| Year |
Citation |
Score |
| 2015 |
Philippe J, Stijnen P, Meyre D, De Graeve F, Thuillier D, Delplanque J, Gyapay G, Sand O, Creemers JW, Froguel P, Bonnefond A. A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity. International Journal of Obesity (2005). 39: 295-302. PMID 24890885 DOI: 10.1038/Ijo.2014.96 |
0.678 |
|
| 2014 |
Perimenis P, Bouckenooghe T, Delplanque J, Moitrot E, Eury E, Lobbens S, Gosset P, Devisme L, Duvillie B, Abderrahmani A, Storme L, Fontaine P, Froguel P, Vambergue A. Placental antiangiogenic prolactin fragments are increased in human and rat maternal diabetes. Biochimica Et Biophysica Acta. 1842: 1783-93. PMID 24984282 DOI: 10.1016/J.Bbadis.2014.06.026 |
0.653 |
|
| 2012 |
Bonnefond A, Philippe J, Durand E, Dechaume A, Huyvaert M, Montagne L, Marre M, Balkau B, Fajardy I, Vambergue A, Vatin V, Delplanque J, Le Guilcher D, De Graeve F, Lecoeur C, et al. Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene. Plos One. 7: e37423. PMID 22701567 DOI: 10.1371/Journal.Pone.0037423 |
0.691 |
|
| 2012 |
Dastani Z, Hivert MF, Timpson N, Perry JR, Yuan X, Scott RA, Henneman P, Heid IM, Kizer JR, Lyytikäinen LP, Fuchsberger C, Tanaka T, Morris AP, Small K, Isaacs A, ... ... Delplanque J, et al. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. Plos Genetics. 8: e1002607. PMID 22479202 DOI: 10.1371/Journal.Pgen.1002607 |
0.556 |
|
| 2012 |
Palmer ND, McDonough CW, Hicks PJ, Roh BH, Wing MR, An SS, Hester JM, Cooke JN, Bostrom MA, Rudock ME, Talbert ME, Lewis JP, Ferrara A, ... ... Delplanque J, et al. A genome-wide association search for type 2 diabetes genes in African Americans. Plos One. 7: e29202. PMID 22238593 DOI: 10.1371/Journal.Pone.0029202 |
0.564 |
|
| 2012 |
Rouskas K, Kouvatsi A, Paletas K, Papazoglou D, Tsapas A, Lobbens S, Vatin V, Durand E, Labrune Y, Delplanque J, Meyre D, Froguel P. Common variants in FTO, MC4R, TMEM18, PRL, AIF1, and PCSK1 show evidence of association with adult obesity in the greek population Obesity. 20: 389-395. PMID 21720444 DOI: 10.1038/Oby.2011.177 |
0.594 |
|
| 2012 |
Perimenis P, Bouckenooghe T, Eury E, Lobbens S, Delplanque J, Moitrot E, Gosset P, Sisino G, Storme L, Froguel P, Vambergue A. O67 L’analyse du transcriptome montre une dysfonction foeto-placentaire au cours du diabète maternel Diabetes & Metabolism. 38: A17. DOI: 10.1016/S1262-3636(12)71045-5 |
0.426 |
|
| 2012 |
Perimenis P, Bouckenooghe T, Eury E, Lobbens S, Delplanque J, Moitrot E, Gosset P, Sisino G, Storme L, Fontaine P, Froguel P, Vambergue A. Augmentation de l’expression de la prolactine placentaire dans un modèle de rate gestante diabétique Annales D'Endocrinologie. 73: 251. DOI: 10.1016/J.Ando.2012.07.067 |
0.365 |
|
| 2010 |
Bonnefond A, Durand E, Sand O, De Graeve F, Gallina S, Busiah K, Lobbens S, Simon A, Bellanné-Chantelot C, Létourneau L, Scharfmann R, Delplanque J, Sladek R, Polak M, Vaxillaire M, et al. Molecular diagnosis of neonatal diabetes mellitus using next-generation sequencing of the whole exome. Plos One. 5: e13630. PMID 21049026 DOI: 10.1371/Journal.Pone.0013630 |
0.468 |
|
| 2010 |
