| Year |
Citation |
Score |
| 2023 |
Grangeon L, Charbonnier C, Zarea A, Rousseau S, Rovelet-Lecrux A, Bendetowicz D, Lemaitre M, Malrain C, Quillard-Muraine M, Cassinari K, Maltete D, Pariente J, Moreaud O, Magnin E, Cretin B, ... ... Campion D, et al. Phenotype and imaging features associated with APP duplications. Alzheimer's Research & Therapy. 15: 93. PMID 37170141 DOI: 10.1186/s13195-023-01172-2 |
0.685 |
|
| 2022 |
Holstege H, Hulsman M, Charbonnier C, Grenier-Boley B, Quenez O, Grozeva D, van Rooij JGJ, Sims R, Ahmad S, Amin N, Norsworthy PJ, Dols-Icardo O, Hummerich H, Kawalia A, Amouyel P, ... ... Campion D, et al. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature Genetics. PMID 36411364 DOI: 10.1038/s41588-022-01208-7 |
0.323 |
|
| 2022 |
Miguel L, Rovelet-Lecrux A, Chambon P, Joly-Helas G, Rousseau S, Wallon D, Epelbaum S, Frébourg T, Campion D, Nicolas G, Lecourtois M. Generation of 17q21.31 duplication iPSC-derived neurons as a model for primary tauopathies. Stem Cell Research. 61: 102762. PMID 35358831 DOI: 10.1016/j.scr.2022.102762 |
0.819 |
|
| 2022 |
Nicolas G, Sévigny M, Lecoquierre F, Marguet F, Deschênes A, Del Pelaez MC, Feuillette S, Audebrand A, Lecourtois M, Rousseau S, Richard AC, Cassinari K, Deramecourt V, Duyckaerts C, Boland A, ... ... Campion D, et al. A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics. Acta Neuropathologica Communications. 10: 20. PMID 35151370 DOI: 10.1186/s40478-022-01314-x |
0.822 |
|
| 2021 |
Rovelet-Lecrux A, Feuillette S, Miguel L, Schramm C, Pernet S, Quenez O, Ségalas-Milazzo I, Guilhaudis L, Rousseau S, Riou G, Frébourg T, Campion D, Nicolas G, Lecourtois M. Impaired SorLA maturation and trafficking as a new mechanism for SORL1 missense variants in Alzheimer disease. Acta Neuropathologica Communications. 9: 196. PMID 34922638 DOI: 10.1186/s40478-021-01294-4 |
0.807 |
|
| 2021 |
Grangeon L, Cassinari K, Rousseau S, Croisile B, Formaglio M, Moreaud O, Boutonnat J, Le Meur N, Miné M, Coste T, Pipiras E, Tournier-Lasserve E, Rovelet-Lecrux A, Campion D, Wallon D, et al. Early-Onset Cerebral Amyloid Angiopathy and Alzheimer Disease Related to an APP Locus Triplication. Neurology. Genetics. 7: e609. PMID 34532568 DOI: 10.1212/NXG.0000000000000609 |
0.69 |
|
| 2021 |
Wallon D, Boluda S, Rovelet-Lecrux A, Thierry M, Lagarde J, Miguel L, Lecourtois M, Bonnevalle A, Sarazin M, Bottlaender M, Mula M, Marty S, Nakamura N, Schramm C, Sellal F, ... ... Campion D, et al. Clinical and neuropathological diversity of tauopathy in MAPT duplication carriers. Acta Neuropathologica. PMID 34095977 DOI: 10.1007/s00401-021-02320-4 |
0.801 |
|
| 2020 |
Quenez O, Cassinari K, Coutant S, Lecoquierre F, Le Guennec K, Rousseau S, Richard AC, Vasseur S, Bouvignies E, Bou J, Lienard G, Manase S, Fourneaux S, Drouot N, Nguyen-Viet V, ... ... Campion D, et al. Detection of copy-number variations from NGS data using read depth information: a diagnostic performance evaluation. European Journal of Human Genetics : Ejhg. PMID 32591635 DOI: 10.1038/S41431-020-0672-2 |
0.637 |
|
| 2020 |
Cassinari K, Rovelet-Lecrux A, Tury S, Quenez O, Richard AC, Charbonnier C, Olaso R, Boland A, Deleuze JF, Besancenot JF, Delpont B, Pouliquen D, Lecoquierre F, Chambon P, Thauvin-Robinet C, ... Campion D, et al. Haploinsufficiency of the Primary Familial Brain Calcification Gene SLC20A2 Mediated by Disruption of a Regulatory Element. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 32506582 DOI: 10.1002/Mds.28090 |
0.703 |
|
| 2020 |
Feuillette S, Charbonnier C, Frebourg T, Campion D, Lecourtois M. A Connected Network of Interacting Proteins Is Involved in Human-Tau Toxicity in . Frontiers in Neuroscience. 14: 68. PMID 32116515 DOI: 10.3389/Fnins.2020.00068 |
0.788 |
|
| 2020 |
Miguel L, Frebourg T, Campion D, Lecourtois M. Moderate Overexpression of Tau in Drosophila Exacerbates Amyloid-β-Induced Neuronal Phenotypes and Correlates with Tau Oligomerization. Journal of Alzheimer's Disease : Jad. PMID 32065789 DOI: 10.3233/Jad-190906 |
0.804 |
|
| 2020 |
Chilton I, Okur V, Vitiello G, Selicorni A, Mariani M, Goldenberg A, Husson T, Campion D, Lichtenbelt KD, van Gassen K, Steinraths M, Rice J, Roeder ER, Littlejohn RO, Srour M, et al. De novo heterozygous missense and loss-of-function variants in CDC42BPB are associated with a neurodevelopmental phenotype. American Journal of Medical Genetics. Part A. PMID 32031333 DOI: 10.1002/Ajmg.A.61505 |
0.37 |
|
| 2019 |
Miguel L, Rovelet-Lecrux A, Feyeux M, Frebourg T, Nassoy P, Campion D, Lecourtois M. Detection of all adult Tau isoforms in a 3D culture model of iPSC-derived neurons. Stem Cell Research. 40: 101541. PMID 31522011 DOI: 10.1016/J.Scr.2019.101541 |
0.787 |
|
| 2019 |
Lacour M, Quenez O, Rovelet-Lecrux A, Salomon B, Rousseau S, Richard AC, Quillard-Muraine M, Pasquier F, Rollin-Sillaire A, Martinaud O, Zarea A, de la Sayette V, Boutoleau-Bretonniere C, Etcharry-Bouyx F, Chauviré V, ... ... Campion D, et al. Causative Mutations and Genetic Risk Factors in Sporadic Early Onset Alzheimer's Disease Before 51 Years. Journal of Alzheimer's Disease : Jad. PMID 31381512 DOI: 10.3233/Jad-190193 |
0.736 |
|
| 2019 |
Cassinari K, Quenez O, Joly-Hélas G, Beaussire L, Le Meur N, Castelain M, Goldenberg A, Guerrot AM, Brehin AC, Deleuze JF, Boland A, Rovelet-Lecrux A, Campion D, Saugier-Veber P, Gruchy N, et al. A Simple, Universal, and Cost-Efficient Digital PCR Method for the Targeted Analysis of Copy Number Variations. Clinical Chemistry. PMID 31292136 DOI: 10.1373/Clinchem.2019.304246 |
0.64 |
|
| 2019 |
Grangeon L, Wallon D, Charbonnier C, Quenez O, Richard AC, Rousseau S, Budowski C, Lebouvier T, Corbille AG, Vidailhet M, Méneret A, Roze E, Anheim M, Tranchant C, Favrole P, ... ... Campion D, et al. Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype. Brain : a Journal of Neurology. PMID 31009047 DOI: 10.1093/Brain/Awz095 |
0.706 |
|
| 2019 |
Campion D, Charbonnier C, Nicolas G. SORL1 genetic variants and Alzheimer disease risk: a literature review and meta-analysis of sequencing data. Acta Neuropathologica. PMID 30911827 DOI: 10.1007/S00401-019-01991-4 |
0.446 |
|
| 2019 |
Boscher E, Husson T, Quenez O, Laquerrière A, Marguet F, Cassinari K, Wallon D, Martinaud O, Charbonnier C, Nicolas G, Deleuze JF, Boland A, Lathrop M, Frébourg T, ... Campion D, et al. Copy Number Variants in miR-138 as a Potential Risk Factor for Early-Onset Alzheimer's Disease. Journal of Alzheimer's Disease : Jad. PMID 30909216 DOI: 10.3233/Jad-180940 |
0.681 |
|
| 2018 |
Pons M, Prieto S, Miguel L, Frebourg T, Campion D, Suñé C, Lecourtois M. Identification of TCERG1 as a new genetic modulator of TDP-43 production in Drosophila. Acta Neuropathologica Communications. 6: 138. PMID 30541625 DOI: 10.1186/S40478-018-0639-5 |
0.775 |
|
| 2018 |
Husson T, Duboc JB, Quenez O, Charbonnier C, Rotharmel M, Cuenca M, Jegouzo X, Richard AC, Frebourg T, Deleuze JF, Boland A, Genin E, Debette S, Tzourio C, Campion D, et al. Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing. Translational Psychiatry. 8: 268. PMID 30518751 DOI: 10.1038/S41398-018-0291-7 |
0.388 |
|
| 2018 |
Nicolas G, Acuna-Hidalgo R, Keogh MJ, Quenez O, Steehouwer M, Lelieveld S, Rousseau S, Richard AC, Oud MS, Marguet F, Laquerrière A, Morris CM, Attems J, Smith C, Ansorge O, ... ... Campion D, et al. Somatic variants in autosomal dominant genes are a rare cause of sporadic Alzheimer's disease. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 30114415 DOI: 10.1016/J.Jalz.2018.06.3056 |
0.474 |
|
| 2018 |
Bis JC, Jian X, Kunkle BW, Chen Y, Hamilton-Nelson KL, Bush WS, Salerno WJ, Lancour D, Ma Y, Renton AE, Marcora E, Farrell JJ, Zhao Y, Qu L, Ahmad S, ... ... Campion D, et al. Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry. PMID 30108311 DOI: 10.1038/S41380-018-0112-7 |
0.442 |
|
| 2018 |
Ramos EM, Carecchio M, Lemos R, Ferreira J, Legati A, Sears RL, Hsu SC, Panteghini C, Magistrelli L, Salsano E, Esposito S, Taroni F, Richard AC, Tranchant C, Anheim M, ... ... Campion D, et al. Primary brain calcification: an international study reporting novel variants and associated phenotypes. European Journal of Human Genetics : Ejhg. PMID 29955172 DOI: 10.1038/S41431-018-0185-4 |
