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G. Cavalleri · SciRah

Researcher profile · Semantic Scholar

G. Cavalleri

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G. Cavalleri — researcher profile on SciRah

h-index: 51
Works: 286
Citations: 14K

Most-cited papers

The genetic architecture of the human cerebral cortex
K. Grasby, N. Jahanshad, J. Painter, L. Colodro-Conde +356 more
2020Science824 citations Open access
Semantic Scholar
Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study
C. Whelan, A. Altmann, J. Botía, N. Jahanshad +87 more
2018Brain : a journal of neurology494 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
Genetic architecture of subcortical brain structures in 38,851 individuals
C. Satizabal, H. Adams, D. Hibar, Charles C. White +285 more
2019Nature Genetics250 citations Open access
Semantic Scholar
White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA Epilepsy study
S. Hatton, Khoa H Huynh, L. Bonilha, E. Abela +72 more
2019bioRxiv216 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
Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study
S. Larivière, Raúl Rodríguez-Cruces, J. Royer, M. Caligiuri +58 more
2020Science Advances187 citations Open access
Semantic Scholar
Polygenic burden in focal and generalized epilepsies
C. Leu, R. Stevelink, Alexander W Smith, S. Goleva +16 more
2019Brain : a journal of neurology137 citations Open access
Semantic Scholar
Epilepsy in the mTORopathies: opportunities for precision medicine
P. Moloney, G. Cavalleri, N. Delanty
2021Brain Communications110 citations Open access
Semantic Scholar
Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression
S. Larivière, J. Royer, Raúl Rodríguez-Cruces, C. Paquola +70 more
2022Nature Communications104 citations Open access
Semantic Scholar
Ancient genomes from Iceland reveal the making of a human population
S. Ebenesersdóttir, Marcela Sandoval-Velasco, Ellen D. Gunnarsdóttir, Anuradha Jagadeesan +26 more
2018Science96 citations Open access
Semantic Scholar
Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
D. van der Meer, I. Sønderby, T. Kaufmann, G. Walters +128 more
2020JAMA psychiatry82 citations Open access
Semantic Scholar
The ENIGMA‐Epilepsy working group: Mapping disease from large data sets
S. Sisodiya, C. Whelan, S. Hatton, Khoa H Huynh +107 more
2020Human Brain Mapping81 citations Open access
Semantic Scholar
SJS/TEN 2019: From Science to Translation
Wan-Chun Chang, R. Abe, P. Anderson, Wanpen Anderson +66 more
2020Journal of dermatological science (Amsterdam)65 citations Open access
Semantic Scholar
Tackling Epilepsy With High-definition Precision Medicine: A Review.
H. Kearney, S. Byrne, G. Cavalleri, N. Delanty
2019JAMA Neurology62 citations
Semantic Scholar
The Epilepsy Genetics Initiative: Systematic reanalysis of diagnostic exomes increases yield
S. Berkovic, D. Goldstein, E. Heinzen, Brandon Laughlin +58 more
2019Epilepsia59 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
Long‐ and short‐term outcomes in renal allografts with deceased donors: A large recipient and donor genome‐wide association study
M. Hernandez-Fuentes, C. Franklin, I. Rebollo-Mesa, J. Mollon +41 more
2018American Journal of Transplantation53 citations Open access
Semantic Scholar
A comparison of genomic diagnostics in adults and children with epilepsy and comorbid intellectual disability
K. Benson, M. White, N. Allen, S. Byrne +23 more
2020European Journal of Human Genetics51 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
A systems-level analysis highlights microglial activation as a modifying factor in common epilepsies
A. Altmann, Mina Ryten, M. Di Nunzio, T. Ravizza +96 more
2021Neuropathology and Applied Neurobiology48 citations Open access
Semantic Scholar
The role of common genetic variation in presumed monogenic epilepsies
C. Campbell, C. Leu, Y. Feng, S. Wolking +20 more
2022EBioMedicine42 citations Open access
Semantic Scholar
Genetic and Clinical Predictors of Age of ESKD in Individuals With Autosomal Dominant Tubulointerstitial Kidney Disease Due to UMOD Mutations
K. Kidd, P. Vylet’al, C. Schaeffer, E. Olinger +38 more
2020Kidney International Reports42 citations Open access
Semantic Scholar
Comparative effectiveness of antiepileptic drugs in juvenile myoclonic epilepsy
K. Silvennoinen, Nikola Lange, S. Zagaglia, S. Balestrini +37 more
2019Epilepsia Open41 citations Open access
Semantic Scholar
The genetic landscape of Scotland and the Isles
Edmund H. Gilbert, Seamus O’Reilly, M. Merrigan, D. McGettigan +16 more
2019Proceedings of the National Academy of Sciences of the United States of America37 citations Open access
Semantic Scholar
Functional EPAS1/HIF2A missense variant is associated with hematocrit in Andean highlanders
E. Lawrence, W. Gu, Ryan J Bohlender, C. Anza-Ramirez +35 more
2024Science Advances36 citations Open access
Semantic Scholar
Updates in SJS/TEN: collaboration, innovation, and community
Madeline E Marks, Ramya Krishna Botta, Riichiro Abe, Thomas M. Beachkofsky +58 more
