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TITLE: mRNA therapy corrects defective glutathione metabolism and restores ureagenesis in preclinical argininosuccinic aciduria
AUTHORS: Gurung, Sonam; Timmermand, Oskar Vilhelmsson; Perocheau, Dany; Gil Martinez, Ana Luisa; Minnion, Magdalena; Touramanidou, Loukia; Fang, Sherry; Messina, Martina; Khalil, Youssef; Spiewak, Justyna; Barber, Abigail R.; Edwards, Richard S.; Pinto, Patricia Lipari; Finn, Patrick F.; Cavedon, Alex; Siddiqui, Summar; Rice, Lisa; Martini, Paolo G. V.; Ridout, Deborah; Heywood, Wendy; Hargreaves, Ian; Heales, Simon; Mills, Philippa B.; Waddington, Simon N.; Gissen, Paul; Eaton, Simon; Ryten, Mina; Feelisch, Martin; Frassetto, Andrea; Witney, Timothy H.; Baruteau, Julien; ...More
PUBLISHED: 2024, SOURCE: SCIENCE TRANSLATIONAL MEDICINE, VOLUME: 16, ISSUE: 729
INDEXED IN: Scopus WOS
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TITLE: Gain-of-function mutations in the phosphatidylserine synthase 1 (PTDSS1) gene cause Lenz-Majewski syndrome  Full Text
AUTHORS: Sergio B Sousa; Dagan Jenkins; Estelle Chanudet; Guergana Tasseva; Miho Ishida; Glenn Anderson; James Docker; Mina Ryten; Joaquim Sa; Jorge M Saraiva; Angela Barnicoat; Richard Scott; Alistair Calder; Duangrurdee Wattanasirichaigoon; Krystyna Chrzanowska; Martina Simandlova; Lionel Van Maldergem; Philip Stanier; Philip L Beales; Jean E Vance; Gudrun E Moore; ...More
PUBLISHED: 2014, SOURCE: NATURE GENETICS, VOLUME: 46, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 27
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TITLE: Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
AUTHORS: Anna C Thomas; Hywel Williams; Nuria Seto Salvia; Chiara Bacchelli; Dagan Jenkins; Mary O'Sullivan; Konstantinos Mengrelis; Miho Ishida; Louise Ocaka; Estelle Chanudet; Chela James; Francesco Lescai; Glenn Anderson; Deborah Morrogh; Mina Ryten; Andrew J Duncan; Yun Jin Pai; Jorge M Saraiva; Fabiana Ramos; Bernadette Farren; Dawn Saunders; Bertrand Vernay; Paul Gissen; Anna Straatmaan Iwanowska; Frank Baas; Nicholas W Wood; Joshua Hersheson; Henry Houlden; Jane Hurst; Richard Scott; Maria Bitner Glindzicz; Gudrun E Moore; Sergio B Sousa; Philip Stanier; ...More
PUBLISHED: 2014, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 95, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 25
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TITLE: Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A  Full Text
AUTHORS: Dalia Kasperaviciute; Claudia B Catarino; Mar Matarin; Costin Leu; Jan Novy; Anna Tostevin; Barbara Leal; Ellen V S Hessel; Kerstin Hallmann; Michael S Hildebrand; Hans Henrik M Dahl; Mina Ryten; Daniah Trabzuni; Adaikalavan Ramasamy; Saud Alhusaini; Colin P Doherty; Thomas Dorn; Joerg Hansen; Guenter Kraemer; Bernhard J Steinhoff; Dominik Zumsteg; Susan Duncan; Reetta K Kaelviaeinen; Kai J Eriksson; Anne Mari Kantanen; Massimo Pandolfo; Ursula Gruber Sedlmayr; Kurt Schlachter; Eva M Reinthaler; Elisabeth Stogmann; Fritz Zimprich; Emilie Theatre; Colin Smith; Terence J O'Brien; Meng M Tan; Slave Petrovski; Angela Robbiano; Roberta Paravidino; Federico Zara; Pasquale Striano; Michael R Sperling; Russell J Buono; Hakon Hakonarson; Joao Chaves; Paulo P Costa ; Berta M Silva ; Antonio M da Silva ; Pierre N E de Graan; Bobby P C Koeleman; Albert Becker; Susanne Schoch; Marec von Lehe; Philipp S Reif; Felix Rosenow; Felicitas Becker; Yvonne Weber; Holger Lerche; Karl Roessler; Michael Buchfelder; Hajo M Hamer; Katja Kobow; Roland Coras; Ingmar Blumcke; Ingrid E Scheffer; Samuel F Berkovic; Michael E Weale; Norman Delanty; Chantal Depondt; Gianpiero L Cavalleri; Wolfram S Kunz; Sanjay M Sisodiya; ...More
PUBLISHED: 2013, SOURCE: BRAIN, VOLUME: 136, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef
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TITLE: TREM2 Variants in Alzheimer's Disease
AUTHORS: Rita Guerreiro; Aleksandra Wojtas; Jose Bras; Minerva Carrasquillo; Ekaterina Rogaeva; Elisa Majounie; Carlos Cruchaga; Celeste Sassi; John S K Kauwe; Michelle K Lupton; Mina Ryten; Kristelle Brown; James Lowe; Perry G Ridge; Monia B Hammer; Yosuke Wakutani; Petroula Proitsi; Stephen Newhouse; Ebba Lohmann; Nihan Erginel Unaltuna; Christopher Medway; Hasmet Hanagasi; Claire Troakes; Hakan Gurvit; Basar Bilgic; Safa Al Sarraj; Bruno Benitez; Breanna Cooper; David Carrell; Murat Emre; Fanggeng G Zou; Li Ma; Melissa E Murray; Dennis W Dickson; Steven Younkin; Lilinaz Hazrati; Ronald C Petersen; Christopher D Corcoran; Yefei F Cai; Catarina Oliveira; Maria Helena Ribeiro; Isabel Santana; JoAnn T Tschanz; Raphael R Gibbs; Maria C Norton; Iwona Kloszewska; Patrizia Mecocci; Hilkka Soininen; Magda Tsolaki; Bruno Vellas; Ronald G Munger; David M A Mann; Stuart Pickering Brown; Simon Lovestone; Jonathan Beck; Simon Mead; John Collinge; Linda Parsons; Jennifer Pocock; John C Morris; Tamas Revesz; Tammaryn Lashley; Nick C Fox; Martin N Rossor; Benjamin Grenier Boley; Celine Bellenguez; Valentina Moskvina; Rebecca Sims; Denise Harold; Julie Williams; Jean Charles Lambert; Philippe Amouyel; Neill Graff Radford; Alison Goate; Rosa Rademakers; Kevin Morgan; John Powell; Peter St George Hyslop; Andrew Singleton; John Hardy; ...More
PUBLISHED: 2013, SOURCE: NEW ENGLAND JOURNAL OF MEDICINE, VOLUME: 368, ISSUE: 2
INDEXED IN: WOS CrossRef: 911