0.367 |
|
| 2018 |
Miguel L, Avequin T, Pons M, Frébourg T, Campion D, Lecourtois M. FTLD/ALS-linked TDP-43 mutations do not alter TDP-43's ability to self-regulate its expression in Drosophila. Brain Research. PMID 29778779 DOI: 10.1016/J.Brainres.2018.05.021 |
0.789 |
|
| 2018 |
Le Guennec K, Tubeuf H, Hannequin D, Wallon D, Quenez O, Rousseau S, Richard AC, Deleuze JF, Boland A, Frebourg T, Gaildrat P, Campion D, Martins A, Nicolas G. Biallelic Loss of Function of SORL1 in an Early Onset Alzheimer's Disease Patient. Journal of Alzheimer's Disease : Jad. 62: 821-831. PMID 29480197 DOI: 10.3233/Jad-170981 |
0.414 |
|
| 2017 |
Nicolas G, Charbonnier C, Campion D, Veltman JA. Estimation of minimal disease prevalence from population genomic data: Application to primary familial brain calcification. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 29152850 DOI: 10.1002/Ajmg.B.32605 |
0.354 |
|
| 2017 |
Pons M, Miguel L, Miel C, Avequin T, Juge F, Frebourg T, Campion D, Lecourtois M. Splicing factors act as genetic modulators of TDP-43 production in a new autoregulatory TDP-43 Drosophila model. Human Molecular Genetics. 26: 3396-3408. PMID 28854702 DOI: 10.1093/Hmg/Ddx229 |
0.773 |
|
| 2017 |
Bellenguez C, Charbonnier C, Grenier-Boley B, Quenez O, Le Guennec K, Nicolas G, Chauhan G, Wallon D, Rousseau S, Richard AC, Boland A, Bourque G, Munter HM, Olaso R, Meyer V, ... ... Campion D, et al. Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls. Neurobiology of Aging. PMID 28789839 DOI: 10.1016/J.Neurobiolaging.2017.07.001 |
0.444 |
|
| 2017 |
Le Guennec K, Veugelen S, Quenez O, Szaruga M, Rousseau S, Nicolas G, Wallon D, Fluchere F, Frébourg T, De Strooper B, Campion D, Chávez-Gutiérrez L, Rovelet-Lecrux A. Deletion of exons 9 and 10 of the Presenilin 1 gene in a patient with Early-onset Alzheimer Disease generates longer amyloid seeds. Neurobiology of Disease. PMID 28461250 DOI: 10.1016/J.Nbd.2017.04.020 |
0.738 |
|
| 2017 |
Feuillette S, Delarue M, Riou G, Gaffuri AL, Wu J, Lenkei Z, Boyer O, Frébourg T, Campion D, Lecourtois M. Neuron-to-Neuron Transfer of FUS in Drosophila Primary Neuronal Culture Is Enhanced by ALS-Associated Mutations. Journal of Molecular Neuroscience : Mn. PMID 28429234 DOI: 10.1007/S12031-017-0908-Y |
0.775 |
|
| 2017 |
Lanoiselée HM, Nicolas G, Wallon D, Rovelet-Lecrux A, Lacour M, Rousseau S, Richard AC, Pasquier F, Rollin-Sillaire A, Martinaud O, Quillard-Muraine M, de la Sayette V, Boutoleau-Bretonniere C, Etcharry-Bouyx F, Chauviré V, ... ... Campion D, et al. APP, PSEN1, and PSEN2 mutations in early-onset Alzheimer disease: A genetic screening study of familial and sporadic cases. Plos Medicine. 14: e1002270. PMID 28350801 DOI: 10.1371/Journal.Pmed.1002270 |
0.743 |
|
| 2016 |
Nicolas G, Charbonnier C, Campion D. From Common to Rare Variants: The Genetic Component of Alzheimer Disease. Human Heredity. 81: 129-141. PMID 28002825 DOI: 10.1159/000452256 |
0.469 |
|
| 2016 |
Le Guennec K, Quenez O, Nicolas G, Wallon D, Rousseau S, Richard AC, Alexander J, Paschou P, Charbonnier C, Bellenguez C, Grenier-Boley B, Lechner D, Bihoreau MT, Olaso R, Boland A, ... ... Campion D, et al. 17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression. Molecular Psychiatry. PMID 27956742 DOI: 10.1038/Mp.2016.226 |
0.721 |
|
| 2016 |
Sellal F, Wallon D, Martinez-Almoyna L, Marelli C, Dhar A, Oesterlé H, Rovelet-Lecrux A, Rousseau S, Kourkoulis CE, Rosand J, DiPucchio ZY, Frosch M, Gombert C, Audoin B, Mine M, ... ... Campion D, et al. APP Mutations in Cerebral Amyloid Angiopathy with or without Cortical Calcifications: Report of Three Families and a Literature Review. Journal of Alzheimer's Disease : Jad. PMID 27858710 DOI: 10.3233/Jad-160709 |
0.715 |
|
| 2016 |
Pottier C, Ravenscroft TA, Brown PH, Finch NA, Baker M, Parsons M, Asmann YW, Ren Y, Christopher E, Levitch D, van Blitterswijk M, Cruchaga C, Campion D, Nicolas G, Richard AC, et al. TYROBP genetic variants in early-onset Alzheimer's disease. Neurobiology of Aging. PMID 27658901 DOI: 10.1016/J.Neurobiolaging.2016.07.028 |
0.37 |
|
| 2016 |
Zarea A, Charbonnier C, Rovelet-Lecrux A, Nicolas G, Rousseau S, Borden A, Pariente J, Le Ber I, Pasquier F, Formaglio M, Martinaud O, Rollin-Sillaire A, Sarazin M, Croisile B, Boutoleau-Bretonnière C, ... ... Campion D, et al. Seizures in dominantly inherited Alzheimer disease. Neurology. PMID 27466472 DOI: 10.1212/Wnl.0000000000003048 |
0.684 |
|
| 2016 |
David S, Ferreira J, Quenez O, Rovelet-Lecrux A, Richard AC, Vérin M, Jurici S, Le Ber I, Boland A, Deleuze JF, Frebourg T, Mendes de Oliveira JR, Hannequin D, Campion D, Nicolas G. Identification of partial SLC20A2 deletions in primary brain calcification using whole-exome sequencing. European Journal of Human Genetics : Ejhg. PMID 27245298 DOI: 10.1038/Ejhg.2016.50 |
0.688 |
|
| 2016 |
Dumanski JP, Lambert JC, Rasi C, Giedraitis V, Davies H, Grenier-Boley B, Lindgren CM, Campion D, Dufouil C, Pasquier F, Amouyel P, Lannfelt L, Ingelsson M, Kilander L, et al. Mosaic Loss of Chromosome Y in Blood Is Associated with Alzheimer Disease. American Journal of Human Genetics. PMID 27231129 DOI: 10.1016/J.Ajhg.2016.05.014 |
0.389 |
|
| 2016 |
Anheim M, López-Sánchez U, Giovannini D, Richard AC, Touhami J, N'Guyen L, Rudolf G, Thibault-Stoll A, Frebourg T, Hannequin D, Campion D, Battini JL, Sitbon M, Nicolas G. XPR1 mutations are a rare cause of primary familial brain calcification. Journal of Neurology. PMID 27230854 DOI: 10.1007/S00415-016-8166-4 |
0.395 |
|
| 2016 |
Le Guennec K, Nicolas G, Quenez O, Charbonnier C, Wallon D, Bellenguez C, Grenier-Boley B, Rousseau S, Richard AC, Rovelet-Lecrux A, Bacq D, Garnier JG, Olaso R, Boland A, Meyer V, ... ... Campion D, et al. ABCA7 rare variants and Alzheimer disease risk. Neurology. PMID 27037229 DOI: 10.1212/Wnl.0000000000002627 |
0.701 |
|
| 2016 |
Campion D, Pottier C, Nicolas G, Le Guennec K, Rovelet-Lecrux A. Alzheimer disease: modeling an Aβ-centered biological network. Molecular Psychiatry. PMID 27021818 DOI: 10.1038/Mp.2016.38 |
0.721 |
|
| 2016 |
Richard AC, Rovelet-Lecrux A, Delaby E, Charbonnier C, Thiruvahindrapuram B, Hatchwell E, Eis PS, Afenjar A, Dussardier BG, Scherer SW, Betancur C, Campion D. The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 26978485 DOI: 10.1002/Ajmg.B.32416 |
0.654 |
|
| 2016 |
Richard AC, Rovelet-Lecrux A, Delaby E, Charbonnier C, Thiruvahindrapuram B, Hatchwell E, Eis PS, Afenjar A, Dussardier BG, Scherer SW, Betancur C, Campion D. The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. DOI: 10.1002/ajmg.b.32416 |
0.591 |
|
| 2015 |
Mosca-Boidron AL, Gueneau L, Huguet G, Goldenberg A, Henry C, Gigot N, Pallesi-Pocachard E, Falace A, Duplomb L, Thevenon J, Duffourd Y, St-Onge J, Chambon P, Rivière JB, Thauvin-Robinet C, ... ... Campion D, et al. A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability. European Journal of Human Genetics : Ejhg. PMID 26395558 DOI: 10.1038/Ejhg.2015.211 |
0.375 |
|
| 2015 |
Nicolas G, Wallon D, Charbonnier C, Quenez O, Rousseau S, Richard AC, Rovelet-Lecrux A, Coutant S, Le Guennec K, Bacq D, Garnier JG, Olaso R, Boland A, Meyer V, Deleuze JF, ... ... Campion D, et al. Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons. European Journal of Human Genetics : Ejhg. PMID 26242991 DOI: 10.1038/Ejhg.2015.173 |
0.7 |
|
| 2015 |
Rovelet-Lecrux A, Charbonnier C, Wallon D, Nicolas G, Seaman MN, Pottier C, Breusegem SY, Mathur PP, Jenardhanan P, Le Guennec K, Mukadam AS, Quenez O, Coutant S, Rousseau S, Richard AC, ... ... Campion D, et al. De novo deleterious genetic variations target a biological network centered on Aβ peptide in early-onset Alzheimer disease. Molecular Psychiatry. PMID 26194182 DOI: 10.1038/Mp.2015.100 |
0.707 |
|
| 2015 |
Nicolas G, Charbonnier C, de Lemos RR, Richard AC, Guillin O, Wallon D, Legati A, Geschwind D, Coppola G, Frebourg T, Campion D, de Oliveira JR, Hannequin D. Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 26129893 DOI: 10.1002/Ajmg.B.32336 |
0.384 |
|
| 2015 |
