| Year |
Citation |
Score |
| 2024 |
Landoulsi Z, Sreelatha AAK, Schulte C, Bobbili DR, Montanucci L, Leu C, Niestroj LM, Hassanin E, Domenighetti C, Pavelka L, Sugier PE, Radivojkov-Blagojevic M, Lichtner P, Portugal B, Edsall C, ... ... Lesage S, et al. Genome-wide association study of copy number variations in Parkinson's disease. Medrxiv : the Preprint Server For Health Sciences. PMID 39228715 DOI: 10.1101/2024.08.21.24311915 |
0.348 |
|
| 2024 |
Magrinelli F, Tesson C, Angelova PR, Salazar-Villacorta A, Rodriguez JA, Scardamaglia A, Chung BH, Jaconelli M, Vona B, Esteras N, Kwong AK, Courtin T, Maroofian R, Alavi S, Nirujogi R, ... ... Lesage S, et al. variants cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality by disrupting mitochondrial pathways. Medrxiv : the Preprint Server For Health Sciences. PMID 39148840 DOI: 10.1101/2024.06.19.24308302 |
0.378 |
|
| 2024 |
Domenighetti C, Sugier PE, Ashok Kumar Sreelatha A, Schulte C, Grover S, Portugal B, Lee PC, May P, Bobbili D, Radivojkov Blagojevic M, Lichtner P, Singleton AB, Hernandez D, Edsall C, Mellick GD, ... ... Lesage S, et al. Association of Body Mass Index and Parkinson Disease: A Bidirectional Mendelian Randomization Study. Neurology. 103: e209620. PMID 38986057 DOI: 10.1212/WNL.0000000000209620 |
0.329 |
|
| 2024 |
Cogan G, Daida K, Billingsley KJ, Tesson C, Forlani S, Jornea L, Arnaud L, Tissier L, LeGuern E, Singleton AB, Ferrien M, Gervais Bernard H, Lesage S, Blauwendraat C, Brice A. Long-read sequencing unravels the complexity of structural variants in in two individuals with early-onset Parkinson's disease. Medrxiv : the Preprint Server For Health Sciences. PMID 38746197 DOI: 10.1101/2024.05.02.24306523 |
0.396 |
|
| 2024 |
Gustavsson EK, Follett J, Trinh J, Barodia SK, Real R, Liu Z, Grant-Peters M, Fox JD, Appel-Cresswell S, Stoessl AJ, Rajput A, Rajput AH, Auer R, Tilney R, Sturm M, ... ... Lesage S, et al. RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses. The Lancet. Neurology. PMID 38614108 DOI: 10.1016/S1474-4422(24)00121-2 |
0.366 |
|
| 2024 |
Menon PJ, Sambin S, Criniere-Boizet B, Courtin T, Tesson C, Casse F, Ferrien M, Mariani LL, Carvalho S, Lejeune FX, Rebbah S, Martet G, Houot M, Lanore A, Mangone G, ... ... Lesage S, et al. Genotype-phenotype correlation in PRKN-associated Parkinson's disease. Npj Parkinson's Disease. 10: 72. PMID 38553467 DOI: 10.1038/s41531-024-00677-3 |
0.407 |
|
| 2024 |
El Otmani H, Daghi M, Tahiri Jouti N, Lesage S. An overview of the worldwide distribution of mutations in Parkinson's disease. Neurodegenerative Disease Management. 13: 335-350. PMID 38305913 DOI: 10.2217/nmt-2023-0025 |
0.433 |
|
| 2024 |
Gustavsson EK, Follett J, Trinh J, Barodia SK, Real R, Liu Z, Grant-Peters M, Fox JD, Appel-Cresswell S, Stoessl AJ, Rajput A, Rajput AH, Auer R, Tilney R, Sturm M, ... ... Lesage S, et al. A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and . Medrxiv : the Preprint Server For Health Sciences. PMID 38293014 DOI: 10.1101/2024.01.17.24300927 |
0.392 |
|
| 2023 |
Tesson C, Bouchetara MS, Ferrien M, Lesage S, Brice A. Identification of a DAGLB Mutation in a Non-Chinese Patient with Parkinson's Disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 37431851 DOI: 10.1002/mds.29533 |
0.37 |
|
| 2023 |
Bakhit Y, Ibrahim MO, Tesson C, Elhassan AA, Ahmed MA, Alebeed MA, Elrasheed SM, Omar MA, Abubaker R, Eltom K, Shaheen MT, Ibrahim YA, Almak ME, Ali HA, Abugrain AA, ... ... Lesage S, et al. Intrafamilial and interfamilial heterogeneity of PINK1-associated Parkinson's disease in Sudan. Parkinsonism & Related Disorders. 111: 105401. PMID 37150071 DOI: 10.1016/j.parkreldis.2023.105401 |
0.383 |
|
| 2023 |
Bakhit Y, Tesson C, Ibrahim MO, Eltom K, Eltazi I, Elsayed LEO, Lesage S, Seidi O, Corvol JC, Wüllner U. PLA2G6-associated late-onset parkinsonism in a Sudanese family. Annals of Clinical and Translational Neurology. PMID 37139542 DOI: 10.1002/acn3.51781 |
0.3 |
|
| 2023 |
Casse F, Courtin T, Tesson C, Ferrien M, Noël S, Fauret-Amsellem AL, Gareau T, Guegan J, Anheim M, Mariani LL, Le Forestier N, Tranchant C, Corvol JC, Lesage S, Brice A. Detection of Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism. Movement Disorders Clinical Practice. 10: 664-669. PMID 37070044 DOI: 10.1002/mdc3.13699 |
0.349 |
|
| 2023 |
Lesage S, Trinh J. Special Issue "Parkinson's Disease: Genetics and Pathogenesis". Genes. 14. PMID 36981007 DOI: 10.3390/genes14030737 |
0.369 |
|
| 2023 |
Lanore A, Casse F, Tesson C, Courtin T, Menon PJ, Sambin S, Mangone G, Mariani LL, Lesage S, Brice A, Elbaz A, Corvol JC. Differences in survival across monogenic forms of Parkinson's disease. Annals of Neurology. PMID 36905164 DOI: 10.1002/ana.26636 |
0.331 |
|
| 2023 |
Sugier PE, Lucotte EA, Domenighetti C, Law MH, Iles MM, Brown K, Amos C, McKay JD, Hung RJ, Karimi M, Bacq-Daian D, Boland-Augé A, Olaso R, Deleuze JF, Lesueur F, ... ... Lesage S, et al. Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 36788297 DOI: 10.1002/mds.29337 |
0.322 |
|
| 2023 |
Vollstedt EJ, Schaake S, Lohmann K, Padmanabhan S, Brice A, Lesage S, Tesson C, Vidailhet M, Wurster I, Hentati F, Mirelman A, Giladi N, Marder K, Waters C, Fahn S, et al. Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 36692014 DOI: 10.1002/mds.29288 |
0.38 |
|
| 2022 |
Real R, Martinez-Carrasco A, Reynolds RH, Lawton MA, Tan MMX, Shoai M, Corvol JC, Ryten M, Bresner C, Hubbard L, Brice A, Lesage S, Faouzi J, Elbaz A, Artaud F, et al. Association between the LRP1B and APOE loci in the development of Parkinson's disease dementia. Brain : a Journal of Neurology. PMID 36348503 DOI: 10.1093/brain/awac414 |
0.32 |
|
| 2022 |
Fevga C, Tesson C, Mascaro AC, Courtin T, van Coller R, Sakka S, Ferraro F, Farhat N, Bardien S, Damak M, Carr J, Ferrien M, Boumeester V, Hundscheid J, Grillenzoni N, ... ... Lesage S, et al. PTPA variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability. Brain : a Journal of Neurology. PMID 36073231 DOI: 10.1093/brain/awac326 |
0.345 |
|
| 2022 |
Grover S, Kumar Sreelatha AA, Pihlstrom L, Domenighetti C, Schulte C, Sugier PE, Radivojkov-Blagojevic M, Lichtner P, Mohamed O, Portugal B, Landoulsi Z, May P, Bobbili D, Edsall C, Bartusch F, ... ... Lesage S, et al. Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium. Neurology. 99: e698-e710. PMID 35970579 DOI: 10.1212/WNL.0000000000200699 |
0.362 |
|
| 2022 |
Grover S, Ashwin AKS, Pihlstrom L, Domenighetti C, Schulte C, Sugier PE, Radivojkov-Blagojevic M, Lichtner P, Mohamed O, Portugal B, Landoulsi Z, May P, Bobbili D, Edsall C, Bartusch F, ... ... Lesage S, et al. Genome-wide Association and Meta-analysis of Age-at-Onset in Parkinson Disease: Evidence From COURAGE-PD Consortium. Neurology. PMID 35618440 DOI: 10.1212/WNL.0000000000200699 |