Scherag A, Dina C, Hinney A, Vatin V, Scherag S, Vogel CI, Müller TD, Grallert H, Wichmann HE, Balkau B, Heude B, Jarvelin MR, Hartikainen AL, Levy-Marchal C, Weill J, ... Delplanque J, et al. Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups. Plos Genetics. 6: e1000916. PMID 20421936 DOI: 10.1371/Journal.Pgen.1000916 |
0.581 |
|
| 2010 |
Dupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL, Bouatia-Naji N, Gloyn AL, Lindgren CM, Mägi R, Morris AP, Randall J, Johnson T, ... ... Delplanque J, et al. New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nature Genetics. 42: 105-16. PMID 20081858 DOI: 10.1038/Ng.520 |
0.526 |
|
| 2010 |
Saxena R, Hivert MF, Langenberg C, Tanaka T, Pankow JS, Vollenweider P, Lyssenko V, Bouatia-Naji N, Dupuis J, Jackson AU, Kao WH, Li M, Glazer NL, Manning AK, Luan J, ... ... Delplanque J, et al. Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nature Genetics. 42: 142-8. PMID 20081857 DOI: 10.1038/Ng.521 |
0.531 |
|
| 2010 |
Repapi E, Sayers I, Wain LV, Burton PR, Johnson T, Obeidat M, Zhao JH, Ramasamy A, Zhai G, Vitart V, Huffman JE, Igl W, Albrecht E, Deloukas P, Henderson J, ... ... Delplanque J, et al. Genome-wide association study identifies five loci associated with lung function. Nature Genetics. 42: 36-44. PMID 20010834 DOI: 10.1038/Ng.501 |
0.468 |
|
| 2010 |
Dupuis J, Langenberg C, Prokopenko I, Saxena R, Soranzo N, Jackson AU, Wheeler E, Glazer NL, Bouatia-Naji N, Gloyn AL, Lindgren CM, Mägi R, Morris AP, Randall J, Johnson T, ... ... Delplanque J, et al. Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk Nature Genetics. 42: 464-464. DOI: 10.1038/Ng0510-464A |
0.508 |
|
| 2010 |
Vaxillaire M, Busiah K, Bonnefond A, Lecoeur C, Dechaume A, Simon A, Graeve Fd, Gallina S, Delplanque J, Cavé H, Polak M, Froguel P. P210 Nouvelles Approches dans l’Étude des Diabètes Monogéniques chez l’Enfant et l’Adulte Jeune, et Distribution des Étiologies Génétiques à partir de la Cohorte du Réseau d’Étude Français Diabetes & Metabolism. 36. DOI: 10.1016/S1262-3636(10)70358-X |
0.425 |
|
| 2010 |
Cauchi S, Lobbens S, Graeve Fd, Delplanque J, Achhab YE, Chikri M, Froguel P. P208 Quels Sont Les Facteurs Génétiques Associés Au Diabète De Type 2 Chez Les Marocains Diabetes & Metabolism. 36. DOI: 10.1016/S1262-3636(10)70356-6 |
0.411 |
|
| 2009 |
Blakemore AIF, Meyre D, Delplanque J, Vatin V, Lecoeur C, Marre M, Tichet J, Balkau B, Froguel P, Walley AJ. A rare variant in the visfatin gene (nampt/pbef1) is associated with protection from obesity Obesity. 17: 1549-1553. PMID 19300429 DOI: 10.1038/Oby.2009.75 |
0.611 |
|
| 2009 |
Meyre D, Delplanque J, Chèvre JC, Lecoeur C, Lobbens S, Gallina S, Durand E, Vatin V, Degraeve F, Proença C, Gaget S, Körner A, Kovacs P, Kiess W, Tichet J, et al. Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. Nature Genetics. 41: 157-9. PMID 19151714 DOI: 10.1038/Ng.301 |
0.589 |
|
| 2009 |
Bouatia-Naji N, Bonnefond A, Cavalcanti-Proença C, Sparsø T, Holmkvist J, Marchand M, Delplanque J, Lobbens S, Rocheleau G, Durand E, De Graeve F, Chèvre JC, Borch-Johnsen K, Hartikainen AL, Ruokonen A, et al. A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk. Nature Genetics. 41: 89-94. PMID 19060909 DOI: 10.1038/Ng.277 |
