186 more
2019Cell2,103 citations Open access
Semantic Scholar
Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder
D. Demontis, R. Walters, Joanna Martin, M. Mattheisen +217 more
2018Nature Genetics1,852 citations Open access
Semantic Scholar
Kiss1-/- mice exhibit more variable hypogonadism than Gpr54-/- mice.
R. Lapatto, J. C. Pallais, Dongsheng Zhang, Yee-Ming Chan +5 more
2007Endocrinology510 citations
Semantic Scholar
Phylogenetic analysis of SARS-CoV-2 in Boston highlights the impact of superspreading events
J. Lemieux, K. Siddle, B. Shaw, Christine Loreth +49 more
2020Science277 citations Open access
Semantic Scholar
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
Y. Feng, D. Howrigan, L. Abbott, K. Tashman +236 more
2019bioRxiv268 citations Open access
Semantic Scholar
Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variants
N. Welch, Meilin Zhu, C. Hua, J. Weller +46 more
2022Nature Medicine259 citations Open access
Semantic Scholar
Discovery of the first genome-wide significant risk loci for ADHD
D. Demontis, R. Walters, Joanna Martin, M. Mattheisen +67 more
2017bioRxiv231 citations Open access
Semantic Scholar
GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture
R. Stevelink, C. Campbell, Si-Wei Chen, B. Abou-Khalil +315 more
2023Nature Genetics198 citations Open access
Semantic Scholar
GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism
Yee-Ming Chan, Adelaide de Guillebon, M. Lang-Muritano, L. Plummer +9 more
2009Proceedings of the National Academy of Sciences of the United States of America196 citations Open access
Semantic Scholar
Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations
D. Howrigan, S. Rose, K. Samocha, M. Fromer +20 more
2020Nature Neuroscience157 citations Open access
Semantic Scholar
Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: Variant reclassification and surgical decisions
Mitzi L. Murray, F. Cerrato, R. Bennett, G. Jarvik
2011Genetics in Medicine141 citations Open access
Semantic Scholar
Common risk variants identified in autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +71 more
2017bioRxiv105 citations Open access
Semantic Scholar
Mutations in KCTD1 cause scalp-ear-nipple syndrome.
Alexander G. Marneros, A. Beck, Emily H. Turner, Margaret J. McMillin +20 more
2013American Journal of Human Genetics83 citations Open access
Semantic Scholar
Diagnosis and Management of Fibroadenomas in the Adolescent Breast
F. Cerrato, B. Labow
2013Seminars in Plastic Surgery83 citations Open access
Semantic Scholar
Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism.
F. Cerrato, Jenna K Shagoury, M. Králíčková, A. Dwyer +10 more
2006European Journal of Endocrinology78 citations Open access
Semantic Scholar
Psychosocial Impact of Adolescent Gynecomastia: A Prospective Case-Control Study
Laura C. Nuzzi, F. Cerrato, Cameron R. Erikson, M. Webb +5 more
2013Plastic and Reconstructive Surgery69 citations
Semantic Scholar
GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1.
Yee-Ming Chan, Sarabeth Broder-Fingert, Sophia Paraschos, R. Lapatto +24 more
2011Journal of Clinical Endocrinology and Metabolism66 citations Open access
Semantic Scholar
The Impact of Macromastia on Adolescents: A Cross-Sectional Study
F. Cerrato, M. Webb, Heather Rosen, Laura C. Nuzzi +4 more
2012Pediatrics60 citations Open access
Semantic Scholar
Presentation and treatment of macrodactyly in children.
F. Cerrato, K. Eberlin, P. Waters, J. Upton +2 more
2013Journal of Hand Surgery-American Volume59 citations
Semantic Scholar
The Effect of Reduction Mammaplasty on Quality of Life in Adolescents With Macromastia
Laura C. Nuzzi, Joseph M. Firriolo, Carolyn M. Pike, F. Cerrato +4 more
2017Pediatrics54 citations Open access
Semantic Scholar
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
Joshua E. Motelow, G. Povysil, R. Dhindsa, Kate E. Stanley +251 more
2021American Journal of Human Genetics53 citations Open access
Semantic Scholar
Phylogenetic analysis of SARS-CoV-2 in the Boston area highlights the role of recurrent importation and superspreading events.
J. Lemieux, K. Siddle, B. Shaw, Christine Loreth +49 more
2020medRxiv52 citations Open access
Semantic Scholar
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Si-Wei Chen, B. Abou-Khalil, Z. Afawi, Q. Z. Ali +332 more
2024Nature Neuroscience50 citations Open access
Semantic Scholar
Psychological Impact of Breast Asymmetry on Adolescents: A Prospective Cohort Study
Laura C. Nuzzi, F. Cerrato, M. Webb, Heather R. Faulkner +4 more
2014Plastic and Reconstructive Surgery49 citations
Semantic Scholar
Genetic variation in LPAL2, LPA, and PLG predicts plasma lipoprotein(a) level and carotid artery disease risk
James Ronald, R. Rajagopalan, F. Cerrato, A. Nord +5 more
2010Stroke47 citations Open access
Semantic Scholar
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes
Si-Wei Chen, B. Abou-Khalil, Z. Afawi, Q. Z. Ali +332 more
2023medRxiv44 citations Open access
Semantic Scholar
The Effect of Obesity on Early Outcomes in Adolescents Undergoing Reduction Mammaplasty
M. Webb, F. Cerrato, Heather Rosen, Amy D. DiVasta +2 more
2012Annals of Plastic Surgery39 citations
Semantic Scholar
Outcomes in Pediatric Atypical Spitz Tumors Treated Without Sentinel Lymph Node Biopsy
F. Cerrato, Joseph S. Wallins, M. Webb, Erika R. McCarty +2 more
2012Pediatric dermatology37 citations
Semantic Scholar
Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity
V. Rajagopal, A. Ganna, J. Coleman, A. Allegrini +49 more
2023Scientific Reports32 citations Open access
Semantic Scholar
The Effect of Surgical Treatment for Gynecomastia on Quality of Life in Adolescents.