0.373 |
|
| 2022 |
Lanore A, Lesage S, Mariani LL, Menon PJ, Ravassard P, Cheval H, Corti O, Brice A, Corvol JC. Does the Expression and Epigenetics of Genes Involved in Monogenic Forms of Parkinson's Disease Influence Sporadic Forms? Genes. 13. PMID 35328033 DOI: 10.3390/genes13030479 |
0.362 |
|
| 2022 |
Domenighetti C, Sugier PE, Ashok Kumar Sreelatha A, Schulte C, Grover S, Mohamed O, Portugal B, May P, Bobbili DR, Radivojkov-Blagojevic M, Lichtner P, Singleton AB, Hernandez DG, Edsall C, Mellick GD, ... ... Lesage S, et al. Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 34997937 DOI: 10.1002/mds.28902 |
0.328 |
|
| 2021 |
Courtin T, Tesson C, Corvol JC, Lesage S, Brice A. Lack of evidence for association of UQCRC1 with autosomal dominant Parkinson's disease in Caucasian families. Neurogenetics. PMID 34286409 DOI: 10.1007/s10048-021-00647-4 |
0.34 |
|
| 2021 |
Liu G, Peng J, Liao Z, Locascio JJ, Corvol JC, Zhu F, Dong X, Maple-Grødem J, Campbell MC, Elbaz A, Lesage S, Brice A, Mangone G, Growdon JH, Hung AY, et al. Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's disease. Nature Genetics. PMID 33958783 DOI: 10.1038/s41588-021-00847-6 |
0.36 |
|
| 2021 |
Blauwendraat C, Iwaki H, Makarious MB, Bandres-Ciga S, Leonard H, Grenn FP, Lake J, Krohn L, Tan M, Kim JJ, Gibbs JR, Hernandez DG, Ruskey JA, Pihlstrøm L, Toft M, ... ... Lesage S, ... ... Lesage S, et al. Investigation of Autosomal Genetic Sex Differences in Parkinson's disease. Annals of Neurology. PMID 33901317 DOI: 10.1002/ana.26090 |
0.376 |
|
| 2021 |
Lesage S, Mangone G, Tesson C, Bertrand H, Benmahdjoub M, Kesraoui S, Arezki M, Singleton A, Corvol JC, Brice A. Clinical Variability of -Associated Early-Onset Parkinsonism. Frontiers in Neurology. 12: 648457. PMID 33841314 DOI: 10.3389/fneur.2021.648457 |
0.426 |
|
| 2020 |
Lesage S, Lunati A, Houot M, Romdhan SB, Clot F, Tesson C, Mangone G, Toullec BL, Courtin T, Larcher K, Benmahdjoub M, Arezki M, Bouhouche A, Anheim M, Roze E, et al. Characterization of Recessive Parkinson Disease in a Large Multicenter Study. Annals of Neurology. 88: 843-850. PMID 33045815 DOI: 10.1002/ana.25787 |
0.407 |
|
| 2020 |
Tesson C, Lohmann E, Devos D, Bertrand H, Lesage S, Brice A. Segregation of ATP10B variants in families with autosomal recessive parkinsonism. Acta Neuropathologica. PMID 32892229 DOI: 10.1007/s00401-020-02219-6 |
0.327 |
|
| 2020 |
Brown EE, Blauwendraat C, Trinh J, Rizig M, Nalls MA, Leveille E, Ruskey JA, Jonvik H, Tan MMX, Bandres-Ciga S, Hassin-Baer S, Brockmann K, Infante J, Tolosa E, Ezquerra M, ... ... Lesage S, et al. Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's disease. Neurobiology of Aging. PMID 32873436 DOI: 10.1016/J.Neurobiolaging.2020.07.002 |
0.514 |
|
| 2020 |
Mangone G, Bekadar S, Cormier-Dequaire F, Tahiri K, Welaratne A, Czernecki V, Pineau F, Karachi C, Castrioto A, Durif F, Tranchant C, Devos D, Thobois S, Meissner WG, Navarro MS, ... ... Lesage S, et al. Early cognitive decline after bilateral subthalamic deep brain stimulation in Parkinson's disease patients with GBA mutations. Parkinsonism & Related Disorders. 76: 56-62. PMID 32866938 DOI: 10.1016/J.Parkreldis.2020.04.002 |
0.46 |
|
| 2020 |
Lesage S, Houot M, Mangone G, Tesson C, Bertrand H, Forlani S, Anheim M, Brefel-Courbon C, Broussolle E, Thobois S, Damier P, Durif F, Roze E, Tison F, Grabli D, et al. Genetic and Phenotypic Basis of Autosomal Dominant Parkinson's Disease in a Large Multi-Center Cohort. Frontiers in Neurology. 11: 682. PMID 32849182 DOI: 10.3389/Fneur.2020.00682 |
0.555 |
|
| 2020 |
Prud'hon S, Bekadar S, Rastetter A, Guégan J, Cormier-Dequaire F, Lacomblez L, Mangone G, You H, Daniau M, Marie Y, Bertrand H, Lesage S, Tezenas Du Montcel S, Anheim M, Brice A, et al. Exome Sequencing Reveals Signal Transduction Genes Involved in Impulse Control Disorders in Parkinson's Disease. Frontiers in Neurology. 11: 641. PMID 32793093 DOI: 10.3389/Fneur.2020.00641 |
0.478 |
|
| 2020 |
Smaili I, Tesson C, Regragui W, Bertrand H, Rahmani M, Bouslam N, Benomar A, Brice A, Lesage S, Bouhouche A. Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease. Journal of Molecular Neuroscience : Mn. PMID 32557143 DOI: 10.1007/S12031-020-01635-3 |
0.546 |
|
| 2020 |
Lesage S, Lunati A, Houot M, Romdhan SB, Clot F, Tesson C, Mangone G, Toullec BL, Courtin T, Larcher K, Benmahdjoub M, Arezki M, Bouhouche A, Anheim M, Roze E, et al. Characterization of recessive Parkinson's disease in a large multicenter study. Annals of Neurology. PMID 32472966 DOI: 10.1002/Ana.25787 |
0.502 |
|
| 2020 |
Ihle J, Artaud F, Bekadar S, Mangone G, Sambin S, Mariani LL, Bertrand H, Rascol O, Durif F, Derkinderen P, Scherzer C, Elbaz A, Corvol JC, Corvol JC, ... ... Lesage S, et al. Parkinson's disease polygenic risk score is not associated with impulse control disorders: A longitudinal study. Parkinsonism & Related Disorders. 75: 30-33. PMID 32450545 DOI: 10.1016/J.Parkreldis.2020.03.017 |
0.429 |
|
| 2020 |
Orme T, Hernandez D, Ross OA, Kun-Rodrigues C, Darwent L, Shepherd CE, Parkkinen L, Ansorge O, Clark L, Honig LS, Marder K, Lemstra A, Rogaeva E, St George-Hyslop P, Londos E, ... ... Lesage S, et al. Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies. Acta Neuropathologica Communications. 8: 5. PMID 31996268 DOI: 10.1186/S40478-020-0879-Z |
0.475 |
|
| 2019 |
Blauwendraat C, Reed X, Krohn L, Heilbron K, Bandres-Ciga S, Tan M, Gibbs JR, Hernandez DG, Kumaran R, Langston R, Bonet-Ponce L, Alcalay RN, Hassin-Baer S, Greenbaum L, Iwaki H, ... ... Lesage S, et al. Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia. Brain : a Journal of Neurology. PMID 31755958 DOI: 10.1093/Brain/Awz350 |
0.443 |
|
| 2019 |
Nalls MA, Blauwendraat C, Vallerga CL, Heilbron K, Bandres-Ciga S, Chang D, Tan M, Kia DA, Noyce AJ, Xue A, Bras J, Young E, von Coelln R, Simón-Sánchez J, Schulte C, ... ... Lesage S, et al. Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies. The Lancet. Neurology. 18: 1091-1102. PMID 31701892 DOI: 10.1016/S1474-4422(19)30320-5 |
0.392 |
|
| 2019 |
Blauwendraat C, Heilbron K, Vallerga CL, Bandres-Ciga S, von Coelln R, Pihlstrøm L, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Siitonen A, Iwaki H, Leonard H, Noyce AJ, Tan M, ... ... Lesage S, et al. Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 30957308 DOI: 10.1002/Mds.27659 |
0.447 |
|
| 2019 |