Lambert JC, Grenier-Boley B, Bellenguez C, Pasquier F, Campion D, Dartigues JF, Berr C, Tzourio C, Amouyel P. PLD3 and sporadic Alzheimer's disease risk. Nature. 520: E1. PMID 25832408 DOI: 10.1038/Nature14036 |
0.347 |
|
| 2015 |
Nicolas G, Wallon D, Goupil C, Richard AC, Pottier C, Dorval V, Sarov-Rivière M, Riant F, Hervé D, Amouyel P, Guerchet M, Ndamba-Bandzouzi B, Mbelesso P, Dartigues JF, Lambert JC, ... ... Campion D, et al. Mutation in the 3'untranslated region of APP as a genetic determinant of cerebral amyloid angiopathy. European Journal of Human Genetics : Ejhg. PMID 25828868 DOI: 10.1038/Ejhg.2015.61 |
0.686 |
|
| 2015 |
Lemos RR, Ramos EM, Legati A, Nicolas G, Jenkinson EM, Livingston JH, Crow YJ, Campion D, Coppola G, Oliveira JR. Update and Mutational Analysis of SLC20A2: A Major Cause of Primary Familial Brain Calcification. Human Mutation. 36: 489-95. PMID 25726928 DOI: 10.1002/Humu.22778 |
0.389 |
|
| 2014 |
Guipponi M, Santoni FA, Setola V, Gehrig C, Rotharmel M, Cuenca M, Guillin O, Dikeos D, Georgantopoulos G, Papadimitriou G, Curtis L, Méary A, Schürhoff F, Jamain S, Avramopoulos D, ... ... Campion D, et al. Exome sequencing in 53 sporadic cases of schizophrenia identifies 18 putative candidate genes. Plos One. 9: e112745. PMID 25420024 DOI: 10.1371/Journal.Pone.0112745 |
0.397 |
|
| 2014 |
Escott-Price V, Bellenguez C, Wang LS, Choi SH, Harold D, Jones L, Holmans P, Gerrish A, Vedernikov A, Richards A, DeStefano AL, Lambert JC, Ibrahim-Verbaas CA, Naj AC, Sims R, ... ... Campion D, et al. Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. Plos One. 9: e94661. PMID 24922517 DOI: 10.1371/Journal.Pone.0094661 |
0.423 |
|
| 2014 |
Nicolas G, Richard AC, Pottier C, Verny C, Durif F, Roze E, Favrole P, Rudolf G, Anheim M, Tranchant C, Frebourg T, Campion D, Hannequin D. Overall mutational spectrum of SLC20A2, PDGFB and PDGFRB in idiopathic basal ganglia calcification. Neurogenetics. 15: 215-6. PMID 24770784 DOI: 10.1007/S10048-014-0404-2 |
0.318 |
|
| 2014 |
Nicolas G, Rovelet-Lecrux A, Pottier C, Martinaud O, Wallon D, Vernier L, Landemore G, Chapon F, Prieto-Morin C, Tournier-Lasserve E, Frébourg T, Campion D, Hannequin D. PDGFB partial deletion: a new, rare mechanism causing brain calcification with leukoencephalopathy. Journal of Molecular Neuroscience : Mn. 53: 171-5. PMID 24604296 DOI: 10.1007/S12031-014-0265-Z |
0.715 |
|
| 2014 |
Nicolas G, Jacquin A, Thauvin-Robinet C, Rovelet-Lecrux A, Rouaud O, Pottier C, Aubriot-Lorton MH, Rousseau S, Wallon D, Duvillard C, Béjot Y, Frébourg T, Giroud M, Campion D, Hannequin D. A de novo nonsense PDGFB mutation causing idiopathic basal ganglia calcification with laryngeal dystonia. European Journal of Human Genetics : Ejhg. 22: 1236-8. PMID 24518837 DOI: 10.1038/Ejhg.2014.9 |
0.676 |
|
| 2014 |
Clot F, Rovelet-Lecrux A, Lamari F, Noël S, Keren B, Camuzat A, Michon A, Jornea L, Laudier B, de Septenville A, Caroppo P, Campion D, Cazeneuve C, Brice A, LeGuern E, et al. Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration. Neurogenetics. 15: 95-100. PMID 24469240 DOI: 10.1007/S10048-014-0389-X |
0.678 |
|
| 2014 |
Wallon D, Rovelet-Lecrux A, Pasquier F, Le Ber I, Paquet C, Campion D, Hannequin D. Génétique de la maladie d’Alzheimer sporadique avant 50ans Revue Neurologique. 170: A196-A197. DOI: 10.1016/J.Neurol.2014.01.525 |
0.606 |
|
| 2013 |
Nicolas G, Pottier C, Charbonnier C, Guyant-Maréchal L, Le Ber I, Pariente J, Labauge P, Ayrignac X, Defebvre L, Maltête D, Martinaud O, Lefaucheur R, Guillin O, Wallon D, Chaumette B, ... ... Campion D, et al. Phenotypic spectrum of probable and genetically-confirmed idiopathic basal ganglia calcification. Brain : a Journal of Neurology. 136: 3395-407. PMID 24065723 DOI: 10.1093/Brain/Awt255 |
0.686 |
|
| 2013 |
Le Ber I, Camuzat A, Guerreiro R, Bouya-Ahmed K, Bras J, Nicolas G, Gabelle A, Didic M, De Septenville A, Millecamps S, Lenglet T, Latouche M, Kabashi E, Campion D, Hannequin D, et al. SQSTM1 mutations in French patients with frontotemporal dementia or frontotemporal dementia with amyotrophic lateral sclerosis. Jama Neurology. 70: 1403-10. PMID 24042580 DOI: 10.1001/Jamaneurol.2013.3849 |
0.395 |
|
| 2013 |
Keller A, Westenberger A, Sobrido MJ, GarcÃa-Murias M, Domingo A, Sears RL, Lemos RR, Ordoñez-Ugalde A, Nicolas G, da Cunha JE, Rushing EJ, Hugelshofer M, Wurnig MC, Kaech A, Reimann R, ... ... Campion D, et al. Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice. Nature Genetics. 45: 1077-82. PMID 23913003 DOI: 10.1038/Ng.2723 |
0.36 |
|
| 2013 |
Pierrot N, Tyteca D, D'auria L, Dewachter I, Gailly P, Hendrickx A, Tasiaux B, Haylani LE, Muls N, N'kuli F, Laquerrière A, Demoulin JB, Campion D, Brion JP, Courtoy PJ, et al. Amyloid precursor protein controls cholesterol turnover needed for neuronal activity. Embo Molecular Medicine. 5: 608-25. PMID 23554170 DOI: 10.1002/Emmm.201202215 |
0.311 |
|
| 2013 |
Chapuis J, Hansmannel F, Gistelinck M, Mounier A, Van Cauwenberghe C, Kolen KV, Geller F, Sottejeau Y, Harold D, Dourlen P, Grenier-Boley B, Kamatani Y, Delepine B, Demiautte F, Zelenika D, ... ... Campion D, et al. Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology. Molecular Psychiatry. 18: 1225-34. PMID 23399914 DOI: 10.1038/Mp.2013.1 |
0.441 |
|
| 2013 |
Pottier C, Wallon D, Rousseau S, Rovelet-Lecrux A, Richard AC, Rollin-Sillaire A, Frebourg T, Campion D, Hannequin D. TREM2 R47H variant as a risk factor for early-onset Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 35: 45-9. PMID 23380991 DOI: 10.3233/Jad-122311 |
0.714 |
|
| 2013 |
Huc-Chabrolle M, Charon C, Guilmatre A, Vourc'h P, Tripi G, Barthez MA, Sizaret E, Thepault RA, Le Gallic S, Hager J, Toutain A, Raynaud M, Andres C, Campion D, Laumonnier F, et al. Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families. Behavior Genetics. 43: 132-40. PMID 23307483 DOI: 10.1007/S10519-012-9575-5 |
0.382 |
|
| 2013 |
Nicolas G, Pottier C, Maltête D, Coutant S, Rovelet-Lecrux A, Legallic S, Rousseau S, Vaschalde Y, Guyant-Maréchal L, Augustin J, Martinaud O, Defebvre L, Krystkowiak P, Pariente J, Clanet M, ... ... Campion D, et al. Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification. Neurology. 80: 181-7. PMID 23255827 DOI: 10.1212/Wnl.0B013E31827Ccf34 |
0.678 |
|
| 2013 |
Saint-Aubert L, Payoux P, Hannequin D, Barbeau EJ, Campion D, Delisle MB, Tafani M, Viallard G, Péran P, Puel M, Chollet F, Demonet JF, Pariente J. MR, (18)F-FDG, and (18)F-AV45 PET correlate with AD PSEN1 original phenotype. Alzheimer Disease and Associated Disorders. 27: 91-4. PMID 22517194 DOI: 10.1097/Wad.0B013E318251D87C |
0.35 |
|
| 2013 |
Lambert JC, Grenier-Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram MA, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, ... ... Campion D, et al. Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease. Molecular Psychiatry. 18: 461-70. PMID 22430674 DOI: 10.1038/Mp.2012.14 |
0.398 |
|
| 2013 |
Lambert JC, Grenier-Boley B, Harold D, Zelenika D, Chouraki V, Kamatani Y, Sleegers K, Ikram MA, Hiltunen M, Reitz C, Mateo I, Feulner T, Bullido M, Galimberti D, Concari L, ... ... Campion D, et al. Erratum: Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease (Molecular Psychiatry (2013) 18 (521) DOI: 10.1038/mp.2012.75)) Molecular Psychiatry. 18. DOI: 10.1038/Mp.2012.75 |
0.386 |
|
| 2013 |
Buee-Scherrer V, Papegaey A, Deramecourt V, Lecourtois M, Lebert F, Campion D, Pasquier F, Sergeant N, Buee L. Frontotemporal lobar degeneration: Any link between tau and TDP-43? Alzheimers & Dementia. 9: 438. DOI: 10.1016/J.Jalz.2013.05.867 |
0.368 |
|
| 2012 |
Levinson DF, Shi J, Wang K, Oh S, Riley B, Pulver AE, Wildenauer DB, Laurent C, Mowry BJ, Gejman PV, Owen MJ, Kendler KS, Nestadt G, Schwab SG, Mallet J, ... ... Campion D, et al. Genome-wide association study of multiplex schizophrenia pedigrees. The American Journal of Psychiatry. 169: 963-73. PMID 22885689 DOI: 10.1176/Appi.Ajp.2012.11091423 |
0.333 |
|
| 2012 |
Rovelet-Lecrux A, Campion D. Copy number variations involving the microtubule-associated protein tau in human diseases. Biochemical Society Transactions. 40: 672-6. PMID 22817714 DOI: 10.1042/Bst20120045 |
0.722 |
|
| 2012 |