0.711 |
|
| 2009 |
El Achhab Y, Meyre D, Bouatia-Naji N, Berraho M, Deweirder M, Vatin V, Delplanque J, Serhier Z, Lyoussi B, Nejjari C, Froguel P, Chikri M. Association of the ENPP1 K121Q polymorphism with type 2 diabetes and obesity in the Moroccan population Diabetes and Metabolism. 35: 37-42. PMID 19046915 DOI: 10.1016/J.Diabet.2008.06.005 |
0.629 |
|
| 2008 |
Durand E, Lecoeur C, Delplanque J, Benzinou M, Degraeve F, Boutin P, Marre M, Balkau B, Charpentier G, Froguel P, Meyre D. Evaluating the association of FAAH common gene variation with childhood, adult severe obesity and type 2 diabetes in the French population Obesity Facts. 1: 305-309. PMID 20054193 DOI: 10.1159/000178157 |
0.624 |
|
| 2008 |
Cauchi S, Meyre D, Durand E, Proença C, Marre M, Hadjadj S, Choquet H, De Graeve F, Gaget S, Allegaert F, Delplanque J, Permutt MA, Wasson J, Blech I, Charpentier G, et al. Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value Plos One. 3. PMID 18461161 DOI: 10.1371/Journal.Pone.0002031 |
0.579 |
|
| 2008 |
Benzinou M, Chèvre JC, Ward KJ, Lecoeur C, Dina C, Lobbens S, Durand E, Delplanque J, Horber FF, Heude B, Balkau B, Borch-johnsen K, Jørgensen T, Hansen T, Pedersen O, et al. Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations Human Molecular Genetics. 17: 1916-1921. PMID 18375449 DOI: 10.1093/Hmg/Ddn089 |
0.721 |
|
| 2008 |
Liu YJ, Liu XG, Wang L, Dina C, Yan H, Liu JF, Levy S, Papasian CJ, Drees BM, Hamilton JJ, Meyre D, Delplanque J, Pei YF, Zhang L, Recker RR, et al. Genome-wide association scans identified CTNNBL1 as a novel gene for obesity. Human Molecular Genetics. 17: 1803-13. PMID 18325910 DOI: 10.1093/Hmg/Ddn072 |
0.612 |
|
| 2008 |
Meyre D, Farge M, Lecoeur C, Proenca C, Durand E, Allegaert F, Tichet J, Marre M, Balkau B, Weill J, Delplanque J, Froguel P. R125W coding variant in TBC1D1 confers risk for familial obesity and contributes to linkage on chromosome 4p14 in the French population Human Molecular Genetics. 17: 1798-1802. PMID 18325908 DOI: 10.1093/Hmg/Ddn070 |
0.534 |
|
| 2008 |
Mirhashemi F, Kluth O, Scherneck S, Vogel H, Kluge R, Schürmann A, Joost H, Neschen S, McDoniel SO, Nelson HA, Thomson CA, Durand E, Lecoeur C, Delplanque J, Benzinou M, et al. Contents Vol. 1, 2008 Obesity Facts. 1. DOI: 10.1159/000192785 |
0.351 |
|
| 2008 |
Mirhashemi F, Kluth O, Scherneck S, Vogel H, Kluge R, Schürmann A, Joost H, Neschen S, McDoniel SO, Nelson HA, Thomson CA, Durand E, Lecoeur C, Delplanque J, Benzinou M, et al. Subject Index Vol. 1, 2008 Obesity Facts. 1: 342-342. DOI: 10.1159/000192783 |
0.402 |
|
| 2008 |
Mirhashemi F, Kluth O, Scherneck S, Vogel H, Kluge R, Schürmann A, Joost H, Neschen S, McDoniel SO, Nelson HA, Thomson CA, Durand E, Lecoeur C, Delplanque J, Benzinou M, et al. Acknowledgement to Revierwers Obesity Facts. 1: 339-339. DOI: 10.1159/000192780 |
0.355 |
|
| 2008 |
Mirhashemi F, Kluth O, Scherneck S, Vogel H, Kluge R, Schürmann A, Joost H, Neschen S, McDoniel SO, Nelson HA, Thomson CA, Durand E, Lecoeur C, Delplanque J, Benzinou M, et al. Meetings and Conferences Obesity Facts. 1: 117-118. DOI: 10.1159/000119750 |