Guerreiro R, Escott-Price V, Hernandez DG, Kun-Rodrigues C, Ross OA, Orme T, Neto JL, Carmona S, Dehghani N, Eicher JD, Shepherd C, Parkkinen L, Darwent L, Heckman MG, Scholz SW, ... ... Lesage S, et al. Heritability and genetic variance of dementia with Lewy bodies. Neurobiology of Disease. PMID 30953760 DOI: 10.1016/J.Nbd.2019.04.004 |
0.415 |
|
| 2019 |
Bonello F, Hassoun SM, Mouton-Liger F, Shin YS, Muscat A, Tesson C, Lesage S, Beart PM, Brice A, Krupp J, Corvol JC, Corti O. LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson's disease. Human Molecular Genetics. PMID 30629163 DOI: 10.1093/Hmg/Ddz004 |
0.453 |
|
| 2018 |
Lassot I, Mora S, Lesage S, Zieba BA, Coque E, Condroyer C, Bossowski JP, Mojsa B, Marelli C, Soulet C, Tesson C, Carballo-Carbajal I, Laguna A, Mangone G, Vila M, et al. The E3 Ubiquitin Ligases TRIM17 and TRIM41 Modulate α-Synuclein Expression by Regulating ZSCAN21. Cell Reports. 25: 2484-2496.e9. PMID 30485814 DOI: 10.1016/J.Celrep.2018.11.002 |
0.413 |
|
| 2018 |
Kun-Rodrigues C, Orme T, Carmona S, Hernandez DG, Ross OA, Eicher JD, Shepherd C, Parkkinen L, Darwent L, Heckman MG, Scholz SW, Troncoso JC, Pletnikova O, Dawson T, Rosenthal L, ... ... Lesage S, et al. A comprehensive screening of copy number variability in dementia with Lewy bodies. Neurobiology of Aging. PMID 30448004 DOI: 10.1016/J.Neurobiolaging.2018.10.019 |
0.366 |
|
| 2018 |
Cormier-Dequaire F, Bekadar S, Anheim M, Lebbah S, Pelissolo A, Krack P, Lacomblez L, Lhommée E, Castrioto A, Azulay JP, Defebvre L, Kreisler A, Durif F, Marques-Raquel A, Brefel-Courbon C, ... ... Lesage S, et al. Suggestive association between OPRM1 and impulse control disorders in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 30444952 DOI: 10.1002/Mds.27519 |
0.432 |
|
| 2018 |
Lunati A, Lesage S, Brice A. The genetic landscape of Parkinson's disease. Revue Neurologique. 174: 628-643. PMID 30245141 DOI: 10.1016/J.Neurol.2018.08.004 |
0.559 |
|
| 2018 |
Emelyanov AK, Usenko TS, Tesson C, Senkevich KA, Nikolaev MA, Miliukhina IV, Kopytova AE, Timofeeva AA, Yakimovsky AF, Lesage S, Brice A, Pchelina SN. Mutation analysis of Parkinson's disease genes in a Russian data set. Neurobiology of Aging. PMID 30146349 DOI: 10.1016/J.Neurobiolaging.2018.06.027 |
0.53 |
|
| 2018 |
Blauwendraat C, Reed X, Kia DA, Gan-Or Z, Lesage S, Pihlstrøm L, Guerreiro R, Gibbs JR, Sabir M, Ahmed S, Ding J, Alcalay RN, Hassin-Baer S, Pittman AM, Brooks J, et al. Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease. Jama Neurology. PMID 30039155 DOI: 10.1001/Jamaneurol.2018.1885 |
0.473 |
|
| 2018 |
Ben Romdhan S, Farhat N, Nasri A, Lesage S, Hdiji O, Ben Djebara M, Landoulsi Z, Stevanin G, Brice A, Damak M, Gouider R, Mhiri C. LRRK2 G2019S Parkinson's disease with more benign phenotype than idiopathic. Acta Neurologica Scandinavica. PMID 29989150 DOI: 10.1111/Ane.12996 |
0.462 |
|
| 2018 |
Guerreiro R, Ross OA, Kun-Rodrigues C, Hernandez DG, Orme T, Eicher JD, Shepherd CE, Parkkinen L, Darwent L, Heckman MG, Scholz SW, Troncoso JC, Pletnikova O, Ansorge O, Clarimon J, ... ... Lesage S, et al. Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study. The Lancet. Neurology. 17: 64-74. PMID 29263008 DOI: 10.1016/S1474-4422(17)30400-3 |
0.339 |
|
| 2017 |
Blauwendraat C, Kia DA, Pihlstrøm L, Gan-Or Z, Lesage S, Gibbs JR, Ding J, Alcalay RN, Hassin-Baer S, Pittman AM, Brooks J, Edsall C, Chung SJ, Goldwurm S, Toft M, et al. Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease. Neurobiology of Aging. PMID 29398121 DOI: 10.1016/J.Neurobiolaging.2017.12.012 |
0.524 |
|
| 2017 |
Bouhouche A, Tesson C, Regragui W, Rahmani M, Drouet V, Tibar H, Souirti Z, Ben El Haj R, Bouslam N, Yahyaoui M, Brice A, Benomar A, Lesage S. Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel. Frontiers in Neurology. 8: 567. PMID 29163333 DOI: 10.3389/Fneur.2017.00567 |
0.549 |
|
| 2017 |
Shamir R, Klein C, Amar D, Vollstedt EJ, Bonin M, Usenovic M, Wong YC, Maver A, Poths S, Safer H, Corvol JC, Lesage S, Lavi O, Deuschl G, Kuhlenbaeumer G, et al. Analysis of blood-based gene expression in idiopathic Parkinson disease. Neurology. PMID 28916538 DOI: 10.1212/Wnl.0000000000004516 |
0.451 |
|
| 2017 |
Lee AJ, Wang Y, Alcalay RN, Mejia-Santana H, Saunders-Pullman R, Bressman S, Corvol JC, Brice A, Lesage S, Mangone G, Tolosa E, Pont-Sunyer C, Vilas D, Schüle B, Kausar F, et al. Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 28639421 DOI: 10.1002/Mds.27059 |
0.361 |
|
| 2017 |
Blauwendraat C, Faghri F, Pihlstrom L, Geiger JT, Elbaz A, Lesage S, Corvol JC, May P, Nicolas A, Abramzon Y, Murphy NA, Gibbs JR, Ryten M, Ferrari R, Bras J, et al. NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases. Neurobiology of Aging. PMID 28602509 DOI: 10.1016/J.Neurobiolaging.2017.05.009 |
0.385 |
|
| 2017 |
Witoelar A, Jansen IE, Wang Y, Desikan RS, Gibbs JR, Blauwendraat C, Thompson WK, Hernandez DG, Djurovic S, Schork AJ, Bettella F, Ellinghaus D, Franke A, Lie BA, McEvoy LK, ... ... Lesage S, et al. Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases. Jama Neurology. PMID 28586827 DOI: 10.1001/Jamaneurol.2017.0469 |
0.426 |
|
| 2017 |
Jansen IE, Ye H, Heetveld S, Lechler MC, Michels H, Seinstra RI, Lubbe SJ, Drouet V, Lesage S, Majounie E, Gibbs JR, Nalls MA, Ryten M, Botia JA, Vandrovcova J, et al. Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Genome Biology. 18: 22. PMID 28137300 DOI: 10.1186/S13059-017-1147-9 |
0.484 |
|
| 2016 |
Giri A, Mok KY, Jansen I, Sharma M, Tesson C, Mangone G, Lesage S, Bras JM, Shulman J, Sheerin UM, Díez-Fairen M, Pastor P, Martí MJ, Ezquerra M, et al. Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population. Neurobiology of Aging. PMID 27818000 DOI: 10.1016/J.Neurobiolaging.2016.10.004 |
0.511 |
|
| 2016 |
Wang L, Heckman MG, Aasly JO, Annesi G, Bozi M, Chung SJ, Clarke C, Crosiers D, Eckstein G, Garraux G, Hadjigeorgiou GM, Hattori N, Jeon B, Kim YJ, Kubo M, ... Lesage S, et al. Evaluation of the interaction between LRRK2 and PARK16 loci in determining risk of Parkinson's disease: analysis of a large multicenter study. Neurobiology of Aging. PMID 27814993 DOI: 10.1016/J.Neurobiolaging.2016.09.022 |
0.467 |
|
| 2016 |
Lubbe SJ, Escott-Price V, Gibbs JR, Nalls MA, Bras J, Price TR, Nicolas A, Jansen IE, Mok KY, Pittman AM, Tomkins JE, Lewis PA, Noyce AJ, Lesage S, Sharma M, et al. Additional Rare Variant Analysis in Parkinson's Disease Cases with and Without Known Pathogenic Mutations: Evidence for Oligogenic Inheritance. Human Molecular Genetics. PMID 27798102 DOI: 10.1093/Hmg/Ddw348 |
0.547 |
|
| 2016 |
