Gianpiero Cavalleri

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Professor of Human Genetics

Ireland

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About

Gianpiero Cavalleri is a Professor of Human Genetics at the Royal College of Surgeons in Ireland School of Medicine. His research focuses on the genetics of complex conditions, including neurological disorders and kidney diseases. Recent articles authored by Professor Cavalleri explore topics such as the gut microbiome's role in encephalitis, genetic variants influencing kidney function, and the demographic history of Ireland and Britain.

Recent Grants

Grant: Close

Blockchain-enabled clinical trials stratification system (BESTS)

Open Date: 2020-03-01

Close Date: 2023-02-01

Grant: Close

The Centre for Research Training in Genomics Data Sciences

Open Date: 2019-02-01

Close Date: 2026-08-01

Grant: Close

The FutureNeuro Research Centre

Open Date: 2018-11-01

Close Date: 2024-10-01

Articles (28)

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Collaborators (46)

Heidi Kirsch

Professor of Clinical Neurology and Radiology & Biomedical Imaging

UCSF Medical Center

UNITED STATES

Gianpiero Cavalleri

Research Interests

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About

Recent Grants

Articles (28)

A genetic perspective on the recent demographic history of Ireland and Britain

The gut microbiome associated with LGI1‐antibody encephalitis

Genome-wide association meta-analyses of drug-resistant epilepsy

Donor and Recipient Polygenic Risk Scores Influence Kidney Transplant Function.

Polygenic risk scores for eGFR are associated with age at kidney failure.

The impact of a secondary, rare, non-pathogenic PKD1 variant on disease progression in autosomal dominant polycystic kidney disease.

Adaptive &lt;i&gt;PRKAA1&lt;/i&gt; variant in Andeans is associated with improved ventilation and sleep phenotypes.

Characterization of Monogenic Kidney Disease in Older Patients With CKD.

Phenotypic outcomes of PKD1 compared with non-PKD1 genetically confirmed autosomal dominant polycystic kidney disease.

Novel risk loci in LGI1-antibody encephalitis: genome-wide association study discovery and validation cohorts

GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Screening medical students for SARS-CoV-2 to facilitate face-to-face clinical teaching and prevent onward spread to patients

Differential diagnosis of familial adult myoclonic epilepsy

Rare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy

The genetic history of Scandinavia from the Roman Iron Age to the present

Updates in SJS/TEN: collaboration, innovation, and community

Testing for pharmacogenomic predictors of ppRNFL thinning in individuals exposed to vigabatrin.

Everolimus precision therapy for the GATOR1-related epilepsies: A case series.

The Newfoundland and Labrador mosaic founder population descends from an Irish and British diaspora from 300 years ago.

Educating pharmacy students through a pandemic: Reflecting on our COVID-19 experience

A systems‐level analysis highlights microglial activation as a modifying factor in common epilepsies

A pharmacogenomic assessment of psychiatric adverse drug reactions to levetiracetam

Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study

Genomic analysis of "microphenotypes" in epilepsy

Germline mosaicism in a family with &lt;i&gt;MBD5&lt;/i&gt; haploinsufficiency

KBG syndrome mimicking genetic generalized epilepsy

Population history and genome wide association studies of birth weight in a native high altitude Ladakhi population

Collaborators (46)

Heidi Kirsch

Christian Rummel

Edmund Gilbert

Andrea Cherubini

Shyam Gopalakrishnan

fidelma fitzpatrick

Claire Hill

Julie Absil

James Barlow

Sarah Weckhuysen

Chiara De Santi

Eleonora Palma

Patricia Dugan

Andre Altmann

Ricardo Rodríguez-Varela

Katrina Peariso

Ingrid Kockum

Maria Eugenia Caligiuri

Arjune Sen

Caroline Cusick

Russell McLaughlin

Brian Kirby

Patrick Moloney

Walter Bodmer

Lucy Vivash

Shane Cullinan

Karl Martin Klein

Martin Krenn

Colin Doherty

Stefano Meletti

Toshimitsu Suzuki

Suman Pakala

Judith Strawbridge

Sophie N M Binks

Ingrid Scheffer

Rossella Di Sapia

Gabriele Ruffolo

Kazuhiro Yamakawa

Samuel Berkovic

Stefan Wolking

Fiona O'Brien

Anne McIntosh

Patxi Pérez-Ramallo

Doug Speed

Thomas Thesen

Adaptive <i>PRKAA1</i> variant in Andeans is associated with improved ventilation and sleep phenotypes.

Germline mosaicism in a family with <i>MBD5</i> haploinsufficiency