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Hans Markus Münter
Hans Markus Münter
5 Prime Sciences Inc.
Adresse e-mail validée de 5primesciences.com - Page d'accueil
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BMP and Ihh/PTHrP signaling interact to coordinate chondrocyte proliferation and differentiation
E Minina, HM Wenzel, C Kreschel, S Karp, W Gaffield, AP McMahon, ...
Development 128 (22), 4523-4534, 2001
5942001
Contribution to Alzheimer's disease risk of rare variants in TREM2, SORL1, and ABCA7 in 1779 cases and 1273 controls
C Bellenguez, C Charbonnier, B Grenier-Boley, O Quenez, K Le Guennec, ...
Neurobiology of aging 59, 220. e1-220. e9, 2017
1602017
SORL1 rare variants: a major risk factor for familial early-onset Alzheimer’s disease
G Nicolas, C Charbonnier, D Wallon, O Quenez, C Bellenguez, ...
Molecular psychiatry 21 (6), 831-836, 2016
1332016
Inactivation of anoctamin‐6/Tmem16f, a regulator of phosphatidylserine scrambling in osteoblasts, leads to decreased mineral deposition in skeletal tissues
HWA Ehlen, M Chinenkova, M Moser, HM Munter, Y Krause, S Gross, ...
Journal of Bone and Mineral Research 28 (2), 246-259, 2013
1232013
Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome
N Lahrouchi, R Tadros, L Crotti, Y Mizusawa, PG Postema, L Beekman, ...
Circulation 142 (4), 324-338, 2020
1072020
Screening of dementia genes by whole-exome sequencing in early-onset Alzheimer disease: input and lessons
G Nicolas, D Wallon, C Charbonnier, O Quenez, S Rousseau, AC Richard, ...
European Journal of Human Genetics 24 (5), 710-716, 2016
1002016
ABCA7 rare variants and Alzheimer disease risk
K Le Guennec, G Nicolas, O Quenez, C Charbonnier, D Wallon, ...
Neurology 86 (23), 2134-2137, 2016
792016
17q21. 31 duplication causes prominent tau-related dementia with increased MAPT expression
K Le Guennec, O Quenez, G Nicolas, D Wallon, S Rousseau, AC Richard, ...
Molecular Psychiatry 22 (8), 1119-1125, 2017
702017
Don’t ignore genetic data from minority populations
SG Chief Ben-Eghan, Rosie Sun, Jose Sergio Hleap, Alex Diaz-Papkovich, Hans ...
Nature 585, 184-186, 2020
502020
Association of FADS1/2 locus variants and polyunsaturated fatty acids with aortic stenosis
HY Chen, BJ Cairns, AM Small, HA Burr, A Ambikkumar, A Martinsson, ...
JAMA cardiology 5 (6), 694-702, 2020
382020
Proteome-wide Mendelian randomization implicates nephronectin as an actionable mediator of the effect of obesity on COVID-19 severity
S Yoshiji, G Butler-Laporte, T Lu, JDS Willett, CY Su, T Nakanishi, ...
Nature Metabolism 5 (2), 248-264, 2023
252023
NK cell recruitment limits tissue damage during an enteric helminth infection
ME Gentile, Y Li, A Robertson, K Shah, G Fontes, E Kaufmann, B Polese, ...
Mucosal Immunology 13 (2), 357-370, 2020
242020
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
H Yu Chen, C Dina, AM Small, CM Shaffer, RT Levinson, A Helgadóttir, ...
European heart journal 44 (21), 1927-1939, 2023
212023
Common genetic variants contribute to risk of transposition of the great arteries
D Škorić-Milosavljević, R Tadros, FM Bosada, F Tessadori, JH Van Weerd, ...
Circulation research 130 (2), 166-180, 2022
162022
Multi-ethnic GWAS and meta-analysis of sleep quality identify MPP6 as a novel gene that functions in sleep center neurons
S Khoury, QP Wang, M Parisien, P Gris, AV Bortsov, SD Linnstaedt, ...
Sleep 44 (3), zsaa211, 2021
102021
East Asian-specific and cross-ancestry genome-wide meta-analyses provide mechanistic insights into peptic ulcer disease
Y He, M Koido, Y Sutoh, M Shi, Y Otsuka-Yamasaki, HM Munter, ...
Nature Genetics 55 (12), 2129-2138, 2023
32023
Identifizierung neuer Zielgene im Indian-Hedgehog Signalweg
HM Wenzel
12003
Fine-mapping, signal-colocalization and quantitative trait locus causal analysis of the chr17q12-21 asthma locus, implicates basal lymphocytes and eosinophil levels
C Ben-Eghan, A Diaz-Papkovich, M Munter, C Terao, S Gravel, M Lathrop, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 793-794, 2024
2024
Characterizing the inaccurate quality metric in genotype imputation using the TOPMed reference panel
M Shi, M Koido, Y Kamatani, C Tanikawa, K Matsuda, C Terao, M Lathrop, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 32, 680-681, 2024
2024
Loss of the APP regulator RHBDL4 preserves memory in an Alzheimer′ s disease mouse model.
YCM Penalva, S Paschkowsky, J Yang, SJ Recinto, J Cinkorpumin, ...
bioRxiv, 2024.02. 22.579698, 2024
2024
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