Trinh J, Gustavsson EK, Vilariño-Güell C, Bortnick S, Latourelle J, McKenzie MB, Tu CS, Nosova E, Khinda J, Milnerwood A, Lesage S, Brice A, Tazir M, Aasly JO, Parkkinen L, et al. DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. The Lancet. Neurology. PMID 27692902 DOI: 10.1016/S1474-4422(16)30203-4 |
0.435 |
|
| 2016 |
Kun-Rodrigues C, Ross OA, Orme T, Shepherd C, Parkkinen L, Darwent L, Hernandez D, Ansorge O, Clark LN, Honig LS, Marder K, Lemstra A, Scheltens P, van der Flier W, Louwersheimer E, ... ... Lesage S, et al. Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies. Neurobiology of Aging. PMID 27666590 DOI: 10.1016/J.Neurobiolaging.2016.08.023 |
0.315 |
|
| 2016 |
Mok KY, Sheerin U, Simón-Sánchez J, Salaka A, Chester L, Escott-Price V, Mantripragada K, Doherty KM, Noyce AJ, Mencacci NE, Lubbe SJ, Williams-Gray CH, Barker RA, van Dijk KD, ... ... Lesage S, et al. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data. The Lancet. Neurology. PMID 27017469 DOI: 10.1016/S1474-4422(16)00071-5 |
0.394 |
|
| 2016 |
Degos B, Toussaint A, Lesage S, Brice A, Vidailhet M, Beldjord C, Catala M. PINK1 and FLNA mutations association: A role for atypical parkinsonism? Parkinsonism & Related Disorders. PMID 26969111 DOI: 10.1016/J.Parkreldis.2016.02.023 |
0.451 |
|
| 2016 |
Lesage S, Drouet V, Majounie E, Deramecourt V, Jacoupy M, Nicolas A, Cormier-Dequaire F, Hassoun SM, Pujol C, Ciura S, Erpapazoglou Z, Usenko T, Maurage CA, Sahbatou M, Liebau S, et al. Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy. American Journal of Human Genetics. 98: 500-13. PMID 26942284 DOI: 10.1016/J.Ajhg.2016.01.014 |
0.476 |
|
| 2016 |
Sayad M, Zouambia M, Chaouch M, Ferrat F, Nebbal M, Bendini M, Lesage S, Brice A, Brahim Errahmani M, Asselah B. Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers. Bmc Neuroscience. 17: 6. PMID 26831335 DOI: 10.1186/S12868-016-0240-4 |
0.471 |
|
| 2016 |
Elsayed LE, Drouet V, Usenko T, Mohammed IN, Hamed AA, Elseed MA, Salih MA, Koko ME, Mohamed AY, Siddig RA, Elbashir MI, Ibrahim ME, Durr A, Stevanin G, Lesage S, et al. A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease. Annals of Neurology. 79: 335-7. PMID 26703368 DOI: 10.1002/Ana.24591 |
0.493 |
|
| 2016 |
Hu HH, Kannengiesser C, Lesage S, André J, Mourah S, Michel L, Descamps V, Basset-Seguin N, Bagot M, Bensussan A, Lebbé C, Deschamps L, Saiag P, Leccia MT, Bressac-de-Paillerets B, et al. PARKIN Inactivation Links Parkinson's Disease to Melanoma. Journal of the National Cancer Institute. 108. PMID 26683220 DOI: 10.1093/Jnci/Djv340 |
0.45 |
|
| 2016 |
Elsayed LEO, Drouet V, Usenko T, Mohammed IN, Hamed AAA, Elseed MA, Salih MAM, Koko ME, Mohamed AYO, Siddig RA, Elbashir MI, Ibrahim ME, Durr A, Stevanin G, Lesage S, et al. A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal-Recessive Juvenile-Onset Parkinson's Disease Annals of Neurology. DOI: 10.1002/ana.24591 |
0.398 |
|
| 2015 |
Lesage S, Bras J, Cormier-Dequaire F, Condroyer C, Nicolas A, Darwent L, Guerreiro R, Majounie E, Federoff M, Heutink P, Wood NW, Gasser T, Hardy J, Tison F, Singleton A, et al. Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson disease. Neurology. Genetics. 1: e9. PMID 27066548 DOI: 10.1212/Nxg.0000000000000009 |
0.515 |
|
| 2015 |
Kun-Rodrigues C, Ganos C, Guerreiro R, Schneider SA, Schulte C, Lesage S, Darwent L, Holmans P, Singleton A, Bhatia K, Bras J. A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease. Human Molecular Genetics. PMID 26362251 DOI: 10.1093/Hmg/Ddv376 |
0.562 |
|
| 2015 |
Wang L, Aasly JO, Annesi G, Bardien S, Bozi M, Brice A, Carr J, Chung SJ, Clarke C, Crosiers D, Deutschländer A, Eckstein G, Farrer MJ, Goldwurm S, Garraux G, ... ... Lesage S, et al. Large-scale assessment of polyglutamine repeat expansions in Parkinson disease. Neurology. PMID 26354989 DOI: 10.1212/Wnl.0000000000002016 |
0.434 |
|
| 2015 |
Nalls MA, McLean CY, Rick J, Eberly S, Hutten SJ, Gwinn K, Sutherland M, Martinez M, Heutink P, Williams NM, Hardy J, Gasser T, Brice A, Price TR, Nicolas A, ... ... Lesage S, et al. Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study. The Lancet. Neurology. 14: 1002-9. PMID 26271532 DOI: 10.1016/S1474-4422(15)00178-7 |
0.383 |
|
| 2015 |
Nichols N, Bras JM, Hernandez DG, Jansen IE, Lesage S, Lubbe S, Singleton AB. EIF4G1 mutations do not cause Parkinson's disease. Neurobiology of Aging. 36: 2444.e1-4. PMID 26022768 DOI: 10.1016/J.Neurobiolaging.2015.04.017 |
0.522 |
|
| 2015 |
Lohmann E, Coquel AS, Honoré A, Gurvit H, Hanagasi H, Emre M, Leutenegger AL, Drouet V, Sahbatou M, Guven G, Erginel-Unaltuna N, Deleuze JF, Lesage S, Brice A. A new F-box protein 7 gene mutation causing typical Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 1130-3. PMID 26010069 DOI: 10.1002/Mds.26266 |
0.459 |
|
| 2015 |
Tomiyama H, Lesage S, Tan EK, Jeon BS. Familial Parkinson's disease/parkinsonism. Biomed Research International. 2015: 736915. PMID 25961036 DOI: 10.1155/2015/736915 |
0.503 |
|
| 2014 |
Theuns J, Verstraeten A, Sleegers K, Wauters E, Gijselinck I, Smolders S, Crosiers D, Corsmit E, Elinck E, Sharma M, Krüger R, Lesage S, Brice A, Chung SJ, Kim MJ, et al. Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease. Neurology. 83: 1906-13. PMID 25326098 DOI: 10.1212/Wnl.0000000000001012 |
0.465 |
|
| 2014 |
Drouet V, Lesage S. Synaptojanin 1 mutation in Parkinson's disease brings further insight into the neuropathological mechanisms. Biomed Research International. 2014: 289728. PMID 25302295 DOI: 10.1155/2014/289728 |
0.459 |
|
| 2014 |
Mencacci NE, Isaias IU, Reich MM, Ganos C, Plagnol V, Polke JM, Bras J, Hersheson J, Stamelou M, Pittman AM, Noyce AJ, Mok KY, Opladen T, Kunstmann E, Hodecker S, ... ... Lesage S, et al. Parkinson's disease in GTP cyclohydrolase 1 mutation carriers. Brain : a Journal of Neurology. 137: 2480-92. PMID 24993959 DOI: 10.1093/Brain/Awu179 |
0.455 |
|
| 2014 |
Nava C, Dalle C, Rastetter A, Striano P, de Kovel CG, Nabbout R, Cancès C, Ville D, Brilstra EH, Gobbi G, Raffo E, Bouteiller D, Marie Y, Trouillard O, Robbiano A, ... ... Lesage S, et al. De novo mutations in HCN1 cause early infantile epileptic encephalopathy. Nature Genetics. 46: 640-5. PMID 24747641 DOI: 10.1038/Ng.2952 |
0.394 |
|
| 2014 |
Chung SJ, Biernacka JM, Armasu SM, Anderson K, Frigerio R, Aasly JO, Annesi G, Bentivoglio AR, Brighina L, Chartier-Harlin MC, Goldwurm S, Hadjigeorgiou G, Jasinska-Myga B, Jeon BS, Kim YJ, ... ... Lesage S, et al. Alpha-synuclein repeat variants and survival in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 29: 1053-7. PMID 24578302 DOI: 10.1002/Mds.25841 |
0.423 |
|
| 2013 |