Wallon D, Rovelet-Lecrux A, Deramecourt V, Pariente J, Auriacombe S, Le Ber I, Schraen S, Pasquier F, Campion D, Hannequin D. Definite behavioral variant of frontotemporal dementia with C9ORF72 expansions despite positive Alzheimer's disease cerebrospinal fluid biomarkers. Journal of Alzheimer's Disease : Jad. 32: 19-22. PMID 22766732 DOI: 10.3233/Jad-2012-120877 |
0.693 |
|
| 2012 |
Tlili A, Hoischen A, Ripoll C, Benabou E, Badel A, Ronan A, Touraine R, Grattau Y, Stora S, van Bon B, de Vries B, Menten B, Bockaert N, Gecz J, Antonarakis SE, ... Campion D, et al. BDNF and DYRK1A are variable and inversely correlated in lymphoblastoid cell lines from Down syndrome patients. Molecular Neurobiology. 46: 297-303. PMID 22669612 DOI: 10.1007/S12035-012-8284-7 |
0.318 |
|
| 2012 |
Wallon D, Rousseau S, Rovelet-Lecrux A, Quillard-Muraine M, Guyant-Maréchal L, Martinaud O, Pariente J, Puel M, Rollin-Sillaire A, Pasquier F, Le Ber I, Sarazin M, Croisile B, Boutoleau-Bretonnière C, Thomas-Antérion C, ... ... Campion D, et al. The French series of autosomal dominant early onset Alzheimer's disease cases: mutation spectrum and cerebrospinal fluid biomarkers. Journal of Alzheimer's Disease : Jad. 30: 847-56. PMID 22475797 DOI: 10.3233/Jad-2012-120172 |
0.721 |
|
| 2012 |
Rovelet-Lecrux A, Legallic S, Wallon D, Flaman JM, Martinaud O, Bombois S, Rollin-Sillaire A, Michon A, Le Ber I, Pariente J, Puel M, Paquet C, Croisile B, Thomas-Antérion C, Vercelletto M, ... ... Campion D, et al. A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease. European Journal of Human Genetics : Ejhg. 20: 613-7. PMID 22166940 DOI: 10.1038/Ejhg.2011.225 |
0.74 |
|
| 2012 |
Saint-Aubert L, Planton M, Hannequin D, Albucher JF, Delisle MB, Payoux P, Hitzel A, Viallard G, Péran P, Campion D, Laquerrière A, Barbeau EJ, Puel M, Raposo N, Chollet F, et al. Amyloid imaging with AV45 ((18)F-florbetapir) in a cognitively normal AβPP duplication carrier. Journal of Alzheimer's Disease : Jad. 28: 877-83. PMID 22156048 DOI: 10.3233/Jad-2011-111598 |
0.41 |
|
| 2012 |
Miguel L, Avequin T, Delarue M, Feuillette S, Frébourg T, Campion D, Lecourtois M. Accumulation of insoluble forms of FUS protein correlates with toxicity in Drosophila. Neurobiology of Aging. 33: 1008.e1-15. PMID 22118902 DOI: 10.1016/J.Neurobiolaging.2011.10.008 |
0.782 |
|
| 2012 |
Le Ber I, Camuzat A, Guillot-Noel L, Guedj E, Hannequin D, Wargon I, Couratier P, Deramecourt V, Berger E, Viennet G, Pasquier F, Lacomblez Aurousseau L, Salachas F, Martinaud O, Golfier V, ... ... Campion D, et al. Frequency and Phenotypes Associated with C9ORF72 Repeat Expansion in French FTLD and FTLD-ALS Patients (S54.003) Neurology. 78: S54.003-S54.003. DOI: 10.1212/Wnl.78.1_Meetingabstracts.S54.003 |
0.374 |
|
| 2012 |
Wallon D, Pottier C, Rovelet-Lecrux A, Maltête D, Jurici S, Hannequin D, Campion D. Expression du gène APP au niveau des lymphocytes périphériques dans la maladie d’Alzheimer Revue Neurologique. 168: A11-A12. DOI: 10.1016/J.Neurol.2012.01.024 |
0.622 |
|
| 2012 |
Wallon D, Rovelet-Lecrux A, Rousseau S, Martinaud O, Pottier C, Rollin A, Pasquier F, Le Ber I, Dubois B, Pariente J, Paquet C, Croisile B, Thomas-Anterion C, Campion D, Hannequin D. P4-097: Alzheimer's disease with age of onset less than 50 years: Genetic determinisms in sporadic cases Alzheimer's & Dementia. 8: P666-P667. DOI: 10.1016/J.Jalz.2012.05.1799 |
0.685 |
|
| 2011 |
Jacquemont S, Reymond A, Zufferey F, Harewood L, Walters RG, Kutalik Z, Martinet D, Shen Y, Valsesia A, Beckmann ND, Thorleifsson G, Belfiore M, Bouquillon S, Campion D, de Leeuw N, et al. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature. 478: 97-102. PMID 21881559 DOI: 10.1038/Nature10406 |
0.318 |
|
| 2011 |
Genin E, Hannequin D, Wallon D, Sleegers K, Hiltunen M, Combarros O, Bullido MJ, Engelborghs S, De Deyn P, Berr C, Pasquier F, Dubois B, Tognoni G, Fiévet N, Brouwers N, ... ... Campion D, et al. APOE and Alzheimer disease: a major gene with semi-dominant inheritance. Molecular Psychiatry. 16: 903-7. PMID 21556001 DOI: 10.1038/Mp.2011.52 |
0.384 |
|
| 2011 |
Miguel L, Frébourg T, Campion D, Lecourtois M. Both cytoplasmic and nuclear accumulations of the protein are neurotoxic in Drosophila models of TDP-43 proteinopathies. Neurobiology of Disease. 41: 398-406. PMID 20951205 DOI: 10.1016/J.Nbd.2010.10.007 |
0.779 |
|
| 2011 |
Cousin E, Macé S, Rocher C, Dib C, Muzard G, Hannequin D, Pradier L, Deleuze JF, Génin E, Brice A, Campion D. No replication of genetic association between candidate polymorphisms and Alzheimer's disease. Neurobiology of Aging. 32: 1443-51. PMID 19889475 DOI: 10.1016/J.Neurobiolaging.2009.09.004 |
0.405 |
|
| 2011 |
Goumidi L, Flamant F, Lendon C, Galimberti D, Pasquier F, Scarpini E, Hannequin D, Campion D, Amouyel P, Lambert JC, Meirhaeghe A. Study of thyroid hormone receptor alpha gene polymorphisms on Alzheimer's disease. Neurobiology of Aging. 32: 624-30. PMID 19427062 DOI: 10.1016/J.Neurobiolaging.2009.04.007 |
0.406 |
|
| 2011 |
Wallon D, Rovelet-Lecrux A, Martinaud O, Legallic S, Pottier C, Bombois S, Mackowiak M, Pasquier F, Michon A, Leber I, Dubois B, Pariente J, Paquet C, Croisile B, Thomas-Anterion C, ... ... Campion D, et al. Genetics of early-onset Alzheimer disease in France Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.552 |
0.693 |
|
| 2011 |
Bombois S, Campion D, Hannequin D, Delmaire C, Lehéricy S, Wallon D, Cordonnier C, Paulin M, Gerardin E, Dubois B, Pasquier F. P1-064: How prevalent are vascular lesions among early-onset Alzheimer's patients? Alzheimer's & Dementia. 7: S130-S131. DOI: 10.1016/J.Jalz.2011.05.343 |
0.301 |
|
| 2011 |
Paulin M, Richard F, Campion D, Wallon D, Hannequin D, Pasquier F. Diagnostic delay, medical and social pathways of early-onset Alzheimer's disease patients Alzheimers & Dementia. 7. DOI: 10.1016/J.Jalz.2011.05.1788 |
0.319 |
|
| 2011 |
Miguel L, Frébourg T, Campion D, Lecourtois M. P3-030: Characterization in drosophila of TDP-43 physiopathological pathways Alzheimer's & Dementia. 7: S524-S524. DOI: 10.1016/J.Jalz.2011.05.1469 |
0.744 |
|
| 2010 |
Lambert JC, Sleegers K, González-Pérez A, Ingelsson M, Beecham GW, Hiltunen M, Combarros O, Bullido MJ, Brouwers N, Bettens K, Berr C, Pasquier F, Richard F, Dekosky ST, Hannequin D, ... ... Campion D, et al. The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. Journal of Alzheimer's Disease : Jad. 22: 247-55. PMID 20847397 DOI: 10.3233/Jad-2010-100933 |
0.319 |
|
| 2010 |
Rovelet-Lecrux A, Hannequin D, Guillin O, Legallic S, Jurici S, Wallon D, Frebourg T, Campion D. Frontotemporal dementia phenotype associated with MAPT gene duplication. Journal of Alzheimer's Disease : Jad. 21: 897-902. PMID 20634582 DOI: 10.3233/Jad-2010-100441 |
0.701 |
|
| 2010 |
Guilmatre A, Legallic S, Steel G, Willis A, Di Rosa G, Goldenberg A, Drouin-Garraud V, Guet A, Mignot C, Des Portes V, Valayannopoulos V, Van Maldergem L, Hoffman JD, Izzi C, Espil-Taris C, ... ... Campion D, et al. Type I hyperprolinemia: genotype/phenotype correlations. Human Mutation. 31: 961-5. PMID 20524212 DOI: 10.1002/Humu.21296 |
0.339 |
|
| 2010 |
Seshadri S, Fitzpatrick AL, Ikram MA, DeStefano AL, Gudnason V, Boada M, Bis JC, Smith AV, Carassquillo MM, Lambert JC, Harold D, Schrijvers EM, Ramirez-Lorca R, Debette S, Longstreth WT, ... ... Campion D, et al. Genome-wide analysis of genetic loci associated with Alzheimer disease. Jama. 303: 1832-40. PMID 20460622 DOI: 10.1001/Jama.2010.574 |
0.396 |
|
| 2010 |
Feuillette S, Deramecourt V, Laquerriere A, Duyckaerts C, Delisle MB, Maurage CA, Blum D, Buée L, Frébourg T, Campion D, Lecourtois M. Filamin-A and Myosin VI colocalize with fibrillary Tau protein in Alzheimer's disease and FTDP-17 brains. Brain Research. 1345: 182-9. PMID 20460118 DOI: 10.1016/J.Brainres.2010.05.007 |
0.803 |
|
| 2010 |
Lambert JC, Grenier-Boley B, Chouraki V, Heath S, Zelenika D, Fievet N, Hannequin D, Pasquier F, Hanon O, Brice A, Epelbaum J, Berr C, Dartigues JF, Tzourio C, Campion D, et al. Implication of the immune system in Alzheimer's disease: evidence from genome-wide pathway analysis. Journal of Alzheimer's Disease : Jad. 20: 1107-18. PMID 20413860 DOI: 10.3233/Jad-2010-100018 |
0.407 |
|
| 2010 |
