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The Journal of Clinical Endocrinology & Metabolism, ISSN 0021-972X, 03/2019
There is an ongoing debate on whether and how fructose is involved in the pathogenesis of nonalcoholic fatty liver disease (NAFLD). A recent experimental study... 
Journal Article
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 17641 - 9
The range of applications performed on dried blood spots (DBS) widely broadened during the past decades to now include next-generation sequencing (NGS).... 
WHOLE-GENOME | ERA | MULTIDISCIPLINARY SCIENCES | MASS-SPECTROMETRY | CHILDREN | Databases | Mutation | Metabolism | Medical screening | Bioinformatics | Blood | Deoxyribonucleic acid--DNA | Metabolic disorders
Journal Article
Annals of Endocrinology (Annales D'Endocrinologie, English Edition), ISSN 0003-4266, 2017, Volume 78, Issue 3, pp. 188 - 190
Journal Article
NeuroImage, 09/2019, pp. 116155 - 116155
Journal Article
by Heard, Jean-Michel and Bellettato, Cinzia and Van Lingen, Corine and Scarpa, Maurizio and Debray, François-Guillaume and Nassogne, Marie-Cécile and Van Coster, Rudy and De Meirleir, Linda and Eyskens, François and Morava, Eva and Baric, Ivo and Kozich, Viktor and Lund, Allan Meldgaard and Germain, Dominique and Belmatoug, Nadia and Guffon, Nathalie and Labrune, Philippe and Gouya, Laurent and De Lonlay, Pascale and Schiff, Manuel and Dobbelaere, Dries and Chabrol, Brigitte and Das, Anihb Martin and Spiekerkoetter, Ute and Rutsch, Frank and Ploeckinger, Ursula and Mohnike, Klaus and Hahn, Andreas and Kölker, Stefan and Ullrich, Kurt and Balogh, István and Bembi, Bruno and Donati, Maria Alice and Gasperini, Serena and Parenti, Giancarlo and Salviati, Alessandro and Vici, Carlo-Dionisi and Di Rocco, Maja and Cefalo, Graziella and Burlina, Alberto and Ceccarini, Giovanni and Federico, Antonio and Van Der Ploeg, Ans and Rubio-Gozalbo, Maria-Estela and Van Spronsen, Francian and Visser, Gepke and Bosch, Annet and Tangeraas, Trine and Sanderberg, Sverre and Kieć-Wilk, Beata and Gaspar, Ana-Maria Simões Mendes and Martins, Esmeralda and Silva, Esmeralda-Maria Ferreira Rodrigues and De Abreu Freire Diogo Matos, Luísa-Maria and Azevedo, Olga and Tansek, Mojca-Zerjav and Couce-Pico, Maria-Luz and Cazorla, Angeles Garcia and Azuara, Luis Aldámiz-Echevarría and Del Toro-Riera, Mireia and Lajic, Svetlana and Darin, Niklas and Deegan, Patrick and Vijaym, Suresh and Chronopoulou, Efstathia and Jones, Simon and Chakrapani, Anupanm and Hiwot, Tarekegn and MetabERN collaboration group and the MetabERN collaboration group
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 05/2019, Volume 14, Issue 1, pp. 119 - 119
Journal Article
by Martin-Brevet, Sandra and Rodríguez-Herreros, Borja and Nielsen, Jared A and Moreau, Clara and Modenato, Claudia and Maillard, Anne M and Pain, Aurélie and Richetin, Sonia and Jønch, Aia E and Qureshi, Abid Y and Zürcher, Nicole R and Conus, Philippe and Addor, Marie-Claude and Andrieux, Joris and Arveiler, Benoît and Baujat, Geneviève and Sloan-Béna, Frédérique and Belfiore, Marco and Bonneau, Dominique and Bouquillon, Sonia and Boute, Odile and Brusco, Alfredo and Busa, Tiffany and Caberg, Jean-Hubert and Campion, Dominique and Colombert, Vanessa and Cordier, Marie-Pierre and David, Albert and Debray, François-Guillaume and Delrue, Marie-Ange and Doco-Fenzy, Martine and Dunkhase-Heinl, Ulrike and Edery, Patrick and Fagerberg, Christina and Faivre, Laurence and Forzano, Francesca and Genevieve, David and Gérard, Marion and Giachino, Daniela and Guichet, Agnès and Guillin, Olivier and Héron, Delphine and Isidor, Bertrand and Jacquette, Aurélia and Jaillard, Sylvie and Journel, Hubert and Keren, Boris and Lacombe, Didier and Lebon, Sébastien and Le Caignec, Cédric and Lemaître, Marie-Pierre and Lespinasse, James and Mathieu-Dramart, Michèle and Mercier, Sandra and Mignot, Cyril and Missirian, Chantal and Petit, Florence and Pilekær Sørensen, Kristina and Pinson, Lucile and Plessis, Ghislaine and Prieur, Fabienne and Rooryck-Thambo, Caroline and Rossi, Massimiliano and Sanlaville, Damien and Schlott Kristiansen, Britta and Schluth-Bolard, Caroline and Till, Marianne and Van Haelst, Mieke and Van Maldergem, Lionel and Alupay, Hanalore and Aaronson, Benjamin and Ackerman, Sean and Ankenman, Katy and Anwar, Ayesha and Atwell, Constance and Bowe, Alexandra and Beaudet, Arthur L and Benedetti, Marta and Berg, Jessica and Berman, Jeffrey and Berry, Leandra N and Bibb, Audrey L and Blaskey, Lisa and Brennan, Jonathan and Brewton, Christie M and Buckner, Randy and Buckner, Randy L and Bukshpun, Polina and Burko, Jordan and Cali, Phil and Cerban, Bettina and Chang, Yishin and Cheong, Maxwell and Chow, Vivian and Chu, Zili and Chudnovskaya, Darina and Cornew, Lauren and Dale, Corby and Dell, John and Dempsey, Allison G and ... and 16p11 2 European Consorti and Simons Variation Individuals and Simons Variation in Individuals Project (VIP) Consortium and 16p11.2 European Consortium and Gillberg Neuropsychiatry Centre and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Gillbergcentrum and Sahlgrenska Academy
Biological Psychiatry, ISSN 0006-3223, 08/2018, Volume 84, Issue 4, pp. 253 - 264
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 01/2018, Volume 26, Issue 1, pp. 64 - 74
Journal Article
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