Trabzuni D, Ryten M, Emmett W, Ramasamy A, Lackner KJ, Zeller T, Walker R, Smith C, Lewis PA, Mamais A, de Silva R, Vandrovcova J, Hernandez D, Nalls MA, ... ... Lesage S, et al. Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus. Plos One. 8: e70724. PMID 23967090 DOI: 10.1371/Journal.Pone.0070724 |
0.432 |
|
| 2013 |
Heckman MG, Soto-Ortolaza AI, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, ... ... Lesage S, et al. Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 1740-4. PMID 23913756 DOI: 10.1002/Mds.25600 |
0.481 |
|
| 2013 |
Nalls MA, Duran R, Lopez G, Kurzawa-Akanbi M, McKeith IG, Chinnery PF, Morris CM, Theuns J, Crosiers D, Cras P, Engelborghs S, De Deyn PP, Van Broeckhoven C, Mann DM, Snowden J, ... ... Lesage S, et al. A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies. Jama Neurology. 70: 727-35. PMID 23588557 DOI: 10.1001/Jamaneurol.2013.1925 |
0.506 |
|
| 2013 |
Lesage S, Anheim M, Letournel F, Bousset L, Honoré A, Rozas N, Pieri L, Madiona K, Dürr A, Melki R, Verny C, Brice A. G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome. Annals of Neurology. 73: 459-71. PMID 23526723 DOI: 10.1002/Ana.23894 |
0.498 |
|
| 2013 |
Stogmann E, Reinthaler E, Eltawil S, El Etribi MA, Hemeda M, El Nahhas N, Gaber AM, Fouad A, Edris S, Benet-Pages A, Eck SH, Pataraia E, Mei D, Brice A, Lesage S, et al. Autosomal recessive cortical myoclonic tremor and epilepsy: association with a mutation in the potassium channel associated gene CNTN2. Brain : a Journal of Neurology. 136: 1155-60. PMID 23518707 DOI: 10.1093/Brain/Awt068 |
0.41 |
|
| 2013 |
Lesage S, Le Ber I, Condroyer C, Broussolle E, Gabelle A, Thobois S, Pasquier F, Mondon K, Dion PA, Rochefort D, Rouleau GA, Dürr A, Brice A. C9orf72 repeat expansions are a rare genetic cause of parkinsonism. Brain : a Journal of Neurology. 136: 385-91. PMID 23413259 DOI: 10.1093/Brain/Aws357 |
0.474 |
|
| 2013 |
Klebe S, Golmard JL, Nalls MA, Saad M, Singleton AB, Bras JM, Hardy J, Simon-Sanchez J, Heutink P, Kuhlenbäumer G, Charfi R, Klein C, Hagenah J, Gasser T, Wurster I, ... Lesage S, et al. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism. Journal of Neurology, Neurosurgery, and Psychiatry. 84: 666-73. PMID 23408064 DOI: 10.1136/Jnnp-2012-304475 |
0.436 |
|
| 2013 |
Hamadouche T, Belarbi S, Hecham N, Lesage S, Brice A, Tazir M, Benhassine T. Diagnostic génétique de la forme PARK8 de la maladie de Parkinson en Algérie par recherche de la mutation c 6055G>A (p gly2019ser) dans le gène LRRK2 Revue Neurologique. 169. DOI: 10.1016/J.Neurol.2013.01.291 |
0.328 |
|
| 2012 |
Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Bertram L, Bozi M, Barcikowska M, Crosiers D, Clarke CE, Facheris MF, Farrer M, Garraux G, Gispert S, Auburger G, ... ... Lesage S, et al. A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Journal of Medical Genetics. 49: 721-6. PMID 23125461 DOI: 10.1136/Jmedgenet-2012-101155 |
0.485 |
|
| 2012 |
Sharma M, Ioannidis JP, Aasly JO, Annesi G, Brice A, Van Broeckhoven C, Bertram L, Bozi M, Crosiers D, Clarke C, Facheris M, Farrer M, Garraux G, Gispert S, Auburger G, ... ... Lesage S, et al. Large-scale replication and heterogeneity in Parkinson disease genetic loci. Neurology. 79: 659-67. PMID 22786590 DOI: 10.1212/Wnl.0B013E318264E353 |
0.417 |
|
| 2012 |
Mittag F, Büchel F, Saad M, Jahn A, Schulte C, Bochdanovits Z, Simón-Sánchez J, Nalls MA, Keller M, Hernandez DG, Gibbs JR, Lesage S, Brice A, Heutink P, Martinez M, et al. Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities. Human Mutation. 33: 1708-18. PMID 22777693 DOI: 10.1002/Humu.22161 |
0.408 |
|
| 2012 |
Lesage S, Condroyer C, Klebe S, Lohmann E, Durif F, Damier P, Tison F, Anheim M, Honoré A, Viallet F, Bonnet AM, Ouvrard-Hernandez AM, Vidailhet M, Durr A, Brice A, et al. EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants? Neurobiology of Aging. 33: 2233.e1-2233.e5. PMID 22658323 DOI: 10.1016/J.Neurobiolaging.2012.05.006 |
0.528 |
|
| 2012 |
Edvardson S, Cinnamon Y, Ta-Shma A, Shaag A, Yim YI, Zenvirt S, Jalas C, Lesage S, Brice A, Taraboulos A, Kaestner KH, Greene LE, Elpeleg O. A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism. Plos One. 7: e36458. PMID 22563501 DOI: 10.1371/Journal.Pone.0036458 |
0.443 |
|
| 2012 |
Lesage S, Condroyer C, Klebe S, Honoré A, Tison F, Brefel-Courbon C, Dürr A, Brice A. Clinical/scientific notes Neurology. 78: 1449-1450. PMID 22517097 DOI: 10.1212/Wnl.0B013E318253D5F2 |
0.545 |
|
| 2012 |
Anheim M, Elbaz A, Lesage S, Durr A, Condroyer C, Viallet F, Pollak P, Bonaïti B, Bonaïti-Pellié C, Brice A. Penetrance of Parkinson disease in glucocerebrosidase gene mutation carriers. Neurology. 78: 417-20. PMID 22282650 DOI: 10.1212/Wnl.0B013E318245F476 |
0.546 |
|
| 2012 |
Lohmann E, Dursun B, Lesage S, Hanagasi HA, Sevinc G, Honore A, Bilgic B, Gürvit H, Dogu O, Kaleagası H, Babacan G, Yazici J, Erginel-Unaltuna N, Brice A, Emre M. Genetic bases and phenotypes of autosomal recessive Parkinson disease in a Turkish population. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 19: 769-75. PMID 22233331 DOI: 10.1111/J.1468-1331.2011.03639.X |
0.527 |
|
| 2012 |
Lesage S, Brice A. Role of mendelian genes in "sporadic" Parkinson's disease. Parkinsonism & Related Disorders. 18: S66-70. PMID 22166458 DOI: 10.1016/S1353-8020(11)70022-0 |
0.527 |
|
| 2011 |
Corti O, Lesage S, Brice A. What genetics tells us about the causes and mechanisms of Parkinson's disease. Physiological Reviews. 91: 1161-218. PMID 22013209 DOI: 10.1152/Physrev.00022.2010 |
0.514 |
|
| 2011 |
Hanagasi HA, Lohmann E, Dursun B, Honoré A, Lesage S, Dogu O, Kaleagasi H, Aydın O, Gürvit H, Erginel-Unaltuna N, Brice A, Emre M. LRRK2 mutations are uncommon in Turkey. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 18: e137. PMID 21914047 DOI: 10.1111/J.1468-1331.2011.03471.X |
0.384 |
|
| 2011 |
Ross OA, Soto-Ortolaza AI, Heckman MG, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Van Broeckhoven C, Carr J, Chartier-Harlin MC, Dardiotis E, ... ... Lesage S, et al. Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study. The Lancet. Neurology. 10: 898-908. PMID 21885347 DOI: 10.1016/S1474-4422(11)70175-2 |
0.524 |
|
| 2011 |
Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée A, Djarmati A, Elbaz A, Farrer M, ... ... Lesage S, et al. Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease. Neurobiology of Aging. 32: 2108.e1-5. PMID 21782285 DOI: 10.1016/J.Neurobiolaging.2011.05.024 |
0.503 |
|
| 2011 |
Bardien S, Lesage S, Brice A, Carr J. Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's disease Parkinsonism and Related Disorders. 17: 501-508. PMID 21641266 DOI: 10.1016/J.Parkreldis.2010.11.008 |
0.542 |
|