Laumet G, Chouraki V, Grenier-Boley B, Legry V, Heath S, Zelenika D, Fievet N, Hannequin D, Delepine M, Pasquier F, Hanon O, Brice A, Epelbaum J, Berr C, Dartigues JF, ... ... Campion D, et al. Systematic analysis of candidate genes for Alzheimer's disease in a French, genome-wide association study. Journal of Alzheimer's Disease : Jad. 20: 1181-8. PMID 20413850 DOI: 10.3233/JAD-2010-100126 |
0.306 |
|
| 2010 |
Feuillette S, Miguel L, Frébourg T, Campion D, Lecourtois M. Drosophila models of human tauopathies indicate that Tau protein toxicity in vivo is mediated by soluble cytosolic phosphorylated forms of the protein. Journal of Neurochemistry. 113: 895-903. PMID 20193038 DOI: 10.1111/J.1471-4159.2010.06663.X |
0.793 |
|
| 2010 |
Laumet G, Petitprez V, Sillaire A, Ayral AM, Hansmannel F, Chapuis J, Hannequin D, Pasquier F, Scarpini E, Galimberti D, Lendon C, Campion D, Amouyel P, Lambert JC. A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease. Neuroscience Letters. 468: 1-2. PMID 19837132 DOI: 10.1016/J.Neulet.2009.10.040 |
0.439 |
|
| 2009 |
Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, ... ... Campion D, et al. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease. Neurology. 72: 1669-76. PMID 19433740 DOI: 10.1212/Wnl.0B013E3181A55F1C |
0.377 |
|
| 2009 |
Benajiba L, Le Ber I, Camuzat A, Lacoste M, Thomas-Anterion C, Couratier P, Legallic S, Salachas F, Hannequin D, Decousus M, Lacomblez L, Guedj E, Golfier V, Camu W, Dubois B, ... Campion D, et al. TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration. Annals of Neurology. 65: 470-3. PMID 19350673 DOI: 10.1002/Ana.21612 |
0.445 |
|
| 2009 |
Rovelet-Lecrux A, Lecourtois M, Thomas-Anterion C, Le Ber I, Brice A, Frebourg T, Hannequin D, Campion D. Partial deletion of the MAPT gene: a novel mechanism of FTDP-17. Human Mutation. 30: E591-602. PMID 19263483 DOI: 10.1002/Humu.20979 |
0.691 |
|
| 2009 |
Guyant-Maréchal L, Campion D, Hannequin D. [Alzheimer disease: autosomal dominant forms]. Revue Neurologique. 165: 223-31. PMID 19081588 DOI: 10.1016/j.neurol.2008.10.019 |
0.336 |
|
| 2009 |
Hansmannel F, Lendon C, Pasquier F, Dumont J, Hannequin D, Chapuis J, Laumet G, Ayral AM, Galimberti D, Scarpini E, Campion D, Amouyel P, Lambert JC. Is the ornithine transcarbamylase gene a genetic determinant of Alzheimer's disease? Neuroscience Letters. 449: 76-80. PMID 18983895 DOI: 10.1016/j.neulet.2008.10.081 |
0.3 |
|
| 2009 |
Legallic S, Bou J, Haouzir S, Allio G, Demily C, Petit M, Frebourg T, Thibaut F, Campion D. No pathogenic rearrangement within the DISC 1 gene in psychosis. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 150: 148-50. PMID 18395819 DOI: 10.1002/Ajmg.B.30753 |
0.63 |
|
| 2009 |
Feuillette S, Deramecourt V, Laquerrière A, Blard O, Duyckaerts C, Delisle M, Maurage C, Frebourg T, Campion D, Lecourtois M. O1-6 Identification par crible génétique dans la drosophile de modulateurs de la neurotoxicité de la protéine Tau et caractérisation neuropathologique de leurs homologues humains Revue Neurologique. 165: 40. DOI: 10.1016/S0035-3787(09)72589-5 |
0.753 |
|
| 2009 |
Wallon D, Jurici S, Guyant-Maréchal L, Martinaud O, Laquerrière A, Rovelet-Lecrux A, Legallic S, Martin C, Bou J, Duyckaerts C, Le Ber I, Dubois B, Pasquier F, Hannequin D, Campion D. O1-1 Etat actuel des investigations dans les formes monogéniques de maladie d’Alzheimer du sujet jeune Revue Neurologique. 165: 37. DOI: 10.1016/S0035-3787(09)72584-6 |
0.649 |
|
| 2009 |
Laumet G, Petitprez V, Ayral A, Hansmanel F, Chapuis J, Hannequin D, Pasquier F, Galimberti D, Scarpini E, Lendon C, Campion D, Amouyel P, Lambert J. Association study of the ADAM12 and SH3MD1 genes with the risk of developing Alzheimer's disease Alzheimers & Dementia. 5. DOI: 10.1016/J.Jalz.2009.04.775 |
0.382 |
|
| 2009 |
Hansmannel F, Mann D, Lendon C, Hauw JJ, Laumet G, Ayral AM, Chapuis J, Hannequin D, DeKosky S, Pasquier F, Berr C, Galimberti D, Scarpini E, Kamboh I, Campion D, et al. Urea cycle and Alzheimer's disease Alzheimers & Dementia. 5: 461. DOI: 10.1016/J.Jalz.2009.04.769 |
0.344 |
|
| 2008 |
Guyant-Marechal I, Berger E, Laquerrière A, Rovelet-Lecrux A, Viennet G, Frebourg T, Rumbach L, Campion D, Hannequin D. Intrafamilial diversity of phenotype associated with app duplication. Neurology. 71: 1925-6. PMID 19047566 DOI: 10.1212/01.Wnl.0000339400.64213.56 |
0.7 |
|
| 2008 |
Dreses-Werringloer U, Lambert JC, Vingtdeux V, Zhao H, Vais H, Siebert A, Jain A, Koppel J, Rovelet-Lecrux A, Hannequin D, Pasquier F, Galimberti D, Scarpini E, Mann D, Lendon C, ... Campion D, et al. A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk. Cell. 133: 1149-61. PMID 18585350 DOI: 10.1016/J.Cell.2008.05.048 |
0.699 |
|
| 2008 |
Chapuis J, Moisan F, Mellick G, Elbaz A, Silburn P, Pasquier F, Hannequin D, Lendon C, Campion D, Amouyel P, Lambert JC. Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease. Human Molecular Genetics. 17: 2863-7. PMID 18579580 DOI: 10.1093/Hmg/Ddn183 |
0.385 |
|
| 2008 |
Rovelet-Lecrux A, Deramecourt V, Legallic S, Maurage CA, Le Ber I, Brice A, Lambert JC, Frébourg T, Hannequin D, Pasquier F, Campion D. Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease. Neurobiology of Disease. 31: 41-5. PMID 18479928 DOI: 10.1016/J.Nbd.2008.03.004 |
0.714 |
|
| 2008 |
Chapuis J, Hannequin D, Pasquier F, Bentham P, Brice A, Leber I, Frebourg T, Deleuze JF, Cousin E, Thaker U, Amouyel P, Mann D, Lendon C, Campion D, Lambert JC. Association study of the GAB2 gene with the risk of developing Alzheimer's disease. Neurobiology of Disease. 30: 103-6. PMID 18272374 DOI: 10.1016/J.Nbd.2007.12.006 |
0.415 |
|
| 2008 |
Le Ber I, Camuzat A, Hannequin D, Pasquier F, Guedj E, Rovelet-Lecrux A, Hahn-Barma V, van der Zee J, Clot F, Bakchine S, Puel M, Ghanim M, Lacomblez L, Mikol J, Deramecourt V, ... ... Campion D, et al. Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study. Brain : a Journal of Neurology. 131: 732-46. PMID 18245784 DOI: 10.1093/Brain/Awn012 |
0.719 |
|
| 2008 |
Di Rosa G, Pustorino G, Spano M, Campion D, Calabrò M, Aguennouz M, Caccamo D, Legallic S, Sgro DL, Bonsignore M, Tortorella G. Type I hyperprolinemia and proline dehydrogenase (PRODH) mutations in four Italian children with epilepsy and mental retardation. Psychiatric Genetics. 18: 40-2. PMID 18197084 DOI: 10.1097/Ypg.0B013E3282F08A3D |
0.34 |
|
| 2008 |
Campagne F, Lambert JC, Dreses-Werringloer U, Vingtdeux V, Lendon C, Campion D, Amouyel P, Lee AT, Gregersen PK, Davies P, Marambaud P. Response: CALHM1 Association with Alzheimer's Disease Risk Cell. 135: 994-996. DOI: 10.1016/J.Cell.2008.11.031 |
0.345 |
|
| 2007 |
Anheim M, Hannequin D, Boulay C, Martin C, Campion D, Tranchant C. Ataxic variant of Alzheimer's disease caused by Pro117Ala PSEN1 mutation. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 1414-5. PMID 18024701 DOI: 10.1136/Jnnp.2007.123026 |
0.464 |
|
| 2007 |
Demily C, Legallic S, Bou J, Houy-Durand E, Van Amelsvoort T, Zinkstok J, Manouvrier-Hanue S, Vogels A, Drouin-Garraud V, Philip N, Philippe A, Héron D, Sarda P, Petit M, Thibaut F, ... ... Campion D, et al. ZDHHC8 single nucleotide polymorphism rs175174 is not associated with psychiatric features of the 22q11 deletion syndrome or schizophrenia. Psychiatric Genetics. 17: 311-2. PMID 17728672 DOI: 10.1097/Ypg.0B013E328133F369 |
0.599 |
|
| 2007 |
Rovelet-Lecrux A, Frebourg T, Tuominen H, Majamaa K, Campion D, Remes AM. APP locus duplication in a Finnish family with dementia and intracerebral haemorrhage. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 1158-9. PMID 17442758 DOI: 10.1136/Jnnp.2006.113514 |
0.742 |
|
| 2007 |
Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, Laquerrière A, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas-Antérion C, et al. Progranulin null mutations in both sporadic and familial frontotemporal dementia. Human Mutation. 28: 846-55. PMID 17436289 DOI: 10.1002/Humu.20520 |
0.412 |
|
| 2007 |
Afenjar A, Moutard ML, Doummar D, Guët A, Rabier D, Vermersch AI, Mignot C, Burglen L, Heron D, Thioulouse E, de Villemeur TB, Campion D, Rodriguez D. Early neurological phenotype in 4 children with biallelic PRODH mutations. Brain & Development. 29: 547-52. PMID 17412540 DOI: 10.1016/J.Braindev.2007.01.008 |
