Céline Bellenguez

Springer Nature publications

• Article

  APOE-stratified genome-wide association analyses provide insights into the genetic etiology of Alzheimers’s disease

  • Jesper Qvist Thomassen
  • Hampton Leonard
  • Ruth Frikke-Schmidt

  in Nature Genetics

  14 September 2026 Open Access

  
• Article

  PLCG2 downregulation impairs synaptic function and increases Alzheimer’s disease hallmarks in neuronal cultures

  • Audrey Coulon
  • Florian Rabiller
  • Jean-Charles Lambert

  in Nature Genetics

  14 August 2026 Open Access

  
• Article

  Consensus meta-analysis of genome-wide association studies for Alzheimer’s disease and related dementias

  • Céline Bellenguez
  • Atahualpa Castillo Morales
  • Geir Bråthen

  in Nature Genetics

  3 June 2026 Open Access

  
• Article

  Assessing the de novo paradigm in sporadic early-onset Alzheimer disease trios

  • Aline Zarea
  • Kevin Cassinari
  • Gaël Nicolas

  in Molecular Psychiatry

  29 May 2026 Open Access

  
• Article

  GWAS meta-analysis of cerebrospinal fluid Alzheimer’s biomarkers reveals loci regulating lipids, brain volume and autophagy

  • Jigyasha Timsina
  • Chenyang Jiang
  • Carlos Cruchaga

  in Nature Communications

  21 April 2026 Open Access

  
• Article

  Machine learning in Alzheimer’s disease genetics

  • Matthew Bracher-Smith
  • Federico Melograna
  • Mohammad Arfan Ikram

  in Nature Communications

  22 July 2025 Open Access

  
• Article

  Transferability of European-derived Alzheimer’s disease polygenic risk scores across multiancestry populations

  • Aude Nicolas
  • Richard Sherva
  • Jean-Charles Lambert

  in Nature Genetics

  18 June 2025 Open Access

  
• Article

  Monoallelic TYROBP deletion is a novel risk factor for Alzheimer’s disease

  • Henna Martiskainen
  • Roosa-Maria Willman
  • Petri Lehto

  in Molecular Neurodegeneration

  29 April 2025 Open Access

  
• Article

  Low prevalence of CWH43 variants among Finnish and Norwegian idiopathic normal pressure hydrocephalus patients: a cohort-based observational study

  • Joel Räsänen
  • Seppo Helisalmi
  • Anssi Lipponen

  in Fluids and Barriers of the CNS

  13 February 2025 Open Access

  
• Article

  X‐chromosome-wide association study for Alzheimer’s disease

  • Julie Le Borgne
  • Lissette Gomez
  • Céline Bellenguez

  in Molecular Psychiatry

  4 December 2024 Open Access

  
• Article

  How local reference panels improve imputation in French populations

  • Anthony F. Herzig
  • Lourdes Velo‐Suárez
  • Véronique Geoffroy

  in Scientific Reports

  3 January 2024 Open Access

  
• Article

  Step by step: towards a better understanding of the genetic architecture of Alzheimer’s disease

  • Jean-Charles Lambert
  • Alfredo Ramirez
  • Céline Bellenguez

  in Molecular Psychiatry

  2 May 2023 Open Access

  
• Article

  Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

  • Itziar de Rojas
  • Sonia Moreno-Grau
  • Arvid Rongve

  in Nature Communications

  9 February 2023 Open Access
• Article

  Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease

  • Henne Holstege
  • Marc Hulsman
  • Jean-Charles Lambert

  in Nature Genetics

  21 November 2022 Open Access

  
• Article

  Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

  • Iris E. Jansen
  • Sven J. van der Lee
  • Wiesje van der Flier

  in Acta Neuropathologica

  6 September 2022 Open Access

  
• Article

  New insights into the genetic etiology of Alzheimer’s disease and related dementias

  • Céline Bellenguez
  • Fahri Küçükali
  • Jean-Charles Lambert

  in Nature Genetics

  4 April 2022 Open Access

  
• Article

  Genetics of PlGF plasma levels highlights a role of its receptors and supports the link between angiogenesis and immunity