| 2011 |
Nalls MA, Plagnol V, Hernandez DG, Sharma M, Sheerin UM, Saad M, Simón-Sánchez J, Schulte C, Lesage S, Sveinbjörnsdóttir S, Stefánsson K, Martinez M, Hardy J, Heutink P, et al. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet. 377: 641-9. PMID 21292315 DOI: 10.1016/S0140-6736(10)62345-8 |
0.403 |
|
| 2011 |
Lesage S, Condroyer C, Hecham N, Anheim M, Belarbi S, Lohman E, Viallet F, Pollak P, Abada M, Dürr A, Tazir M, Brice A. Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa. Neurology. 76: 301-3. PMID 21242499 DOI: 10.1212/Wnl.0B013E318207B01E |
0.521 |
|
| 2011 |
Saad M, Lesage S, Saint-Pierre A, Corvol JC, Zelenika D, Lambert JC, Vidailhet M, Mellick GD, Lohmann E, Durif F, Pollak P, Damier P, Tison F, Silburn PA, Tzourio C, et al. Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. Human Molecular Genetics. 20: 615-27. PMID 21084426 DOI: 10.1093/Hmg/Ddq497 |
0.421 |
|
| 2011 |
Lesage S, Anheim M, Condroyer C, Pollak P, Durif F, Dupuits C, Viallet F, Lohmann E, Corvol JC, Honoré A, Rivaud S, Vidailhet M, Dürr A, Brice A. Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease. Human Molecular Genetics. 20: 202-10. PMID 20947659 DOI: 10.1093/Hmg/Ddq454 |
0.554 |
|
| 2011 |
Krüger R, Sharma M, Riess O, Gasser T, Van Broeckhoven C, Theuns J, Aasly J, Annesi G, Bentivoglio AR, Brice A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, ... ... Lesage S, et al. A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease. Neurobiology of Aging. 32: 548.e9-18. PMID 20036034 DOI: 10.1016/J.Neurobiolaging.2009.11.021 |
0.473 |
|
| 2010 |
Belarbi S, Hecham N, Lesage S, Kediha MI, Smail N, Benhassine T, Ysmail-Dahlouk F, Lohman E, Benhabyles B, Hamadouche T, Assami S, Brice A, Tazir M. LRRK2 G2019S mutation in Parkinson's disease: a neuropsychological and neuropsychiatric study in a large Algerian cohort. Parkinsonism & Related Disorders. 16: 676-9. PMID 20933457 DOI: 10.1016/J.Parkreldis.2010.09.003 |
0.4 |
|
| 2010 |
Troiano AR, Elbaz A, Lohmann E, Belarbi S, Vidailhet M, Bonnet AM, Lesage S, Pollak P, Cazeneuve C, Borg M, Feingold J, Dürr A, Tazir M, Brice A. Low disease risk in relatives of north african lrrk2 Parkinson disease patients. Neurology. 75: 1118-9. PMID 20855856 DOI: 10.1212/Wnl.0B013E3181F39A2E |
0.528 |
|
| 2010 |
Vitte J, Traver S, Maués De Paula A, Lesage S, Rovelli G, Corti O, Duyckaerts C, Brice A. Leucine-rich repeat kinase 2 is associated with the endoplasmic reticulum in dopaminergic neurons and accumulates in the core of Lewy bodies in Parkinson disease. Journal of Neuropathology and Experimental Neurology. 69: 959-72. PMID 20720502 DOI: 10.1097/Nen.0B013E3181Efc01C |
0.47 |
|
| 2010 |
Mitsui J, Takahashi Y, Goto J, Tomiyama H, Ishikawa S, Yoshino H, Minami N, Smith DI, Lesage S, Aburatani H, Nishino I, Brice A, Hattori N, Tsuji S. Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines. American Journal of Human Genetics. 87: 75-89. PMID 20598272 DOI: 10.1016/J.Ajhg.2010.06.006 |
0.329 |
|
| 2010 |
Keyser RJ, Lesage S, Brice A, Carr J, Bardien S. Assessing the prevalence of PINK1 genetic variants in South African patients diagnosed with early- and late-onset Parkinson's disease Biochemical and Biophysical Research Communications. 398: 125-129. PMID 20558144 DOI: 10.1016/J.Bbrc.2010.06.049 |
0.549 |
|
| 2010 |
Bardien S, Marsberg A, Keyser R, Lombard D, Lesage S, Brice A, Carr J. LRRK2 G2019S mutation: Frequency and haplotype data in South African Parkinson's disease patients Journal of Neural Transmission. 117: 847-853. PMID 20544233 DOI: 10.1007/S00702-010-0423-6 |
0.525 |
|
| 2010 |
Lesage S, Patin E, Condroyer C, Leutenegger AL, Lohmann E, Giladi N, Bar-Shira A, Belarbi S, Hecham N, Pollak P, Ouvrard-Hernandez AM, Bardien S, Carr J, Benhassine T, Tomiyama H, et al. Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. Human Molecular Genetics. 19: 1998-2004. PMID 20197411 DOI: 10.1093/Hmg/Ddq081 |
0.51 |
|
| 2010 |
Lesage S, Condroyer C, Lohman E, Troiano A, Tison F, Viallet F, Damier P, Tranchant C, Vidhaillet M, Ouvrard-Hernandez AM, Dürr A, Brice A. Follow-up study of the GIGYF2 gene in French families with Parkinson's disease. Neurobiology of Aging. 31: 1069-71; discussion . PMID 20004041 DOI: 10.1016/J.Neurobiolaging.2009.06.008 |
0.53 |
|
| 2010 |
Evangelou E, Maraganore DM, Annesi G, Brighina L, Brice A, Elbaz A, Ferrarese C, Hadjigeorgiou GM, Krueger R, Lambert JC, Lesage S, Markopoulou K, Mellick GD, Meeus B, Pedersen NL, et al. Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: large-scale collaborative study. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 220-8. PMID 19475631 DOI: 10.1002/Ajmg.B.30980 |
0.409 |
|
| 2009 |
Pirkevi C, Lesage S, Brice A, BaÅŸak AN. From genes to proteins in mendelian Parkinson's disease: an overview. Anatomical Record (Hoboken, N.J. : 2007). 292: 1893-901. PMID 19943343 DOI: 10.1002/Ar.20968 |
0.502 |
|
| 2009 |
Sidransky E, Nalls MA, Aasly JO, Aharon-Peretz J, Annesi G, Barbosa ER, Bar-Shira A, Berg D, Bras J, Brice A, Chen CM, Clark LN, Condroyer C, De Marco EV, Dürr A, ... ... Lesage S, et al. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. The New England Journal of Medicine. 361: 1651-61. PMID 19846850 DOI: 10.1056/Nejmoa0901281 |
0.482 |
|
| 2009 |
Ribeiro MJ, Thobois S, Lohmann E, du Montcel ST, Lesage S, Pelissolo A, Dubois B, Mallet L, Pollak P, Agid Y, Broussolle E, Brice A, Remy P. A multitracer dopaminergic PET study of young-onset parkinsonian patients with and without parkin gene mutations. Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine. 50: 1244-50. PMID 19617340 DOI: 10.2967/Jnumed.109.063529 |
0.344 |
|
| 2009 |
Lesage S, Condroyer C, Lannuzel A, Lohmann E, Troiano A, Tison F, Damier P, Thobois S, Ouvrard-Hernandez AM, Rivaud-Péchoux S, Brefel-Courbon C, Destée A, Tranchant C, Romana M, Leclere L, et al. Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease. Journal of Medical Genetics. 46: 458-64. PMID 19357115 DOI: 10.1136/Jmg.2008.062612 |
0.491 |
|
| 2009 |
Lesage S, Brice A. Parkinson's disease: From monogenic forms to genetic susceptibility factors Human Molecular Genetics. 18. PMID 19297401 DOI: 10.1093/Hmg/Ddp012 |
0.552 |
|
| 2009 |
Pirkevi C, Lesage S, Condroyer C, Tomiyama H, Hattori N, Ertan S, Brice A, BaÅŸak AN. A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype. Neurogenetics. 10: 271-3. PMID 19172321 DOI: 10.1007/S10048-009-0173-5 |
0.5 |
|
| 2009 |
Ibáñez P, Lesage S, Janin S, Lohmann E, Durif F, Destée A, Bonnet AM, Brefel-Courbon C, Heath S, Zelenika D, Agid Y, Dürr A, Brice A. Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms. Archives of Neurology. 66: 102-8. PMID 19139307 DOI: 10.1001/Archneurol.2008.555 |