0.377 |
|
| 2007 |
van der Zee J, Le Ber I, Maurer-Stroh S, Engelborghs S, Gijselinck I, Camuzat A, Brouwers N, Vandenberghe R, Sleegers K, Hannequin D, Dermaut B, Schymkowitz J, Campion D, Santens P, Martin JJ, et al. Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia. Human Mutation. 28: 416. PMID 17345602 DOI: 10.1002/Humu.9484 |
0.401 |
|
| 2007 |
Guyant-Maréchal L, Rovelet-Lecrux A, Goumidi L, Cousin E, Hannequin D, Raux G, Penet C, Ricard S, Macé S, Amouyel P, Deleuze JF, Frebourg T, Brice A, Lambert JC, Campion D. Variations in the APP gene promoter region and risk of Alzheimer disease. Neurology. 68: 684-7. PMID 17325276 DOI: 10.1212/01.Wnl.0000255938.33739.46 |
0.813 |
|
| 2007 |
Blard O, Feuillette S, Bou J, Chaumette B, Frébourg T, Campion D, Lecourtois M. Cytoskeleton proteins are modulators of mutant tau-induced neurodegeneration in Drosophila. Human Molecular Genetics. 16: 555-66. PMID 17309878 DOI: 10.1093/Hmg/Ddm011 |
0.791 |
|
| 2007 |
Raux G, Bumsel E, Hecketsweiler B, van Amelsvoort T, Zinkstok J, Manouvrier-Hanu S, Fantini C, Brévière GM, Di Rosa G, Pustorino G, Vogels A, Swillen A, Legallic S, Bou J, Opolczynski G, ... ... Campion D, et al. Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome. Human Molecular Genetics. 16: 83-91. PMID 17135275 DOI: 10.1093/Hmg/Ddl443 |
0.789 |
|
| 2006 |
Cabrejo L, Guyant-Maréchal L, Laquerrière A, Vercelletto M, De la Fournière F, Thomas-Antérion C, Verny C, Letournel F, Pasquier F, Vital A, Checler F, Frebourg T, Campion D, Hannequin D. Phenotype associated with APP duplication in five families. Brain : a Journal of Neurology. 129: 2966-76. PMID 16959815 DOI: 10.1093/Brain/Awl237 |
0.417 |
|
| 2006 |
Dumanchin C, Tournier I, Martin C, Didic M, Belliard S, Carlander B, Rouhart F, Duyckaerts C, Pellissier JF, Latouche JB, Hannequin D, Frebourg T, Tosi M, Campion D. Biological effects of four PSEN1 gene mutations causing Alzheimer disease with spastic paraparesis and cotton wool plaques. Human Mutation. 27: 1063. PMID 16941492 DOI: 10.1002/Humu.9458 |
0.392 |
|
| 2006 |
Blard O, Frébourg T, Campion D, Lecourtois M. Inhibition of proteasome and shaggy/glycogen synthase kinase-3β kinase prevents clearance of phosphorylated tau in Drosophila Journal of Neuroscience Research. 84: 1107-1115. PMID 16878320 DOI: 10.1002/Jnr.21006 |
0.358 |
|
| 2006 |
Guyant-Maréchal L, Laquerrière A, Duyckaerts C, Dumanchin C, Bou J, Dugny F, Le Ber I, Frébourg T, Hannequin D, Campion D. Valosin-containing protein gene mutations: clinical and neuropathologic features. Neurology. 67: 644-51. PMID 16790606 DOI: 10.1212/01.Wnl.0000225184.14578.D3 |
0.422 |
|
| 2006 |
Jacquet H, Rapoport JL, Hecketsweiler B, Bobb A, Thibaut F, Frébourg T, Campion D. Hyperprolinemia is not associated with childhood onset schizophrenia. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 192. PMID 16389584 DOI: 10.1002/Ajmg.B.30263 |
0.32 |
|
| 2006 |
Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerrière A, Vital A, Dumanchin C, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, Campion D. APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy. Nature Genetics. 38: 24-6. PMID 16369530 DOI: 10.1038/Ng1718 |
0.792 |
|
| 2005 |
Guyant-Maréchal L, Verrips A, Girard C, Wevers RA, Zijlstra F, Sistermans E, Vera P, Campion D, Hannequin D. Unusual cerebrotendinous xanthomatosis with fronto-temporal dementia phenotype. American Journal of Medical Genetics. Part A. 139: 114-7. PMID 16278884 DOI: 10.1002/Ajmg.A.30797 |
0.375 |
|
| 2005 |
Raux G, Guyant-Maréchal L, Martin C, Bou J, Penet C, Brice A, Hannequin D, Frebourg T, Campion D. Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: An update Journal of Medical Genetics. 42: 793-795. PMID 16033913 DOI: 10.1136/Jmg.2005.033456 |
0.779 |
|
| 2005 |
Martinaud O, Laquerrière A, Guyant-Maréchal L, Ahtoy P, Vera P, Sergeant N, Camuzat A, Bourgeois P, Hauw JJ, Campion D, Hannequin D. Frontotemporal dementia, motor neuron disease and tauopathy: clinical and neuropathological study in a family. Acta Neuropathologica. 110: 84-92. PMID 15965697 DOI: 10.1007/S00401-005-1028-2 |
0.371 |
|
| 2005 |
Feuillette S, Blard O, Lecourtois M, Frébourg T, Campion D, Dumanchin C. Tau is not normally degraded by the proteasome Journal of Neuroscience Research. 80: 400-405. PMID 15795929 DOI: 10.1002/Jnr.20414 |
0.806 |
|
| 2005 |
Macé S, Cousin E, Ricard S, Génin E, Spanakis E, Lafargue-Soubigou C, Génin B, Fournel R, Roche S, Haussy G, Massey F, Soubigou S, Bréfort G, Benoit P, Brice A, ... Campion D, et al. ABCA2 is a strong genetic risk factor for early-onset Alzheimer's disease Neurobiology of Disease. 18: 119-125. PMID 15649702 DOI: 10.1016/J.Nbd.2004.09.011 |
0.402 |
|
| 2005 |
Jacquet H, Demily C, Houy E, Hecketsweiler B, Bou J, Raux G, Lerond J, Allio G, Haouzir S, Tillaux A, Bellegou C, Fouldrin G, Delamillieure P, Ménard JF, Dollfus S, ... ... Campion D, et al. Hyperprolinemia is a risk factor for schizoaffective disorder. Molecular Psychiatry. 10: 479-85. PMID 15494707 DOI: 10.1038/Sj.Mp.4001597 |
0.785 |
|
| 2004 |
Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, et al. A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24. Brain : a Journal of Neurology. 127: 1979-92. PMID 15215218 DOI: 10.1093/Brain/Awh216 |
0.754 |
|
| 2004 |
Houy E, Raux G, Thibaut F, Belmont A, Demily C, Allio G, Haouzir S, Fouldrin G, Petit M, Frebourg T, Campion D. The promoter -194 C polymorphism of the nicotinic alpha 7 receptor gene has a protective effect against the P50 sensory gating deficit. Molecular Psychiatry. 9: 320-2. PMID 14569275 DOI: 10.1038/Sj.Mp.4001443 |
0.759 |
|
| 2004 |
Dumanchin C, Feuillette S, Frebourg T, Campion D. P3-239 Tau is not degraded in vitro in SH5Y-SY human cells by the 26S proteasome under physiological conditions Neurobiology of Aging. 25: S423. DOI: 10.1016/S0197-4580(04)81389-7 |
0.76 |
|
| 2003 |
Cousin E, Hannequin D, Macé S, Dubois B, Ricard S, Génin E, Brun C, Chansac C, Pradier L, Frebourg T, Brice A, Campion D, Deleuze JF. No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease Neuroscience Letters. 353: 153-155. PMID 14664923 DOI: 10.1016/S0304-3940(03)01105-4 |
0.433 |
|
| 2003 |
Portet F, Dauvilliers Y, Campion D, Raux G, Hauw JJ, Lyon-Caen O, Camu W, Touchon J. Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu). Neurology. 61: 1136-7. PMID 14581682 DOI: 10.1212/01.Wnl.0000086811.39675.79 |
0.77 |
|
| 2003 |
Erickson RP, Skinner S, Jacquet H, Campion D, Buckley PG, Mantripragada KK, Dumanski JP. Does chromosome 22 have anything to do with sex determination: further studies on a 46,XX,22q11.2 del male. American Journal of Medical Genetics. Part A. 123: 64-7. PMID 14556248 DOI: 10.1002/Ajmg.A.20489 |
0.313 |
|
| 2003 |
Maréchal L, Campion D, Hannequin D. Familial alzheimer disease | Les formes familiales de la maladie d'alzheimer Presse Medicale. 32: 756-763. PMID 12856536 |
0.37 |
|
| 2003 |
Cousin E, Hannequin D, Ricard S, Macé S, Génin E, Chansac C, Brice A, Dubois B, Frebourg T, Mercken L, Benavides J, Pradier L, Campion D, Deleuze JF. A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism Neuroscience Letters. 342: 5-8. PMID 12727304 DOI: 10.1016/S0304-3940(03)00225-8 |
0.442 |
|
| 2003 |
Maréchal L, Raux G, Dumanchin C, Lefebvre G, Deslandre E, Girard C, Campion D, Parain D, Frebourg T, Hannequin D. Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation American Journal of Medical Genetics - Neuropsychiatric Genetics. 119: 114-117. PMID 12707948 DOI: 10.1002/Ajmg.B.10062 |
0.747 |
|
| 2003 |
Jacquet H, Berthelot J, Bonnemains C, Simard G, Saugier-Veber P, Raux G, Campion D, Bonneau D, Frebourg T. The severe form of type I hyperprolinaemia results from homozygous inactivation of the PRODH gene Journal of Medical Genetics. 40: e7. PMID 12525555 DOI: 10.1136/Jmg.40.1.E7 |
0.725 |
|
| 2002 |
Verpillat P, Ricard S, Hannequin D, Dubois B, Bou J, Camuzat A, Pradier L, Frebourg T, Brice A, Clerget-Darpoux F, Deleuze JF, Campion D, Belliard S, Didic M, Golfier V, et al. Is the saitohin gene involved in neurodegenerative diseases? Annals of Neurology. 52: 829-832. PMID 12447938 DOI: 10.1002/Ana.10384 |