0.386 |
|
| 2007 |
Salonen JT, Uimari P, Aalto JM, Pirskanen M, Kaikkonen J, Todorova B, Hyppönen J, Korhonen VP, Asikainen J, Devine C, Tuomainen TP, Luedemann J, Nauck M, Kerner W, Stephens RH, ... ... Delplanque J, et al. Type 2 diabetes whole-genome association study in four populations: The DiaGen consortium American Journal of Human Genetics. 81: 338-345. PMID 17668382 DOI: 10.1086/520599 |
0.559 |
|
| 2007 |
Dina C, Meyre D, Gallina S, Durand E, Körner A, Jacobson P, Carlsson LM, Kiess W, Vatin V, Lecoeur C, Delplanque J, Vaillant E, Pattou F, Ruiz J, Weill J, et al. Variation in FTO contributes to childhood obesity and severe adult obesity. Nature Genetics. 39: 724-6. PMID 17496892 DOI: 10.1038/Ng2048 |
0.58 |
|
| 2004 |
Meyre D, Lecoeur C, Delplanque J, Francke S, Vatin V, Durand E, Weill J, Dina C, Froguel P. A Genome-Wide Scan for Childhood Obesity-Associated Traits in French Families Shows Significant Linkage on Chromosome 6q22.31-q23.2 Diabetes. 53: 803-811. PMID 14988267 DOI: 10.2337/Diabetes.53.3.803 |
0.476 |
|
| 2003 |
Helbecque N, Abderrahamani A, Meylan L, Riederer B, Mooser V, Miklossy J, Delplanque J, Boutin P, Nicod P, Haefliger JA, Cottel D, Amouyel P, Froguel P, Waeber G, Abderrhamani A. Islet-brain1/C-Jun N-terminal kinase interacting protein-1 (IB1/JIP-1) promoter variant is associated with Alzheimer's disease. Molecular Psychiatry. 8: 413-22, 363. PMID 12740599 DOI: 10.1038/Sj.Mp.4001344 |
0.472 |
|
| 2003 |
Veiga-Da-Cunha M, Delplanque J, Gillain A, Bonthron DT, Boutin P, Van Schaftingen E, Froguel P. Mutations in the glucokinase regulatory protein gene in 2p23 in obese French caucasians Diabetologia. 46: 704-711. PMID 12739015 DOI: 10.1007/S00125-003-1083-Y |
0.562 |
|
| 2002 |
Challis BG, Pritchard LE, Creemers JWM, Delplanque J, Keogh JM, Luan J, Wareham NJ, Yeo GSH, Bhattacharyya S, Froguel P, White A, Sadaf Farooqi I, O'Rahilly S. A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism Human Molecular Genetics. 11: 1997-2004. PMID 12165561 DOI: 10.1093/Hmg/11.17.1997 |
0.422 |
|
| 2002 |
Delplanque J, Vasseur F, Durand E, Abderrahmani A, Dina C, Waeber G, Guy-Grand B, Clement K, Weill J, Boutin P, Froguel P. Mutation screening of the urocortin gene: Identification of new single nucleotide polymorphisms and association studies with obesity in French Caucasians Journal of Clinical Endocrinology and Metabolism. 87: 867-869. PMID 11836334 DOI: 10.1210/Jcem.87.2.8259 |
0.734 |
|
| 2000 |
Delplanque J, Barat-Houari M, Dina C, Gallina P, Clément K, Guy-Grand B, Vasseur F, Boutin P, Froguel P. Linkage and association studies between the proopiomelanocortin (POMC) gene and obesity in caucasian families Diabetologia. 43: 1554-1557. PMID 11151766 DOI: 10.1007/S001250051568 |
0.562 |
|
| 2000 |
Waeber G, Delplanque J, Bonny C, Mooser V, Steinmann M, Widmann C, Maillard A, Miklossy J, Dina C, Hani EH, Vionnet N, Nicod P, Boutin P, Froguel P. The gene MAPK8IP1, encoding islet-brain-1, is a candidate for type 2 diabetes. Nature Genetics. 24: 291-5. PMID 10700186 DOI: 10.1038/73523 |
0.729 |
|
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