0.48 |
|
| 2009 |
Lohmann E, Thobois S, Lesage S, Broussolle E, du Montcel ST, Ribeiro MJ, Remy P, Pelissolo A, Dubois B, Mallet L, Pollak P, Agid Y, Brice A. A multidisciplinary study of patients with early-onset PD with and without parkin mutations. Neurology. 72: 110-6. PMID 18987353 DOI: 10.1212/01.Wnl.0000327098.86861.D4 |
0.495 |
|
| 2009 |
Lohmann E, Leclere L, De Anna F, Lesage S, Dubois B, Agid Y, Dürr A, Brice A. A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations. Parkinsonism & Related Disorders. 15: 273-6. PMID 18718805 DOI: 10.1016/J.Parkreldis.2008.06.008 |
0.521 |
|
| 2008 |
Lesage S, Belarbi S, Troiano A, Condroyer C, Hecham N, Pollak P, Lohman E, Benhassine T, Ysmail-Dahlouk F, Dürr A, Tazir M, Brice A. Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease? Neurology. 71: 1550-2. PMID 18981379 DOI: 10.1212/01.Wnl.0000338460.89796.06 |
0.503 |
|
| 2008 |
Milhavet F, Cuisset L, Hoffman HM, Slim R, El-Shanti H, Aksentijevich I, Lesage S, Waterham H, Wise C, Sarrauste de Menthiere C, Touitou I. The infevers autoinflammatory mutation online registry: update with new genes and functions. Human Mutation. 29: 803-8. PMID 18409191 DOI: 10.1002/Humu.20720 |
0.389 |
|
| 2008 |
Lesage S, Lohmann E, Tison F, Durif F, Dürr A, Brice A. Gene symbol: PARK2. Disease: Parkinsonism, juvenile, autosomal recessive. Human Genetics. 123: 114. PMID 18386383 |
0.347 |
|
| 2008 |
Lohmann E, Welter ML, Fraix V, Krack P, Lesage S, Laine S, Tanguy ML, Houeto JL, Mesnage V, Pollak P, Durr A, Agid Y, Brice A. Are parkin patients particularly suited for deep-brain stimulation? Movement Disorders : Official Journal of the Movement Disorder Society. 23: 740-3. PMID 18228569 DOI: 10.1002/Mds.21903 |
0.415 |
|
| 2008 |
Lesage S, Lohmann E, Tison F, Durif F, Dürr A, Brice A. Rare heterozygous parkin variants in French early-onset Parkinson disease patients and controls Journal of Medical Genetics. 45: 43-46. PMID 17766365 DOI: 10.1136/Jmg.2007.051854 |
0.533 |
|
| 2007 |
Lesage S, Leclere L, Lohmann E, Borg M, Ruberg M, Dürr A, Brice A, Agid Y, Bonnet AM, Broussolle E, Damier P, Destée A, Durif F, Martinez M, Penet C, et al. Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease Neurodegenerative Diseases. 4: 195-198. PMID 17596714 DOI: 10.1159/000101844 |
0.53 |
|
| 2007 |
Charles P, Camuzat A, Benammar N, Sellal F, Destée A, Bonnet AM, Lesage S, Le Ber I, Stevanin G, Dürr A, Brice A, Agid Y, Borg M, Broussolle E, Damier P, et al. Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism? Neurology. 69: 1970-1975. PMID 17568014 DOI: 10.1212/01.Wnl.0000269323.21969.Db |
0.484 |
|
| 2007 |
Clark LN, Haamer E, Mejia-Santana H, Harris J, Lesage S, Durr A, Bs SJ, Hedrich K, Louis ED, Cote LJ, Andrews H, Fahn S, Waters C, Ford B, Frucht S, et al. Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 932-7. PMID 17415800 DOI: 10.1002/Mds.21419 |
0.562 |
|
| 2007 |
Lesage S, Janin S, Lohmann E, Leutenegger AL, Leclere L, Viallet F, Pollak P, Durif F, Thobois S, Layet V, Vidailhet M, Agid Y, Dürr A, Brice A, et al. LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans. Archives of Neurology. 64: 425-30. PMID 17353388 DOI: 10.1001/Archneur.64.3.425 |
0.539 |
|
| 2007 |
Grünewald A, Breedveld GJ, Lohmann-Hedrich K, Rohé CF, König IR, Hagenah J, Vanacore N, Meco G, Antonini A, Goldwurm S, Lesage S, Dürr A, Binkofski F, Siebner H, Münchau A, et al. Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis. Neurogenetics. 8: 103-9. PMID 17219214 DOI: 10.1007/S10048-006-0072-Y |
0.403 |
|
| 2007 |
Schüpbach M, Lohmann E, Anheim M, Lesage S, Czernecki V, Yaici S, Worbe Y, Charles P, Welter ML, Pollak P, Dürr A, Agid Y, Brice A. Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutations. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 119-22. PMID 17080443 DOI: 10.1002/Mds.21178 |
0.467 |
|
| 2007 |
Lesage S, Magali P, Lohmann E, Lacomblez L, Teive H, Janin S, Cousin PY, Dürr A, Brice A, Agid Y, Bonnet AM, Borg M, Broussolle E, Damier P, Destée A, et al. Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism Human Mutation. 28: 27-32. PMID 17068781 DOI: 10.1002/Humu.20436 |
0.448 |
|
| 2007 |
Lesage S, Dürr A, Brice A. LRRK2: a link between familial and sporadic Parkinson's disease? Pathologie Biologie. 55: 107-110. PMID 16884863 DOI: 10.1016/J.Patbio.2006.06.001 |
0.432 |
|
| 2006 |
Leutenegger AL, Salih MA, Ibáñez P, Mukhtar MM, Lesage S, Arabi A, Lohmann E, Dürr A, Ahmed AE, Brice A. Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1. Archives of Neurology. 63: 1257-61. PMID 16966503 DOI: 10.1001/Archneur.63.9.1257 |
0.467 |
|
| 2006 |
Ishihara L, Warren L, Gibson R, Amouri R, Lesage S, Dürr A, Tazir M, Wszolek ZK, Uitti RJ, Nichols WC, Griffith A, Hattori N, Leppert D, Watts R, Zabetian CP, et al. Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations. Archives of Neurology. 63: 1250-4. PMID 16966502 DOI: 10.1001/Archneur.63.9.1250 |
0.527 |
|
| 2006 |
Pineda-Trujillo N, Apergi M, Moreno S, Arias W, Lesage S, Franco A, Sepulveda-Falla D, Cano D, Buriticá O, Pineda D, Uribe CS, de Yebenes JG, Lees AJ, Brice A, Bedoya G, et al. A genetic cluster of early onset Parkinson's disease in a Colombian population. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 141: 885-9. PMID 16941654 DOI: 10.1002/Ajmg.B.30375 |
0.49 |
|
| 2006 |
Lesage S, Dürr A, Tazir M, Lohmann E, Leutenegger AL, Janin S, Pollak P, Brice A. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs [13] New England Journal of Medicine. 354: 422-423. PMID 16436781 DOI: 10.1056/Nejmc055540 |
0.396 |
|
| 2006 |
Ibáñez P, Lesage S, Lohmann E, Thobois S, De Michele G, Borg M, Agid Y, Dürr A, Brice A. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain : a Journal of Neurology. 129: 686-94. PMID 16401616 DOI: 10.1093/Brain/Awl005 |
0.513 |
|
| 2005 |
Lesage S, Ibanez P, Lohmann E, Pollak P, Tison F, Tazir M, Leutenegger AL, Guimaraes J, Bonnet AM, Agid Y, Dürr A, Brice A. G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Annals of Neurology. 58: 784-7. PMID 16240353 DOI: 10.1002/Ana.20636 |
0.534 |
|
| 2005 |
Lesage S, Leutenegger AL, Ibanez P, Janin S, Lohmann E, Dürr A, Brice A. LRRK2 haplotype analyses in European and North African families with Parkinson disease: A common founder for the G2019S mutation dating from the 13th century [2] American Journal of Human Genetics. 77: 330-332. PMID 16145815 DOI: 10.1086/432422 |
0.466 |
|
| 2005 |