0.439 |
|
| 2002 |
Raux G, Bonnet-Brilhault F, Louchart S, Houy E, Gantier R, Levillain D, Allio G, Haouzir S, Petit M, Martinez M, Frebourg T, Thibaut F, Campion D. The -2 bp deletion in exon 6 of the 'alpha 7-like' nicotinic receptor subunit gene is a risk factor for the P50 sensory gating deficit Molecular Psychiatry. 7: 1006-1011. PMID 12399955 DOI: 10.1038/Sj.Mp.4001140 |
0.729 |
|
| 2002 |
Jacquet H, Raux G, Thibaut F, Hecketsweiler B, Houy E, Demilly C, Haouzir S, Allio G, Fouldrin G, Drouin V, Bou J, Petit M, Campion D, Frébourg T. PRODH mutations and hyperprolinemia in a subset of schizophrenic patients Human Molecular Genetics. 11: 2243-2249. PMID 12217952 DOI: 10.1093/Hmg/11.19.2243 |
0.747 |
|
| 2002 |
Boussaha M, Hannequin D, Verpillat P, Brice A, Frebourg T, Campion D. Polymorphisms of insulin degrading enzyme gene are not associated with Alzheimer's disease Neuroscience Letters. 329: 121-123. PMID 12161276 DOI: 10.1016/S0304-3940(02)00586-4 |
0.413 |
|
| 2002 |
Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Lacomblez L, Moreaud O, Golfier V, Campion D, Brice A, Clerget-Darpoux F. Apolipoprotein E gene in frontotemporal dementia: An association study and meta-analysis European Journal of Human Genetics. 10: 399-405. PMID 12107813 DOI: 10.1038/Sj.Ejhg.5200820 |
0.378 |
|
| 2002 |
Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Michel BF, Lacomblez L, Moreaud O, Sellal F, Golfier V, Campion D, Clerget-Darpoux F, et al. Association between the extended tau haplotype and frontotemporal dementia Archives of Neurology. 59: 935-939. PMID 12056929 DOI: 10.1001/Archneur.59.6.935 |
0.478 |
|
| 2002 |
Jacquemont ML, Campion D, Hahn V, Tallaksen C, Frebourg T, Brice A, Durr A. Spastic paraparesis and atypical dementia caused by PSEN1 mutation (P264L), responsible for Alzheimer's disease Journal of Medical Genetics. 39: E2. PMID 11836371 DOI: 10.1136/Jmg.39.2.E2 |
0.455 |
|
| 2001 |
Verpillat P, Bouley S, Campion D, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Antérion C, Agid Y, Brice A, Clerget-Darpoux F. Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population. European Journal of Human Genetics : Ejhg. 9: 464-8. PMID 11436129 DOI: 10.1038/Sj.Ejhg.5200644 |
0.403 |
|
| 2001 |
De Chaldée M, Corbex M, Campion D, Jay M, Samolyk D, Petit M, Thibaut F, Laurent C, Mallet J. No evidence for linkage between COMT and schizophrenia in a French population Psychiatry Research. 102: 87-90. PMID 11368843 DOI: 10.1016/S0165-1781(01)00237-2 |
0.309 |
|
| 2000 |
Raux G, Gantier R, Thomas-Anterion C, Boulliat J, Verpillat P, Hannequin D, Brice A, Frebourg T, Campion D. Dementia with prominent frontotemporal features associated with L113P presenilin 1 mutation Neurology. 55: 1577-1578. PMID 11094121 DOI: 10.1212/Wnl.55.10.1577 |
0.738 |
|
| 2000 |
Zurutuza L, Verpillat P, Raux G, Hannequin D, Puel M, Belliard S, Michon A, Pothin Y, Camuzat A, Penet C, Martin C, Brice A, Campion D, Clerget-Darpoux F, Frebourg T. APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population European Journal of Human Genetics. 8: 713-716. PMID 10980578 DOI: 10.1038/Sj.Ejhg.5200513 |
0.739 |
|
| 2000 |
Lopez-Perez E, Dumanchin C, Czech C, Campion D, Goud B, Pradier L, Frebourg T, Checler F. Overexpression of Rab11 or constitutively active Rab11 does not affect sAPPα and Aβ secretions by wild-type and Swedish mutated βAPP-expressing HEK293 cells Biochemical and Biophysical Research Communications. 275: 910-915. PMID 10973821 DOI: 10.1006/Bbrc.2000.3404 |
0.408 |
|
| 2000 |
Raux G, Gantier R, Martin C, Pothin Y, Brice A, Frebourg T, Campion D. A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease. Human Mutation. 16: 95. PMID 10874324 DOI: 10.1002/1098-1004(200007)16:1<95::Aid-Humu28>3.0.Co;2-H |
0.757 |
|
| 2000 |
Gantier R, Gilbert D, Dumanchin C, Campion D, Davoust D, Toma F, Frébourg T. The pathogenic L392V mutation of presenilin 1 decreases the affinity to glycogen synthase kinase-3 beta. Neuroscience Letters. 283: 217-20. PMID 10754226 DOI: 10.1016/S0304-3940(00)00949-6 |
0.399 |
|
| 2000 |
Checler F, Ancolio K, Dumanchin C, Fouques O, Campion D, Frebourg T. Phenotypic alterations triggerred by a novel mutation responsible for early onset Alzheimer's disease: A study on βAPP maturation and apoptotic response Neurobiology of Aging. 21: 23. DOI: 10.1016/S0197-4580(00)82782-7 |
0.39 |
|
| 2000 |
Verpillat P, Bouley S, Hannequin D, Belliard S, Puel M, Campion D, Clerget-Darpoux F, Brice A. Genetic association between Alzheimer's disease and the low density lipoprotein receptor-related protein gene in the French population Neurobiology of Aging. 21: 64. DOI: 10.1016/S0197-4580(00)82510-5 |
0.359 |
|
| 2000 |
Verpillat P, Bouley S, Hannequin D, Belliard S, Puel M, Campion D, Clerget-Darpoux F, Brice A. Genetic association between alpha 2-macroglobulin gene and Alzheimer's disease in the French population Neurobiology of Aging. 21: 173. DOI: 10.1016/S0197-4580(00)82117-X |
0.352 |
|
| 2000 |
Verpillat P, Bouley S, Hannequin D, Belliard S, Puel M, Thomas-Anterion C, Dubois B, Agid Y, Campion D, Clerget-Darpoux F, Brice A. α2-Macroglobulin gene and Alzheimer's disease: Confirmation of association by haplotypes analyses Annals of Neurology. 48: 400-402. DOI: 10.1002/1531-8249(200009)48:3<400::Aid-Ana22>3.0.Co;2-L |
0.372 |
|
| 1999 |
Gantier R, Dumanchin C, Campion D, Loutelier C, Lange C, Gagnon J, Davoust D, Frébourg T, Toma F. The L392V mutation of presenilin 1 associated with autosomal dominant early-onset Alzheimer's disease alters the secondary structure of the hydrophilic loop. Neuroreport. 10: 3071-3074. PMID 10549825 DOI: 10.1097/00001756-199909290-00036 |
0.398 |
|
| 1999 |
de Chaldée M, Laurent C, Thibaut F, Martinez M, Samolyk D, Petit M, Campion D, Mallet J. Linkage disequilibrium on the COMT gene in French schizophrenics and controls. American Journal of Medical Genetics. 88: 452-7. PMID 10490696 DOI: 10.1002/(Sici)1096-8628(19991015)88:5<452::Aid-Ajmg2>3.0.Co;2-0 |
0.31 |
|
| 1999 |
Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Anterion C, Michon A, Martin C, Charbonnier F, Raux G, Camuzat A, Penet C, Mesnage V, Martinez M, et al. Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum American Journal of Human Genetics. 65: 664-670. PMID 10441572 DOI: 10.1086/302553 |
0.761 |
|
| 1999 |
Dumanchin C, Czech C, Campion D, Cuif MH, Poyot T, Martin C, Charbonnier F, Goud B, Pradier L, Frebourg T. Presenilins interact with Rab11, a small GTPase involved in the regulation of vesicular transport. Human Molecular Genetics. 8: 1263-9. PMID 10369872 DOI: 10.1093/Hmg/8.7.1263 |
0.349 |
|
| 1999 |
Ancolio K, Dumanchin C, Barelli H, Warter JM, Brice A, Campion D, Frébourg T, Checler F. Unusual phenotypic alteration of beta amyloid precursor protein (betaAPP) maturation by a new Val-715 --> Met betaAPP-770 mutation responsible for probable early-onset Alzheimer's disease. Proceedings of the National Academy of Sciences of the United States of America. 96: 4119-24. PMID 10097173 DOI: 10.1073/Pnas.96.7.4119 |
0.423 |
|
| 1998 |
Dumanchin C, Camuzat A, Campion D, Verpillat P, Hannequin D, Dubois B, Saugier-Veber P, Martin C, Penet C, Charbonnier F, Agid Y, Frebourg T, Brice A. Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism. Human Molecular Genetics. 7: 1825-9. PMID 9736786 DOI: 10.1093/Hmg/7.11.1825 |
0.475 |
|
| 1998 |
Dumanchin C, Brice A, Campion D, Hannequin D, Martin C, Moreau V, Agid Y, Martinez M, Clerget-Darpoux F, Frebourg T. De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group. Journal of Medical Genetics. 35: 672-3. PMID 9719376 DOI: 10.1136/Jmg.35.8.672 |
0.465 |
|
| 1998 |
Vallada H, Curtis D, Sham P, Kunugi H, Zhao J, Murray R, McGuffin P, Nanko S, Owen M, Gill M, Collier D, Antonarakis S, Housman D, Kazazian H, Nestadt G, ... ... Campion D, et al. A transmission disequilibrium and linkage analysis of D22S278 marker alleles in 574 families: further support for a susceptibility locus for schizophrenia at 22q12 Schizophrenia Research. 32: 115-121. PMID 9713907 DOI: 10.1016/S0920-9964(98)00048-6 |
0.329 |
|
| 1998 |