2023Frontiers in Medicine35 citations Open access
Semantic Scholar
The genetic history of Scandinavia from the Roman Iron Age to the present.
Ricardo Rodríguez-Varela, K. Moore, S. Ebenesersdóttir, G. Kılınç +40 more
2023Cell34 citations Open access
Semantic Scholar
The utility of a genetic kidney disease clinic employing a broad range of genomic testing platforms: experience of the Irish Kidney Gene Project
Elhussein A. E. Elhassan, S. Murray, D. Connaughton, C. Kennedy +18 more
2022JN. Journal of Nephrology (Milano. 1992)32 citations Open access
Semantic Scholar
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A
C. Steward, Jolien Roovers, M. Suner, J. Gonzalez +32 more
2019npj Genomic Medicine32 citations Open access
Semantic Scholar
Testing association of rare genetic variants with resistance to three common antiseizure medications
S. Wolking, Claudia Moreau, A. Nies, E. Schaeffeler +27 more
2020Epilepsia31 citations Open access
Semantic Scholar
Postictal Psychosis in Epilepsy: A Clinicogenetic Study
V. Braatz, Helena Martins Custodio, C. Leu, L. Agrò +16 more
2021Annals of Neurology30 citations Open access
Semantic Scholar
A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam
C. Campbell, M. McCormack, Sonn Patel, Caragh P. Stapleton +22 more
2022Epilepsia29 citations Open access
Semantic Scholar
Pharmacoresponse in genetic generalized epilepsy: a genome-wide association study.
S. Wolking, H. Schulz, A. Nies, M. McCormack +28 more
2020Pharmacogenomics (London)29 citations Open access
Semantic Scholar
Revealing the recent demographic history of Europe via haplotype sharing in the UK Biobank
Edmund H. Gilbert, Ashwini Shanmugam, G. Cavalleri
2022Proceedings of the National Academy of Sciences of the United States of America28 citations Open access
Semantic Scholar
Everolimus precision therapy for the GATOR1‐related epilepsies: A case series
P. Moloney, Hugh Kearney, K. Benson, D. Costello +4 more
2023European Journal of Neurology26 citations Open access
Semantic Scholar
Utility of genomic testing after renal biopsy
S. Murray, A. Dorman, K. Benson, D. Connaughton +14 more
2019American Journal of Nephrology26 citations Open access
Semantic Scholar
Population History and Altitude-Related Adaptation in the Sherpa
S. Bhandari, G. Cavalleri
2019Frontiers in Physiology26 citations Open access
Semantic Scholar
The population genomic legacy of the second plague pandemic
S. Gopalakrishnan, S. Ebenesersdóttir, I. Lundstrøm, G. Turner‐Walker +56 more
2022Current Biology25 citations Open access
Semantic Scholar
Assessing the role of rare genetic variants in drug‐resistant, non‐lesional focal epilepsy
S. Wolking, Claudia Moreau, M. McCormack, R. Krause +20 more
2021Annals of Clinical and Translational Neurology23 citations Open access
Semantic Scholar
Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy
B. Park, S. Larivière, Raúl Rodríguez-Cruces, J. Royer +83 more
2021Brain : a journal of neurology21 citations Open access
Semantic Scholar
An Exome Sequencing Study of 10 Families with IgA Nephropathy
Caragh P. Stapleton, C. Kennedy, N. Fennelly, S. Murray +5 more
2019Nephron21 citations Open access
Semantic Scholar
The impact of donor and recipient common clinical and genetic variation on estimated glomerular filtration rate in a European renal transplant population.
Caragh P. Stapleton, A. Heinzel, W. Guan, Peter J. Most +75 more
2019American Journal of Transplantation21 citations Open access
Semantic Scholar
Role of Common Genetic Variants for Drug-Resistance to Specific Anti-Seizure Medications
S. Wolking, C. Campbell, Caragh P. Stapleton, M. McCormack +14 more
2021Frontiers in Pharmacology20 citations Open access
Semantic Scholar
Exploring the genetic overlap between psychiatric illness and epilepsy: A review.
C. Campbell, G. Cavalleri, N. Delanty
2019Epilepsy & Behavior20 citations Open access
Semantic Scholar
Genome-wide association meta-analyses of drug-resistant epilepsy
C. Leu, Andreja Avbersek, R. Stevelink, H. M. Custodio +29 more
2025EBioMedicine19 citations Open access
Semantic Scholar
Genomic and clinical predictors of lacosamide response in refractory epilepsies
S. Heavin, M. McCormack, S. Wolking, Lisa Slattery +25 more
2019Epilepsia Open18 citations Open access
Semantic Scholar
Genome-wide meta-analysis of over 29,000 people with epilepsy reveals 26 loci and subtype-specific genetic architecture
International League Against Epilepsy Consortium o, S. Berkovic, G. Cavalleri, B. Koeleman
2022medRxiv17 citations Open access
Semantic Scholar
The genetic landscape of polycystic kidney disease in Ireland
K. Benson, S. Murray, Sarah R. Senum, Elhussein A. E. Elhassan +18 more
2021European Journal of Human Genetics17 citations Open access
Semantic Scholar
Polygenic risk score of non-melanoma skin cancer predicts post-transplant skin cancer across multiple organ types.
Caragh P. Stapleton, B. Chang, B. Keating, P. Conlon +1 more
2020Clinical Transplantation14 citations Open access
Semantic Scholar

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