2016

1          M. Ailem, F. Role, M. Nadif, and F. Demenais, ‘Unsupervised Text Mining for Assessing and Augmenting Gwas Results’, J Biomed Inform, 60 (2016), 252-9.

2          S. Benhamou, J. Bonastre, K. Groussard, F. Radvanyi, Y. Allory, and T. Lebret, ‘A Prospective Multicenter Study on Bladder Cancer: The Coblance Cohort’, BMC Cancer, 16 (2016), 837.

3          C. Bertolotto, F. Lesueur, S. Giuliano, T. Strub, M. de Lichy, K. Bille, P. Dessen, B. d’Hayer, H. Mohamdi, A. Remenieras, E. Maubec, A. de la Fouchardiere, V. Molinie, P. Vabres, S. Dalle, N. Poulalhon, T. Martin-Denavit, L. Thomas, P. Andry-Benzaquen, N. Dupin, F. Boitier, A. Rossi, J. L. Perrot, B. Labeille, C. Robert, B. Escudier, O. Caron, L. Brugieres, S. Saule, B. Gardie, S. Gad, S. Richard, J. Couturier, B. T. Teh, P. Ghiorzo, L. Pastorino, S. Puig, C. Badenas, H. Olsson, C. Ingvar, E. Rouleau, R. Lidereau, P. Bahadoran, P. Vielh, E. Corda, H. Blanche, D. Zelenika, P. Galan, V. Chaudru, G. M. Lenoir, M. Lathrop, I. Davidson, M. F. Avril, F. Demenais, R. Ballotti, and B. Bressac-de Paillerets, ‘Corrigendum: A Sumoylation-Defective Mitf Germline Mutation Predisposes to Melanoma and Renal Carcinoma’, Nature, 531 (2016), 126.

4          S. H. Choi, D. Ruggiero, R. Sorice, C. Song, T. Nutile, A. Vernon Smith, M. P. Concas, M. Traglia, C. Barbieri, N. C. Ndiaye, M. G. Stathopoulou, V. Lagou, G. B. Maestrale, C. Sala, S. Debette, P. Kovacs, L. Lind, J. Lamont, P. Fitzgerald, A. Tonjes, V. Gudnason, D. Toniolo, M. Pirastu, C. Bellenguez, R. S. Vasan, E. Ingelsson, A. L. Leutenegger, A. D. Johnson, A. L. DeStefano, S. Visvikis-Siest, S. Seshadri, and M. Ciullo, ‘Six Novel Loci Associated with Circulating Vegf Levels Identified by a Meta-Analysis of Genome-Wide Association Studies’, PLoS Genet, 12 (2016), e1005874.

5          M. H. Dizier, R. Nadif, P. Margaritte-Jeannin, S. J. Barton, C. Sarnowski, V. Gagne-Ouellet, M. Brossard, N. Lavielle, J. Just, M. Lathrop, J. W. Holloway, C. Laprise, E. Bouzigon, and F. Demenais, ‘Interaction between the Dnah9 Gene and Early Smoke Exposure in Bronchial Hyperresponsiveness’, Eur Respir J, 47 (2016), 1072-81.

6          S. Fang, A. Vaysse, M. Brossard, Y. Wang, D. Deng, Q. Liu, P. Zhang, K. Xu, M. Li, R. Feng, H. Liu, Y. Dang, W. Chen, V. Prieto, J. E. Gershenwald, M. I. Ross, B. Matejka, J. Malke, L. E. Haydu, J. D. Reveille, D. Sui, R. L. Bassett, Jr., N. Koshkina, M. F. Avril, M. Lu, Q. Wei, F. Demenais, C. I. Amos, and J. E. Lee, ‘Melanoma Expression Genes Identified through Genome-Wide Association Study of Breslow Tumor Thickness’, J Invest Dermatol, 137 (2017), 253-57.