Lesage S, Ibanez P, Lohmann E, Agid Y, Dürr A, Brice A. The G2019SLRRK2 Mutation in Autosomal Dominant European and North African Parkinson’s Disease is Frequent and its Penetrance is Age-Dependant LBS.003 Neurology. 64: 1826-1826. DOI: 10.1212/Wnl.64.10.1826-B |
0.316 |
|
| 2004 |
Touitou I, Lesage S, McDermott M, Cuisset L, Hoffman H, Dode C, Shoham N, Aganna E, Hugot JP, Wise C, Waterham H, Pugnere D, Demaille J, Sarrauste de Menthiere C. Infevers: an evolving mutation database for auto-inflammatory syndromes. Human Mutation. 24: 194-8. PMID 15300846 DOI: 10.1002/Humu.20080 |
0.373 |
|
| 2004 |
Miceli-Richard C, Zouali H, Said-Nahal R, Lesage S, Merlin F, De Toma C, Blanche H, Sahbatou M, Dougados M, Thomas G, Breban M, Hugot JP. Significant linkage to spondyloarthropathy on 9q31-34. Human Molecular Genetics. 13: 1641-8. PMID 15234954 DOI: 10.1093/Hmg/Ddh179 |
0.342 |
|
| 2003 |
Hugot JP, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, Montague S, Gassull M, Christensen S, Finkel Y, Gower-Rousseau C, Modigliani R, Zouali H, Lesage S, Chamaillard M, et al. Clustering of Crohn's disease within affected sibships. European Journal of Human Genetics : Ejhg. 11: 179-84. PMID 12634866 DOI: 10.1038/Sj.Ejhg.5200932 |
0.364 |
|
| 2003 |
Chamaillard M, Philpott D, Girardin SE, Zouali H, Lesage S, Chareyre F, Bui TH, Giovannini M, Zaehringer U, Penard-Lacronique V, Sansonetti PJ, Hugot JP, Thomas G. Gene-environment interaction modulated by allelic heterogeneity in inflammatory diseases. Proceedings of the National Academy of Sciences of the United States of America. 100: 3455-60. PMID 12626759 DOI: 10.1073/Pnas.0530276100 |
0.318 |
|
| 2003 |
Zouali H, Lesage S, Merlin F, Cezard J, Colombel J, Belaiche J, Almer S, Tysk C, O'Morain C, Gassull M, Christensen S, Finkel Y, Modigliani R, Gower-Rousseau C, Macry J, et al. CARD4/NOD1 is not involved in inflammatory bowel disease Gut. 52: 71-74. PMID 12477763 DOI: 10.1136/Gut.52.1.71 |
0.39 |
|
| 2002 |
Lesage S, Zouali H, Cézard JP, Colombel JF, Belaiche J, Almer S, Tysk C, O'Morain C, Gassull M, Binder V, Finkel Y, Modigliani R, Gower-Rousseau C, Macry J, Merlin F, et al. CARD15/NOD2 mutational analysis and genotype-phenotype correlation in 612 patients with inflammatory bowel disease. American Journal of Human Genetics. 70: 845-57. PMID 11875755 DOI: 10.1086/339432 |
0.431 |
|
| 2001 |
Miceli-Richard C, Lesage S, Rybojad M, Prieur AM, Manouvrier-Hanu S, Häfner R, Chamaillard M, Zouali H, Thomas G, Hugot JP. CARD15 mutations in Blau syndrome. Nature Genetics. 29: 19-20. PMID 11528384 DOI: 10.1038/Ng720 |
0.417 |
|
| 2001 |
Hugot JP, Chamaillard M, Zouali H, Lesage S, Cézard JP, Belaiche J, Almer S, Tysk C, O'morain CA, Gassull M, Binder V, Finkel Y, Cortot A, Modigliani R, Laurent-Puig P, et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease Nature. 411: 599-603. PMID 11385576 DOI: 10.1038/35079107 |
0.379 |
|
| 2000 |
Lesage S, Zouali H, Colombel JF, Belaiche J, Cézard JP, Tysk C, Almer S, Gassull M, Binder V, Chamaillard M, Gall IL, Thomas G, Hugot JP. Genetic analyses of chromosome 12 loci in Crohn's disease. Gut. 47: 787-791. PMID 11076876 DOI: 10.1136/Gut.47.6.787 |
0.415 |
|
| 1999 |
Hugot JP, Zouali H, Lesage S, Thomas G. Etiology of the inflammatory bowel diseases. International Journal of Colorectal Disease. 14: 2-9. PMID 10207723 DOI: 10.1007/S003840050175 |
0.36 |
|
| 1997 |
Lesage S, Velho G, Vionnet N, Chatelain N, Demenais F, Passa P, Soubrier F, Froguel P. Genetic studies of the renin-angiotensin system in arterial hypertension associated with non-insulin-dependent diabetes mellitus Journal of Hypertension. 15: 601-606. PMID 9218178 DOI: 10.1097/00004872-199715060-00005 |
0.406 |
|
| 1997 |
Vionnet N, Hani EH, Lesage S, Philippi A, Hager J, Varret M, Stoffel M, Tanizawa Y, Chiu KC, Glaser B, Permutt MA, Passa P, Demenais F, Froguel P. Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs. Diabetes. 46: 1062-8. PMID 9166680 DOI: 10.2337/Diab.46.6.1062 |
0.722 |
|
| 1995 |
Lesage S, Hani EH, Philippi A, Vaxillaire M, Hager J, Passa P, Demenais F, Froguel P, Vionnet N. Rapid publication: Linkage analyses of the MODY3 locus on chromosome 12q with late-onset NIDDM Diabetes. 44: 1243-1247. PMID 7556965 DOI: 10.2337/Diab.44.10.1243 |
0.726 |
|
| 1993 |
Froguel P, Zouali H, Vionnet N, Velho G, Vaxillaire M, Sun F, Lesage S, Stoffel M, Takeda J, Passa P. Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus. The New England Journal of Medicine. 328: 697-702. PMID 8433729 DOI: 10.1056/NEJM199303113281005 |
0.47 |
|
| 1993 |
Sun F, Knebelmann B, Pueyo ME, Zouali H, Lesage S, Vaxillaire M, Passa P, Cohen D, Velho G, Antignac C. Deletion of the donor splice site of intron 4 in the glucokinase gene causes maturity-onset diabetes of the young. Journal of Clinical Investigation. 92: 1174-1180. PMID 8376578 DOI: 10.1172/Jci116687 |
0.38 |
|
| 1993 |
Zouali H, Vaxillaire M, Lesage S, Sun F, Velho G, Vionnet N, Chiu K, Passa P, Permutt A, Demenais F, Cohen D, Beckmann J, Froguel P. Linkage Analysis and Molecular Scanning of Glucokinase Gene in NIDDM Families Diabetes. 42: 1238-1245. PMID 8349034 DOI: 10.2337/Diab.42.9.1238 |
0.532 |
|
| 1992 |
Vionnet N, Stoffel M, Takeda J, Yasuda K, Bell GI, Zouali H, Lesage S, Velho G, Iris F, Passa P. Nonsense mutation in the glucokinase gene causes early-onset non-insulin-dependent diabetes mellitus. Nature. 356: 721-2. PMID 1570017 DOI: 10.1038/356721A0 |
0.44 |
|
| 1992 |
Froguel P, Vaxillaire M, Sun F, Velho G, Zouali H, Butel MO, Lesage S, Vionnet N, Clément K, Fougerousse F, Tanizawa Y, Weissenbach J, Beckmann JS, Lathrop GM, Passa P, et al. Close Linkage of Glucokinase Locus on Chromosome 7p to Early-Onset Non-Insulin-Dependent Diabetes Mellitus Nature. 356: 162-164. PMID 1545870 DOI: 10.1038/356162A0 |
0.521 |
|
| 1992 |
Stoffel M, Froguel P, Takeda J, Zouali H, Vionnet N, Nishi S, Weber IT, Harrison RW, Pilkis SJ, Lesage S. Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus. Proceedings of the National Academy of Sciences of the United States of America. 89: 7698-702. PMID 1502186 DOI: 10.1073/Pnas.89.16.7698 |
0.477 |
|
| 1992 |
Froguel P, Vaxillaire M, Sun F, Velho G, Zouali H, Butel MO, Lesage S, Vionnet N, Clément K, Fougerousse F, Tanizawa Y, Weissenbach J, Beckmann JS, Lathrop GM, Passa P, et al. Erratum: Close linkage of glucokinase locus on chromosome 7p to early-onset non-insulin-dependent diabetes mellitus (Nature (1992) 356 (162-164)) Nature. 357. DOI: 10.1038/357607C0 |
0.461 |
|
| 1991 |
Froguel P, Vionnet N, Lesage S, Velho G, Cohen D. Two Taql RFLPs at the GLUT2 locus in French caucasian population Nucleic Acids Research. 19: 5799. PMID 1682886 DOI: 10.1093/Nar/19.20.5799 |
0.335 |
|
| Show low-probability matches. |