Laura C. Nuzzi, Joseph M. Firriolo, Carolyn M. Pike, F. Cerrato +2 more
2018Journal of Adolescent Health31 citations
Semantic Scholar
Genetic risk for schizophrenia and autism, social impairment and developmental pathways to psychosis
E. Velthorst, S. Froudist-Walsh, E. Stahl, D. Ruderfer +51 more
2018Translational Psychiatry25 citations Open access
Semantic Scholar
Incidence of Fanconi anemia in children with congenital thumb anomalies referred for diepoxybutane testing.
M. Webb, Heather Rosen, Amir H. Taghinia, Erika R. McCarty +3 more
2011Journal of Hand Surgery-American Volume22 citations
Semantic Scholar
Human genetics of GPR54
F. Cerrato, S. Seminara
2007Reviews in Endocrine & Metabolic Disorders19 citations
Semantic Scholar
Intermediate and Long‐term Outcomes of Giant Fibroadenoma Excision in Adolescent and Young Adult Patients
F. Cerrato, S. Pruthi, J. Boughey, P. S. Simmons +4 more
2015The Breast Journal14 citations Open access
Semantic Scholar
Body fluid biomarkers and psychosis risk in The Accelerating Medicines Partnership® Schizophrenia Program: design considerations
D. Perkins, Clark D. Jeffries, S. Clark, R. Upthegrove +35 more
2025Schizophrenia13 citations Open access
Semantic Scholar
The Effect of Surgical Treatment on the Quality of Life of Young Women with Breast Asymmetry: A Longitudinal, Cohort Study
Laura C. Nuzzi, Joseph M. Firriolo, Carolyn M. Pike, F. Cerrato +2 more
2020Plastic and Reconstructive Surgery9 citations
Semantic Scholar
Schizophrenia risk conferred by protein-coding de novo mutations
D. Howrigan, S. Rose, K. Samocha, M. Fromer +20 more
20187 citations Open access
Semantic Scholar
Upper Extremity Anomalies in Pfeiffer Syndrome and Mutational Correlations
F. Cerrato, Laura C. Nuzzi, Todd A. Theman, Amir H. Taghinia +2 more
2014Plastic and Reconstructive Surgery7 citations Open access
Semantic Scholar
Expression Analysis of Macrodactyly Identifies Pleiotrophin Upregulation
F. Lau, Fang Xia, Adam Kaplan, F. Cerrato +4 more
2012PLoS ONE7 citations Open access
Semantic Scholar
Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and SARS-CoV-2 variants
N. Welch, M. Zhu, C. Hua, J. Weller +31 more
2021medRxiv6 citations Open access
Semantic Scholar
Preoperative electrocardiograms for nonsyndromic children with hand syndactyly.
Laura C. Nuzzi, Carolyn M. Pike, Eliza B. Lewine, F. Cerrato +6 more
2015Journal of Hand Surgery-American Volume6 citations
Semantic Scholar
Reply: Psychological Impact of Breast Asymmetry on Adolescents: A Prospective Cohort.
Laura C. Nuzzi, F. Cerrato, M. Webb, Heather R. Faulkner +4 more
2015Plastic and Reconstructive Surgery3 citations Open access
Semantic Scholar
Author Correction: Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variants
N. Welch, Meilin Zhu, C. Hua, Juliane Weller +46 more
2023Nature Medicine2 citations Open access
Semantic Scholar
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals.
Joshua E. Motelow, G. Povysil, R. Dhindsa, Kate E. Stanley +251 more
2021American Journal of Human Genetics2 citations Open access
Semantic Scholar
The Genetics of Anxiety Disorders
J. Smoller, F. Cerrato, Sarah L. Weatherall
20151 citations
Semantic Scholar
A founder population reveals genetic variation with major effect on serious mental illness
Greta Gerdes, V. Tozzo, S. Service, C. Frydman-Gani +55 more
2026medRxiv0 citations Open access
Semantic Scholar
Schizophrenia Spectrum Biomarkers Consortium: Establishment of a Biorepository for the Discovery of Quantitative Fluid Biomarkers
Mohini Ranganathan, Susan G. Jakob, F. Cerrato, Lia Urban Spillane +24 more
2026Schizophrenia bulletin0 citations Open access
Semantic Scholar
Autism Sequencing Consortium (ASC) iPSYCH-BROAD Consortium Broad Institute Center for Common Disease Genomics (Broad-CCDG)
B. Aleksic, Joon-Yong Anney, R. Anney, M. Artomov +216 more
20210 citations
Semantic Scholar
Characterization Of Focal And Generalized Epilepsy Polygenic Burden In 630,603 Individuals
C. Leu, R. Stevelink, Alastair D. Smith, T. Richardson +27 more
20190 citations
Semantic Scholar

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