Laurent C, Zander C, Thibaut F, Bonnet-Brilhault F, Chavand O, Jay M, Samolyk D, Petit M, Martinez M, Campion D, Néri C, Mallet J, Cann H. Anticipation in schizophrenia: no evidence of expanded CAG/CTG repeat sequences in French families and sporadic cases. American Journal of Medical Genetics. 81: 342-6. PMID 9674982 DOI: 10.1002/(Sici)1096-8628(19980710)81:4<342::Aid-Ajmg12>3.0.Co;2-L |
0.322 |
|
| 1998 |
Martinez M, Campion D, Brice A, Hannequin D, Dubois B, Didierjean O, Michon A, Thomas-Anterion C, Puel M, Frebourg T, Agid Y, Clerget-Darpoux F. Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease. Archives of Neurology. 55: 810-6. PMID 9626772 DOI: 10.1001/Archneur.55.6.810 |
0.401 |
|
| 1998 |
Thibaut F, Coron B, Hannequin D, Segard L, Martin C, Dollfus S, Campion D, Frebourg T, Petit M. No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients Schizophrenia Research. 30: 149-153. PMID 9549778 DOI: 10.1016/S0920-9964(97)00147-3 |
0.304 |
|
| 1997 |
Malafosse A, Leboyer M, d'Amato T, Amadéo S, Abbar M, Campion D, Canseil O, Castelnau D, Gheysen F, Granger B, Henrikson B, Poirier MF, Sabaté O, Samolyk D, Feingold J, et al. Manic depressive illness and tyrosine hydroxylase gene: linkage heterogeneity and association. Neurobiology of Disease. 4: 337-49. PMID 9440122 DOI: 10.1006/Nbdi.1997.0149 |
0.333 |
|
| 1997 |
Laurent C, Thibaut F, Ravassard P, Campion D, Samolyk D, Lafargue C, Petit M, Martinez M, Mallet J. Detection of two new polymorphic sites in the human interleukin-1 beta gene: lack of association with schizophrenia in a French population. Psychiatric Genetics. 7: 103-5. PMID 9323321 DOI: 10.1097/00041444-199723000-00002 |
0.302 |
|
| 1997 |
Didierjean O, Martinez M, Campion D, Hannequin D, Dubois B, Martin C, Puel M, Thomas Anterion C, Pasquier F, Moreau O, Babron MC, Penet C, Agid Y, Clerget-Darpoux F, Frebourg T, et al. No effect of the alpha1-antichymotrypsin A allele in Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 63: 103-5. PMID 9221977 DOI: 10.1136/Jnnp.63.1.103 |
0.408 |
|
| 1997 |
Thibaut F, Ribeyre J, Dourmap N, Meloni R, Laurent C, Campion D, Ménard J, Dollfus S, Mallet J, Petit M. Association of DNA polymorphism in the first intron of the tyrosine hydroxylase gene with disturbances of the catecholaminergic system in schizophrenia Schizophrenia Research. 23: 259-264. PMID 9075305 DOI: 10.1016/S0920-9964(96)00118-1 |
0.313 |
|
| 1996 |
Campion D, Brice A, Dumanchin C, Puel M, Baulac M, De La Sayette V, Hannequin D, Duyckaerts C, Michon A, Martin C, Moreau V, Penet C, Martinez M, Clerget-Darpoux F, Agid Y, et al. A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years. Neuroreport. 7: 1582-4. PMID 8904759 DOI: 10.1097/00001756-199607080-00009 |
0.331 |
|
| 1996 |
Hannequin D, Campion D, Brice A, Frebourg T, Martinez M, Clerget-Darpoux F, Agid Y. Genetics of Alzheimer's disease Revue De Medecine Interne. 17: 545-550. PMID 8881379 DOI: 10.1016/0248-8663(96)83090-6 |
0.36 |
|
| 1996 |
Campion D, Brice A, Hannequin D, Charbonnier F, Dubois B, Martin C, Michon A, Penet C, Bellis M, Calenda A, Martinez M, Agid Y, Clerget-Darpoux F, Frebourg T, Thomas-Anterion C, et al. No founder effect in three novel Alzheimer's disease families with APP 717 Val → Ile mutation Journal of Medical Genetics. 33: 661-664. PMID 8863158 DOI: 10.1136/Jmg.33.8.661 |
0.451 |
|
| 1996 |
Sherrington R, Froelich S, Sorbi S, Campion D, Chi H, Rogaeva EA, Levesque G, Rogaev EI, Lin C, Liang Y, Ikeda M, Mar L, Brice A, Agid Y, Percy ME, et al. Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. Human Molecular Genetics. 5: 985-8. PMID 8817335 DOI: 10.1093/Hmg/5.7.985 |
0.445 |
|
| 1996 |
Bodeau-Péan S, Laurent C, Campion D, Jay M, Thibaut F, Dollfus S, Petit M, Samolyk D, d'Amato T, Martinez M. No evidence for linkage or association between the dopamine transporter gene and schizophrenia in a French population. Psychiatry Research. 59: 1-6. PMID 8771214 DOI: 10.1016/0165-1781(95)02789-0 |
0.313 |
|
| 1996 |
Martinez M, Campion D, Babron MC, Hannequin D, Agid Y, Bellis M, Brice A, Mallet J, Michon A, Thomas-Anterion C, Clerget-Darpoux F, Dubios B, Goas Y, Jaillard-Serradt A, Ledoze F, et al. Segregation analysis of alzheimer pedigrees: Rare mendelian dominant mutation(s) explain a minority of early-onset cases American Journal of Medical Genetics - Seminars in Medical Genetics. 67: 9-12. PMID 8678122 DOI: 10.1002/Ajmg.1320670102 |
0.406 |
|
| 1996 |
Campion D, Brice A, Agid Y, Martinez M, Frebourg T, Clerget-Darpoux F, Dubois B. 784 Genetic studies of Alzheimer's disease in 434 French families Neurobiology of Aging. 17: S195. DOI: 10.1016/S0197-4580(96)80786-X |
0.375 |
|
| 1996 |
Martinez M, Campion D, Hannequin D, Brice A, Freebourg T, Agid Y, Clerget-Darpoux F. 750 On the genetic contribution of Apolipoprotein E e4 allele in Alzheimer's disease transmission Neurobiology of Aging. 17: S186. DOI: 10.1016/S0197-4580(96)80752-4 |
0.322 |
|
| 1995 |
Pérez-Tur J, Campion D, Martinez M, Brice A, Tardieu S, Hannequin D, Agid Y, Delacourte A, Clerget-Darpoux F, Chartier-Harlin MC. Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives. American Journal of Medical Genetics. 60: 550-3. PMID 8825894 DOI: 10.1002/Ajmg.1320600613 |
0.402 |
|
| 1995 |
Campion D, Flaman JM, Brice A, Hannequin D, Dubois B, Martin C, Moreau V, Charbonnier F, Didierjean O, Tardieu S, Penet C, Puel M, Pasquier F, Le Doze F, Bellis G, et al. Mutations of the presenilin I gene in families with early-onset alzheimer's disease Human Molecular Genetics. 4: 2373-2377. PMID 8634712 DOI: 10.1093/Hmg/4.12.2373 |
0.431 |
|
| 1995 |
Campion D, Brice A, Hannequin D, Tardieu S, Dubois B, Calenda A, Brun E, Penet C, Tayot J, Martinez M, Bellis M, Mallet J, Agid Y, Clerget-Darpoux F. A large pedigree with early-onset alzheimer's disease: Clinical, neuropathologic, and genetic characterization Neurology. 45: 80-85. PMID 7824141 DOI: 10.1212/Wnl.45.1.80 |
0.423 |
|
| 1995 |
Campion D, Martin C, Heilig R, Charbonnier F, Moreau V, Flaman JM, Petit JL, Hannequin D, Brice A, Frebourg T. The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease. Genomics. 26: 254-7. PMID 7601450 DOI: 10.1016/0888-7543(95)80208-4 |
0.439 |
|
| 1995 |
Campion D, Martinez M, Hannequin D, Brice A, Thomas-Anterion C, Michon A, Babron MC, Dubois B, Goas Y, Jaillard-Serradt A, Ledoze F, Pasquier F, Puel M, Zimmerman MA, Bellis M, et al. Characteristics of familial aggregation in early-onset Alzheimer's disease: Evidence of subgroups American Journal of Medical Genetics - Neuropsychiatric Genetics. 60: 221-227. PMID 7573175 DOI: 10.1002/Ajmg.1320600310 |
0.348 |
|
| 1995 |
Brice A, Tardieu S, Campion D, Le Guern E, Martinez M, Carpentier A, Penet C, Dubois B, Bellis M, Mallet J, Hannequin D, Clerget-Darpoux F, Agid Y, Michon A, Pillon B, et al. Allelic association at the D14S43 locus in early onset Alzheimer's disease American Journal of Medical Genetics - Neuropsychiatric Genetics. 60: 91-93. PMID 7485257 DOI: 10.1002/Ajmg.1320600202 |
0.46 |
|
| 1994 |
Sabaté O, Campion D, d'Amato T, Martres MP, Sokoloff P, Giros B, Leboyer M, Jay M, Guedj F, Thibaut F. Failure to find evidence for linkage or association between the dopamine D3 receptor gene and schizophrenia. The American Journal of Psychiatry. 151: 107-11. PMID 7903510 DOI: 10.1176/Ajp.151.1.107 |
0.322 |
|
| 1993 |
Carter D, Campion D, d'Amato T, Jay M, Brice A, Bellis M, Mallet J, Agid Y. No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients. Human Molecular Genetics. 2: 321. PMID 8499923 DOI: 10.1093/Hmg/2.3.321 |
0.402 |
|
| 1993 |
Brice A, Boch AL, Stevanin G, Khati C, Dubois B, Agid Y, Campion D, Clerget F, Mallet J, Bellis M. Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 56: 112-3. PMID 8429314 DOI: 10.1136/Jnnp.56.1.112-A |
0.435 |
|
| 1993 |
Martinez M, Campion D, Babron MC, Clerget-Darpoux F. Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)? Genetic Epidemiology. 10: 431-435. PMID 8314039 DOI: 10.1002/Gepi.1370100617 |
0.402 |
|
| 1992 |
Carter DA, Desmarais E, Bellis M, Campion D, Clerget-Darpoux F, Brice A, Agid Y, Jaillard-Serradt A, Mallet J. More missense in amyloid gene Nature Genetics. 2: 255-256. PMID 1303275 DOI: 10.1038/Ng1292-255 |
0.366 |
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