7          J. D. Figueroa, C. D. Middlebrooks, A. R. Banday, Y. Ye, M. Garcia-Closas, N. Chatterjee, S. Koutros, L. A. Kiemeney, T. Rafnar, T. Bishop, H. Furberg, G. Matullo, K. Golka, M. Gago-Dominguez, J. A. Taylor, T. Fletcher, A. Siddiq, V. K. Cortessis, C. Kooperberg, O. Cussenot, S. Benhamou, J. Prescott, S. Porru, C. P. Dinney, N. Malats, D. Baris, M. P. Purdue, E. J. Jacobs, D. Albanes, Z. Wang, C. C. Chung, S. H. Vermeulen, K. K. Aben, T. E. Galesloot, G. Thorleifsson, P. Sulem, K. Stefansson, A. E. Kiltie, M. Harland, M. Teo, K. Offit, J. Vijai, D. Bajorin, R. Kopp, G. Fiorito, S. Guarrera, C. Sacerdote, S. Selinski, J. G. Hengstler, H. Gerullis, D. Ovsiannikov, M. Blaszkewicz, J. E. Castelao, M. Calaza, M. E. Martinez, P. Cordeiro, Z. Xu, V. Panduri, R. Kumar, E. Gurzau, K. Koppova, H. B. Bueno-De-Mesquita, B. Ljungberg, F. Clavel-Chapelon, E. Weiderpass, V. Krogh, M. Dorronsoro, R. C. Travis, A. Tjonneland, P. Brennan, J. Chang-Claude, E. Riboli, D. Conti, M. C. Stern, M. C. Pike, D. Van Den Berg, J. M. Yuan, C. Hohensee, R. P. Jeppson, G. Cancel-Tassin, M. Roupret, E. Comperat, C. Turman, I. De Vivo, E. Giovannucci, D. J. Hunter, P. Kraft, S. Lindstrom, A. Carta, S. Pavanello, C. Arici, G. Mastrangelo, A. M. Kamat, L. Zhang, Y. Gong, X. Pu, A. Hutchinson, L. Burdett, W. A. Wheeler, M. R. Karagas, A. Johnson, A. Schned, G. M. Monawar Hosain, M. Schwenn, M. Kogevinas, A. Tardon, C. Serra, A. Carrato, R. Garcia-Closas, J. Lloreta, G. Andriole, Jr., R. Grubb, 3rd, A. Black, W. R. Diver, S. M. Gapstur, S. Weinstein, J. Virtamo, C. A. Haiman, M. T. Landi, N. E. Caporaso, J. F. Fraumeni, Jr., P. Vineis, X. Wu, S. J. Chanock, D. T. Silverman, L. Prokunina-Olsson, and N. Rothman, ‘Identification of a Novel Susceptibility Locus at 13q34 and Refinement of the 20p12.2 Region as a Multi-Signal Locus Associated with Bladder Cancer Risk in Individuals of European Ancestry’, Hum Mol Genet, 25 (2016), 1203-14.

8          S. Gazal, E. Genin, and A. L. Leutenegger, ‘Relationship Inference from the Genetic Data on Parents or Offspring: A Comparative Study’, Theor Popul Biol, 107 (2016), 31-8.

9          S. Gazal, S. Gosset, E. Verdura, F. Bergametti, S. Guey, M. C. Babron, and E. Tournier-Lasserve, ‘Can Whole-Exome Sequencing Data Be Used for Linkage Analysis?’, Eur J Hum Genet, 24 (2016), 581-6.

10        M. E. Goossens, F. Isa, M. Brinkman, D. Mak, R. Reulen, A. Wesselius, S. Benhamou, C. Bosetti, B. Bueno-de-Mesquita, A. Carta, M. F. Allam, K. Golka, E. J. Grant, X. Jiang, K. C. Johnson, M. R. Karagas, E. Kellen, C. La Vecchia, C. M. Lu, J. Marshall, K. Moysich, H. Pohlabeln, S. Porru, G. Steineck, M. C. Stern, L. Tang, J. A. Taylor, P. van den Brandt, P. J. Villeneuve, K. Wakai, E. Weiderpass, E. White, A. Wolk, Z. F. Zhang, F. Buntinx, and M. P. Zeegers, ‘International Pooled Study on Diet and Bladder Cancer: The Bladder Cancer, Epidemiology and Nutritional Determinants (Blend) Study: Design and Baseline Characteristics’, Arch Public Health, 74 (2016), 30.

