Search

Author/Creator Nicolas, Aude

1. A Meta‐Analysis of the Transferability of Bone Mineral Density Genetic Loci Associations From European to African Ancestry Populations. (18th December 2020)

Authors:
Yau, Michelle S; Kuipers, Allison L; Price, Ryan; Nicolas, Aude; Tajuddin, Salman M; Handelman, Samuel K; Arbeeva, Liubov; Chesi, Alessandra; Hsu, Yi‐Hsiang; Liu, Ching‐Ti; Karasik, David; Zemel, Babette S; Grant, Struan FA; Jordan, Joanne M; Jackson, Rebecca D; Evans, Michele K; Harris, Tamara B...
Journal:
Journal of bone and mineral research
Issue:
Volume 36:Number 3(2021)
Page Start:
469
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Rare missense variant (R251G) on APOE counterbalances the Alzheimer's disease risk associated with APOE‐ε4. (20th December 2022)

Authors:
Guen, Yann Le; Belloy, Michael E; Grenier‐Boley, Benjamin; de Rojas, Itziar; Castillo, Atahualpa; Jansen, Iris E; Nicolas, Aude; Bellenguez, Céline; Dalmasso, Carolina; Küçükali, Fahri; Eger, Sarah J; Álvarez‐Martínez, Victoria; Arosio, Beatrice; Benussi, Luisa; Boland, Anne; Borroni, Barbara; Bu...
Journal:
Alzheimer's & dementia
Issue:
Volume 18(2022)Supplement 4
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Protective association of HLA‐DRB1*04 subtypes in neurodegenerative diseases implicates acetylated tau PHF6 sequences. (20th December 2022)

Authors:
Guen, Yann Le; Luo, Guo; Ambati, Aditya; Damotte, Vincent; Jansen, Iris E; Yu, Eric; Nicolas, Aude; de Rojas, Itziar; Leal, Thiago Peixoto; Miyashita, Akinori; Bellenguez, Céline; Lian, Michelle Mulan; Parveen, Kayenat; Morizono, Takashi; Park, Hyeonseul; Grenier‐Boley, Benjamin; Naito, Tatsuhiko...
Journal:
Alzheimer's & dementia
Issue:
Volume 18(2022)Supplement 3
Page Start:
n/a
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis. Issue 4 (13th March 2019)

Authors:
Bandres‐Ciga, Sara; Noyce, Alastair J.; Hemani, Gibran; Nicolas, Aude; Calvo, Andrea; Mora, Gabriele; Tienari, Pentti J.; Stone, David J.; Nalls, Mike A.; Singleton, Andrew B.; Chiò, Adriano; Traynor, Bryan J.
Other Names:
Arosio Alessandro investigator.; Barberis Marco investigator.; Bartolomei Ilaria investigator.; Battistini Stefania investigator.; Benigni Michele investigator.; Borghero Giuseppe investigator.; Brunetti Maura investigator.; Calvo Andrea investigator.; Cammarosano Stefania investigator.; Cannas A...
Journal:
Annals of neurology
Issue:
Volume 85:Issue 4(2019)
Page Start:
470
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease. Issue 2 (14th September 2018)

Authors:
Kia, Demis A.; Noyce, Alastair J.; White, Jon; Speed, Doug; Nicolas, Aude; Burgess, Stephen; Lawlor, Debbie A.; Davey Smith, George; Singleton, Andrew; Nalls, Mike A.; Sofat, Reecha; Wood, Nicholas W.
Journal:
Annals of neurology
Issue:
Volume 84:Issue 2(2018)
Page Start:
191
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. (June 2015)

Authors:
Lesage, Suzanne; Bras, Jose; Cormier-Dequaire, Florence; Condroyer, Christel; Nicolas, Aude; Darwent, Lee; Guerreiro, Rita; Majounie, Elisa; Federoff, Monica; Heutink, Peter; Wood, Nicholas W.; Gasser, Thomas; Hardy, John; Tison, François; Singleton, Andrew; Brice, Alexis
Journal:
Neurology
Issue:
Volume 1:Number 1(2015)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

7. Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study. Issue 10 (October 2015)

Authors:
Nalls, Mike A; McLean, Cory Y; Rick, Jacqueline; Eberly, Shirley; Hutten, Samantha J; Gwinn, Katrina; Sutherland, Margaret; Martinez, Maria; Heutink, Peter; Williams, Nigel M; Hardy, John; Gasser, Thomas; Brice, Alexis; Price, T Ryan; Nicolas, Aude; Keller, Margaux F; Molony, Cliona; Gibbs, J Rap...
Journal:
Lancet neurology
Issue:
Volume 14:Issue 10(2015:Oct.)
Page Start:
1002
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

8. LRP10 in α-synucleinopathies. Issue 12 (December 2018)

Authors:
Kia, Demis A; Sabir, Marya S; Ahmed, Sarah; Trinh, Joanne; Bandres-Ciga, Sara; Noyce, Alastair J; Kaiyrzhanov, Rauan; Middlehurst, Ben; Kia, Demis A; Tan, Manuela; Houlden, Henry; Morris, Huw R; Plun-Favreau, Helene; Holmans, Peter; Hardy, John; Trabzuni, Daniah; Bras, Jose; Quinn, John; Mok, Kin...
Journal:
Lancet neurology
Issue:
Volume 17:Issue 12(2018)
Page Start:
1032
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

9. Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance. (18th October 2016)

Authors:
Lubbe, Steven J.; Escott-Price, Valentina; Gibbs, J. Raphael; Nalls, Mike A.; Bras, Jose; Price, T. Ryan; Nicolas, Aude; Jansen, Iris E.; Mok, Kin Y.; Pittman, Alan M.; Tomkins, James E.; Lewis, Patrick A.; Noyce, Alastair J.; Lesage, Suzanne; Sharma, Manu; Schiff, Elena R.; Levine, Adam P.; Bric...
Journal:
Human molecular genetics
Issue:
Volume 25:Number 24(2016:Dec. 15)
Page Start:
5483
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