Articles with public access mandates - Maithe TauberLearn more
Not available anywhere: 7
Review
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk
N Bouatia-Naji, A Bonnefond, C Cavalcanti-Proença, T Sparsø, ...
Nature genetics 41 (1), 89-94, 2009
Mandates: Genome Canada, National Institute of Health and Medical Research, France
Review
An early postnatal oxytocin treatment prevents social and learning deficits in adult mice deficient for Magel2, a gene involved in Prader-Willi syndrome and autism
H Meziane, F Schaller, S Bauer, C Villard, V Matarazzo, F Riet, G Guillon, ...
Biological psychiatry 78 (2), 85-94, 2015
Mandates: European Commission
Review
CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome
F Brioude, I Oliver-Petit, A Blaise, F Praz, S Rossignol, M Le Jule, ...
Journal of medical genetics 50 (12), 823-830, 2013
Mandates: National Institute of Health and Medical Research, France
Review
SHP2 drives inflammation-triggered insulin resistance by reshaping tissue macrophage populations
R Paccoud, C Saint-Laurent, E Piccolo, M Tajan, A Dortignac, O Pereira, ...
Science Translational Medicine 13 (591), eabe2587, 2021
Mandates: National Institute of Health and Medical Research, France, European …
Review
Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: identification a cryptic donor splice site in the exon 19
HM Targovnik, T Edouard, V Varela, M Tauber, CE Citterio, ...
Molecular and cellular endocrinology 348 (1), 313-321, 2012
Mandates: Government of Spain
Review
Imprinting disorders
T Eggermann, D Monk, GP de Nanclares, M Kagami, E Giabicani, ...
Nature Reviews Disease Primers 9 (1), 33, 2023
Mandates: German Research Foundation, National Institute for Health Research, UK …
Review
Setmelanotide for controlling weight and hunger in Bardet-Biedl syndrome
M Tauber
The Lancet Diabetes & Endocrinology 10 (12), 829-830, 2022
Mandates: European Commission
Available somewhere: 27
Review
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
Mandates: Genome Canada, German Research Foundation
Review
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations
D Meyre, J Delplanque, JC Chèvre, C Lecoeur, S Lobbens, S Gallina, ...
Nature genetics 41 (2), 157-159, 2009
Mandates: Genome Canada, German Research Foundation
Review
Growth Hormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome
CL Deal, M Tony, C Höybye, DB Allen, M Tauber, JS Christiansen, ...
The Journal of Clinical Endocrinology & Metabolism 98 (6), E1072-E1087, 2013
Mandates: US National Institutes of Health, National Institute of Health and Medical …
Review
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ...
Human genetics 131, 565-579, 2012
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome
LC Burnett, CA LeDuc, CR Sulsona, D Paull, R Rausch, S Eddiry, ...
The Journal of clinical investigation 127 (1), 293-305, 2017
Mandates: US National Institutes of Health
Review
Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesity
JWM Creemers, H Choquet, P Stijnen, V Vatin, M Pigeyre, S Beckers, ...
Diabetes 61 (2), 383-390, 2012
Mandates: Research Foundation (Flanders), German Research Foundation, National …
Review
Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature
ADR Serra-Nédélec, T Edouard, K Tréguer, M Tajan, T Araki, M Dance, ...
Proceedings of the National Academy of Sciences 109 (11), 4257-4262, 2012
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
Review
Ontogenesis of oxytocin pathways in the mammalian brain: late maturation and psychosocial disorders
V Grinevich, MG Desarménien, B Chini, M Tauber, F Muscatelli
Frontiers in neuroanatomy 8, 164, 2015
Mandates: German Research Foundation, National Institute of Health and Medical …
Review
Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia
SB Heymsfield, NM Avena, L Baier, P Brantley, GA Bray, LC Burnett, ...
Obesity 22 (S1), S1-S17, 2014
Mandates: US National Institutes of Health
Review
Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension
M Baron, J Maillet, M Huyvaert, A Dechaume, R Boutry, H Loiselle, ...
Nature medicine 25 (11), 1733-1738, 2019
Mandates: National Institute of Health and Medical Research, France, European …
Review
LEOPARD syndrome-associated SHP2 mutation confers leanness and protection from diet-induced obesity
M Tajan, A Batut, T Cadoudal, S Deleruyelle, S Le Gonidec, ...
Proceedings of the National Academy of Sciences 111 (42), E4494-E4503, 2014
Mandates: National Institute of Health and Medical Research, France
Review
Hypothalamic syndrome
HL Müller, M Tauber, EA Lawson, J Özyurt, B Bison, JP Martinez-Barbera, ...
Nature reviews Disease primers 8 (1), 24, 2022
Mandates: Cancer Research UK, UK Medical Research Council, Brain Tumour Charity, UK
Review
Chromosome 14q32. 2 imprinted region disruption as an alternative molecular diagnosis of Silver-Russell syndrome
S Geoffron, W Abi Habib, S Chantot-Bastaraud, B Dubern, V Steunou, ...
The Journal of Clinical Endocrinology & Metabolism 103 (7), 2436-2446, 2018
Mandates: National Institute of Health and Medical Research, France, European Commission
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