11        S. Lesage, V. Drouet, E. Majounie, V. Deramecourt, M. Jacoupy, A. Nicolas, F. Cormier-Dequaire, S. M. Hassoun, C. Pujol, S. Ciura, Z. Erpapazoglou, T. Usenko, C. A. Maurage, M. Sahbatou, S. Liebau, J. Ding, B. Bilgic, M. Emre, N. Erginel-Unaltuna, G. Guven, F. Tison, C. Tranchant, M. Vidailhet, J. C. Corvol, P. Krack, A. L. Leutenegger, M. A. Nalls, D. G. Hernandez, P. Heutink, J. R. Gibbs, J. Hardy, N. W. Wood, T. Gasser, A. Durr, J. F. Deleuze, M. Tazir, A. Destee, E. Lohmann, E. Kabashi, A. Singleton, O. Corti, and A. Brice, ‘Loss of Vps13c Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases Pink1/Parkin-Dependent Mitophagy’, Am J Hum Genet, 98 (2016), 500-13.

12        S. J. Lubbe, V. Escott-Price, A. Brice, T. Gasser, A. M. Pittman, J. Bras, J. Hardy, P. Heutink, N. M. Wood, A. B. Singleton, D. G. Grosset, C. B. Carroll, M. H. Law, F. Demenais, M. M. Iles, D. T. Bishop, J. Newton-Bishop, N. M. Williams, and H. R. Morris, ‘Rare Variants Analysis of Cutaneous Malignant Melanoma Genes in Parkinson’s Disease’, Neurobiol Aging, 48 (2016), 222 e1-22 e7.

13        A. M. Madore, V. T. Vaillancourt, E. Bouzigon, C. Sarnowski, F. Monier, M. H. Dizier, F. Demenais, and C. Laprise, ‘Genes Involved in Interleukin-1 Receptor Type Ii Activities Are Associated with Asthmatic Phenotypes’, Allergy Asthma Immunol Res, 8 (2016), 466-70.

14        B. Marin, F. Boumediene, G. Logroscino, P. Couratier, M. C. Babron, A. L. Leutenegger, M. Copetti, P. M. Preux, and E. Beghi, ‘Variation in Worldwide Incidence of Amyotrophic Lateral Sclerosis: A Meta-Analysis’, Int J Epidemiol (2016).

15        B. Marin, G. Logroscino, F. Boumediene, A. Labrunie, P. Couratier, M. C. Babron, A. L. Leutenegger, P. M. Preux, and E. Beghi, ‘Clinical and Demographic Factors and Outcome of Amyotrophic Lateral Sclerosis in Relation to Population Ancestral Origin’, Eur J Epidemiol, 31 (2016), 229-45.

16        C. Minelli, C. H. Dean, M. Hind, A. C. Alves, A. F. Amaral, V. Siroux, V. Huikari, M. Soler Artigas, D. M. Evans, D. W. Loth, Y. Bosse, D. S. Postma, D. Sin, J. Thompson, F. Demenais, J. Henderson, E. Bouzigon, D. Jarvis, M. R. Jarvelin, and P. Burney, ‘Association of Forced Vital Capacity with the Developmental Gene Ncor2’, PLoS One, 11 (2016), e0147388.