  • Daniela Ruggiero
  • Teresa Nutile
  • Marina Ciullo

  in Scientific Reports

  19 August 2021 Open Access

  
• Article

  Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores

  • Itziar de Rojas
  • Sonia Moreno-Grau
  • Arvid Rongve

  in Nature Communications

  7 June 2021 Open Access

  
• Article

  Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluation

  • Olivier Quenez
  • Kevin Cassinari
  • Doris Lechner

  in European Journal of Human Genetics

  26 June 2020

  
• Article

  Complement genes contribute sex-biased vulnerability in diverse disorders

  • Nolan Kamitaki
  • Aswin Sekar
  • Michael C. O’Donovan

  in Nature

  11 May 2020

  
• Article

  Correction: Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

  • Joshua C. Bis
  • Xueqiu Jian
  • Lindsay A. Farrer

  in Molecular Psychiatry

  21 October 2019 Open Access
• Article

  A polygenic resilience score moderates the genetic risk for schizophrenia

  • Jonathan L. Hess
  • Daniel S. Tylee
  • Fritz Zimprich

  in Molecular Psychiatry

  6 September 2019 Open Access

  
• Article

  Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

  • Brian W. Kunkle
  • Benjamin Grenier-Boley
  • Margaret A. Pericak-Vance

  in Nature Genetics

  15 August 2019
• Article

  Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

  • Alberto Romagnoni
  • Simon Jégou
  • Pamela Whittaker

  in Scientific Reports

  17 July 2019 Open Access

  
• Article

  Whole-Exome Sequencing in the Isolated Populations of Cilento from South Italy

  • T. Nutile
  • D. Ruggiero
  • M. Ciullo

  in Scientific Reports

  11 March 2019 Open Access

  
• Article

  Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

  • Brian W. Kunkle
  • Benjamin Grenier-Boley
  • Margaret A. Pericak-Vance

  in Nature Genetics

  28 February 2019

  
• Article

  Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease

  • Maria Carolina Dalmasso
  • Luis Ignacio Brusco
  • Alfredo Ramirez

  in Translational Psychiatry

  31 January 2019 Open Access

  
• Article

  Whole exome sequencing study identifies novel rare and common Alzheimer’s-Associated variants involved in immune response and transcriptional regulation

  • Joshua C. Bis
  • Xueqiu Jian
  • Lindsay A. Farrer

  in Molecular Psychiatry

  14 August 2018 Open Access

  
• Article

  Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

  • Milly S. Tedja
  • Robert Wojciechowski
  • Caroline C. W. Klaver

  in Nature Genetics

  28 May 2018

  
• Article

  Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

  • Adriana I. Iglesias
  • Aniket Mishra
  • Pamela Whittaker

  in Nature Communications

  14 May 2018 Open Access

  
• Chapter

  Genetic Risk Factors for Complex Forms of Alzheimer’s Disease

  • Céline Bellenguez
  • Jean-Charles Lambert

  in Neurodegenerative Diseases

  1 January 2018

  
• Article

  Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

  • Rebecca Sims
  • Sven J van der Lee
  • Gerard D Schellenberg

  in Nature Genetics

  17 July 2017

  
• Article

  Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians

  • Stéphanie Guey
  • Markus Kraemer
  • Lechner D

  in European Journal of Human Genetics

  21 June 2017

  
• Article

  A common haplotype lowers PU.1 expression in myeloid cells and delays onset of Alzheimer's disease

  • Kuan-lin Huang
  • Edoardo Marcora
  • Alison M Goate

  in Nature Neuroscience

  19 June 2017

  
• Article

  MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls

  • D Cosgrove
  • D Harold
  • Pamela Whittaker

  in Translational Psychiatry

  24 January 2017 Open Access

  
• Article

  17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression

  • K Le Guennec
  • O Quenez
  • A Rovelet-Lecrux

  in Molecular Psychiatry

  13 December 2016

  
• Article

  Accuracy of heritability estimations in presence of hidden population stratification

  • Claire Dandine-Roulland
  • Céline Bellenguez
  • Hervé Perdry

  in Scientific Reports

  25 May 2016 Open Access

  
• Article

  Exome-wide study of ankylosing spondylitis demonstrates additional shared genetic background with inflammatory bowel disease

  • Philip C Robinson
  • Paul J Leo
  • Chris CA Spencer

  in npj Genomic Medicine

  4 May 2016 Open Access
• Article

  Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology

  • P Dourlen
  • F J Fernandez-Gomez
  • B Dermaut

  in Molecular Psychiatry

  26 April 2016 Open Access

  
• Article

  Meta-analysis of gene–environment-wide association scans accounting for education level identifies additional loci for refractive error

  • Qiao Fan
  • Virginie J. M. Verhoeven
  • Kari Matti Mäkelä

  in Nature Communications

  6 April 2016 Open Access