Meet ApplyKite Twin, the application assistant that learns with you

Meet your Twin, it learns with you

Your Twin learns with you

Launch week codes:30% off annual Pro20% off monthly Pro

Ends in00h00m00s

Andrea Accogli

Has grant

Medical Geneticist

McGill University

Canada

Research Interests

Explore related searches

Professors in Canada Professors in Medical Science Medical Science professors in Canada

Recent Grants

Grant: Open

RNA Helicase Dysfunction in Epilepsy: The Role of DHX15

Open Date: 2026-08-01

Close Date: 2027-07-01

Grant: Close

From Variant to Function to Therapeutics: An Integrative Framework for Neurodevelopmental Disorders

Open Date: 2026-06-01

Close Date:

Grant: Close

Rare Diseases: Models & Mechanisms (RDMM) Network – DHX15

Open Date: 2026-05-01

Close Date:

Grant: Close

Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation

Open Date: 2024-06-01

Close Date: 2024-06-01

Grant: Open

Unveiling New Genetic Players in Axon Guidance and neuronal migration Defects

Open Date: 2024-05-01

Close Date: 2027-04-30

Articles (20)

Year:

2026

Year:

2026

Year:

2026

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Collaborators (22)

Meena Balasubramanian

University of Sheffield

UNITED KINGDOM

View details

Christiane Zweier

Head

Inselspital Universitätsspital Bern

SWITZERLAND

View details

Myriam Srour

Associate Director, Azrieli Centre for Autism Research Clinic

McGill University

CANADA

View details

Mahshid Azamian

Baylor College of Medicine

UNITED STATES

View details

Phillip Grote

Goethe University Frankfurt

GERMANY

View details

Maurizio Delvecchio

Docenti di ruolo di IIa fascia

University of L'Aquila

ITALY

View details

Ernest Turro

Icahn School of Medicine at Mount Sinai

UNITED STATES

View details

Sally Ann Lynch

IRELAND

View details

Marzia Ognibene

Biologist

Istituto Giannina Gaslini

ITALY

View details

Guy M. Lenk

University of Michigan

UNITED STATES

View details

Seth Berger

Associate Professor

Children's National Health System

UNITED STATES

View details

Manuela Morleo

Assistant Professor

University of Campania “Luigi Vanvitelli”

ITALY

View details

William Dobyns

Professor

University of Minnesota

UNITED STATES

View details

Annalaura Torella

Ricercatore Universitario RTDA

Università degli Studi della Campania Luigi Vanvitelli

ITALY

View details

Louise Bicknell

Professor

University of Otago

NEW ZEALAND

View details

Christina Ringmann Fagerberg

Clinical Associate Professor

University of Southern Denmark

DENMARK

View details

roberta battini

University of Pisa

ITALY

View details

Laura Licchetta

University of Bologna

ITALY

View details

Cristina Dias

King’s College London

UNITED KINGDOM

View details

Markus Ries

Professor

UniversitätsKlinikum Heidelberg

GERMANY

View details

Mary Green

Deputy Head of Experimental Histopathology

The Francis Crick Institute

UNITED KINGDOM

View details

Christian Kubisch

Full Professor and Chair

University Medical Center Hamburg-Eppendorf (UKE)

GERMANY

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Andrea Accogli

Research Interests

Explore related searches

Recent Grants

Articles (20)

Cerebellar Abnormalities in the Neuroimaging Spectrum of CLTC-Related Disorder.

Telethon Undiagnosed Disease Program: Structured approach to solving rare childhood-onset genetic diseases

Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.

BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

Pathogenic variants in<i> TMEM184B</i> cause a neurodevelopmental syndrome associated with alteration of metabolic signaling

A mutational hotspot in TUBB2A associated with impaired heterodimer formation and severe brain developmental disorders

Reanalysis of Undiagnosed Neurodevelopmental Disorder Cases: From &lt;i&gt;RNU4-2&lt;/i&gt; Variants to Clinical Phenotypes.

Nanopore Sequencing Solves an Elusive Case of Sotos Syndrome.

Variants in the WDR44 WD40-repeat domain cause a spectrum of ciliopathy by impairing ciliogenesis initiation

Biallelic loss-of-function variants of SLC12A9 cause lysosome dysfunction and a syndromic neurodevelopmental disorder.

Clinical and molecular characterization of patients with YWHAG‐related epilepsy

Bi-allelic variants in <i>CELSR3</i> are implicated in central nervous system and urinary tract anomalies

Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivity.

A second hotspot for pathogenic exon-skipping variants in CDC45

Neurological and psychiatric phenotype of a multicenter cohort of patients with SETD5-related neurodevelopmental disorder.

Allelic heterogeneity and abnormal vesicle recycling in <i>PLAA</i>-related neurodevelopmental disorders.

Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation.

De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features.

Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected Individuals.

Biallelic loss-of-function variants in CACHD1 cause a novel neurodevelopmental syndrome with facial dysmorphism and multisystem congenital abnormalities.

Collaborators (22)

Meena Balasubramanian

Christiane Zweier

Myriam Srour

Mahshid Azamian

Phillip Grote

Maurizio Delvecchio

Ernest Turro

Sally Ann Lynch

Marzia Ognibene

Guy M. Lenk

Seth Berger

Manuela Morleo

William Dobyns

Annalaura Torella

Louise Bicknell

Christina Ringmann Fagerberg

roberta battini

Laura Licchetta

Cristina Dias

Markus Ries

Mary Green

Christian Kubisch

Make your next move.

Reanalysis of Undiagnosed Neurodevelopmental Disorder Cases: From <i>RNU4-2</i> Variants to Clinical Phenotypes.