17        M. A. Nieuwenhuis, J. M. Vonk, B. E. Himes, C. Sarnowski, C. Minelli, D. Jarvis, E. Bouzigon, D. C. Nickle, M. Laviolette, D. Sin, S. T. Weiss, M. van den Berge, G. H. Koppelman, and D. S. Postma, ‘Pttg1ip and Maml3, Novel Genomewide Association Study Genes for Severity of Hyperresponsiveness in Adult Asthma’, Allergy (2016).

18        M. Rava, I. Ahmed, M. Kogevinas, N. Le Moual, E. Bouzigon, I. Curjuric, M. H. Dizier, O. Dumas, J. R. Gonzalez, M. Imboden, A. J. Mehta, P. Tubert-Bitter, J. P. Zock, D. Jarvis, N. M. Probst-Hensch, F. Demenais, and R. Nadif, ‘Genes Interacting with Occupational Exposures to Low Molecular Weight Agents and Irritants on Adult-Onset Asthma in Three European Studies’, Environ Health Perspect (2016).

19        C. Sarnowski, C. Laprise, G. Malerba, M. F. Moffatt, M. H. Dizier, A. Morin, Q. B. Vincent, K. Rohde, J. Esparza-Gordillo, P. Margaritte-Jeannin, L. Liang, Y. A. Lee, J. Bousquet, V. Siroux, P. F. Pignatti, W. O. Cookson, M. Lathrop, T. Pastinen, F. Demenais, and E. Bouzigon, ‘DNA Methylation within Melatonin Receptor 1a (Mtnr1a) Mediates Paternally Transmitted Genetic Variant Effect on Asthma Plus Rhinitis’, J Allergy Clin Immunol, 138 (2016), 748-53.

20        C. Sarnowski, P. E. Sugier, R. Granell, D. Jarvis, M. H. Dizier, M. Ege, M. Imboden, C. Laprise, E. K. Khusnutdinova, M. B. Freidin, W. O. Cookson, M. Moffatt, M. Lathrop, V. Siroux, L. M. Ogorodova, A. S. Karunas, A. James, N. M. Probst-Hensch, E. von Mutius, I. Pin, M. Kogevinas, A. J. Henderson, F. Demenais, and E. Bouzigon, ‘Identification of a New Locus at 16q12 Associated with Time to Asthma Onset’, J Allergy Clin Immunol, 138 (2016), 1071-80.

21        N. J. Taylor, E. A. Handorf, N. Mitra, M. F. Avril, E. Azizi, W. Bergman, G. Bianchi-Scarra, D. T. Bishop, B. Bressac-de Paillerets, D. Calista, L. A. Cannon-Albright, F. Cuellar, A. E. Cust, F. Demenais, D. E. Elder, E. Friedman, A. M. Gerdes, P. Ghiorzo, A. M. Goldstein, T. C. Grazziotin, J. Hansson, N. K. Hayward, M. Hocevar, V. Hoiom, E. A. Holland, C. Ingvar, M. T. Landi, G. Landman, A. Larre-Borges, S. A. Leachman, G. J. Mann, E. Nagore, H. Olsson, J. Palmer, B. Peric, D. Pjanova, S. Puig, H. Schmid, N. van der Stoep, M. A. Tucker, K. A. Wadt, L. Whitaker, X. R. Yang, J. A. Newton Bishop, N. A. Gruis, and P. A. Kanetsky, ‘Phenotypic and Histopathological Tumor Characteristics According to Cdkn2a Mutation Status among Affected Members of Melanoma Families’, J Invest Dermatol, 136 (2016), 1066-9.

22        A. Vaysse, S. Fang, M. Brossard, Q. Wei, W. V. Chen, H. Mohamdi, L. Vincent-Fetita, P. Margaritte-Jeannin, N. Lavielle, E. Maubec, M. Lathrop, M. F. Avril, C. I. Amos, J. E. Lee, and F. Demenais, ‘A Comprehensive Genome-Wide Analysis of Melanoma Breslow Thickness Identifies Interaction between Cdc42 and Scin Genetic Variants’, Int J Cancer, 139 (2016), 2012-20.