By Scientia Professor Matthew Colm Kiernan

Preprints

Willemse SW; Roes KCB; Damme PV; Hardiman O; Ingre C; Povedano M; Wray NR; Gijzen M; de Pagter MS; Demaegd KC; Janse AFC; Vink RC; Sleutjes BTHM; Chiò A; Corcia P; Reviers E; Al-Chalabi A; Kiernan MC; Berg LHVD; Es MAV; Eijk RPAV, 2022, Lithium carbonate in Amyotrophic Lateral Sclerosis patients homozygous for the C-allele at SNP rs12608932 in UNC13A; protocol for a confirmatory, randomized, group-sequential, event-driven, double-blind, placebo-controlled trial., , http://dx.doi.org/10.21203/rs.3.rs-2125381/v1

Haidar M; Viden A; Cuic B; Wang T; Rosier M; Tomas D; Mills SA; Govier-Cole A; Djouma E; Luikinga S; Rytova V; Barton SK; Gonsalvez DG; Palmer LM; McLean C; Kiernan MC; Vucic S; Turner BJ, 2021, Cortical hyperexcitability drives dying forward ALS symptoms and pathology in mice, , http://dx.doi.org/10.1101/2021.08.13.456320

Rheenen WV; van der Spek RAA; Bakker M; Vugt JJFAV; Hop P; Zwamborn RAJ; Klein ND; Westra H-J; Bakker O; Deelen P; Shireby G; Hannon E; Moisse M; Baird D; Restuadi R; Dolzhenko E; Dekker A; Gawor K; Westeneng H-J; Tazelaar GHP; van Eijk K; Kooyman M; Byrne R; Doherty M; Heverin M; Khleifat AA; Iacoangeli A; Shatunov A; Ticozzi N; Cooper-Knock J; Smith B; Gromicho M; Chandran S; Pal S; Morrison K; Shaw P; Hardy J; Orrell R; Sendtner M; Meyer T; Başak N; van der Kooi A; Ratti A; Fogh I; Gellera C; Lauria Pinter G; Corti S; Cereda C; Sproviero D; D’Alfonso S; Sorarù G; Siciliano G; Filosto M; Padovani A; Chiò A; Calvo A; Moglia C; Brunetti M; Canosa A; Grassano M; Beghi E; Pupillo E; Logroscino G; Nefussy B; Osmanovic A; Nordin A; Lerner Y; Zabari M; Gotkine M; Baloh R; Bell S; Vourc’h P; Corcia P; Couratier P; Millecamps S; Meininger V; Salachas F; Pardina JM; Assialioui A; Rojas-García R; Dion P; Ross J; Ludolph A; Weishaupt J; Brenner D; Freischmidt A; Bensimon G; Brice A; Dürr A; Payan CAM; Saker-Delye S; Wood N; Topp S; Rademakers R; Tittmann L; Lieb W; Franke A; Ripke S; Braun A; Kraft J; Whiteman D; Olsen C; Uitterlinden A; Hofman A; Rietschel M; Cichon S; Nöthen M; Amouyel P; Traynor B; Singleton A; Neto MM; Cauchi R; Ophoff R; Wiedau-Pazos M; Lomen-Hoerth C; van Deerlin V; Grosskreutz J; Rödiger A; Gaur N; Jörk A; Barthel T; Theele E; Ilse B; Stubendorff B; Witte O; Steinbach R; Hübner C; Graff C; Brylev L; Fominykh V; Demeshonok V; Ataulina A; Rogelj B; Koritnik B; Zidar J; Ravnik-Glavač M; Glavač D; Stević Z; Drory V; Povedano M; Blair I; Kiernan M; Benyamin B; Henderson R; Furlong S; Mathers S; McCombe P; Needham M; Ngo S; Nicholson G; Pamphlett R; Rowe D; Steyn F; Williams K; Mather K; Sachdev P; Henders A; Wallace L; Carvalho MD; Pinto S; Petri S; Osmanovic A; Weber M; Rouleau G; Silani V; Curtis C; Breen G; Glass J; Brown R; Landers J; Shaw C; Andersen P; Groen EJN; Es MV; Pasterkamp J; Fan D; Garton F; McRae A; Davey Smith G; Gaunt T; Eberle M; Mill J; McLaughlin R; Hardiman O; Kenna K; Wray N; Tsai E; Runz H; Franke L; Al-Chalabi A; Damme PV; van den Berg L; Veldink J; SLALOM Consortium ; PARALS Consortium ; SLAGEN Consortium ; SLAP Consortium , 2021, Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology, , http://dx.doi.org/10.1101/2021.03.12.21253159

Rheenen WV; Spek RVD; Bakker M; Berg LVD; Veldink J; Vugt JV; Hop P; Zwamborn R; de Klein N; Westra H-J; Bakker O; Deelen P; Shireby G; Hannon E; Moisse M; Baird D; Restuadi R; Dolzhenko E; Dekker A; Gawor K; Westeneng H-J; Tazelaar G; Eijk KV; Kooyman M; Byrne R; Doherty M; Heverin M; Khleifat AA; Iacoangeli A; Shatunov A; Ticozzi N; Cooper-Knock J; Smith B; Gromicho M; Chandran S; Pal S; Morrison K; Shaw P; Hardy J; Orrell R; Sendtner M; Meyer T; Basak N; Kooi AVD; Ratti A; Fogh I; Gellera C; Pinter GL; Corti S; Cereda C; Sproviero D; D'Alfonso S; Soraru G; Siciliano G; Filosto M; Padovani A; Chio A; Calvo A; Moglia C; Brunetti M; Canosa A; Grassano M; Beghi E; Pupillo E; Logroscino G; Nefussy B; Osmanovic A; Nordin A; Lerner Y; Zabari M; Gotkine M; Baloh R; Bell S; Vourc'h P; Corcia P; Couratier P; Millecamps S; Meininger V; Salachas F; Pardina JM; Assialioui A; Rojas-García R; Dion P; Ross J; Ludolph A; Weishaupt J; Brenner D; Freischmidt A; Bensimon G; Brice A; Durr A; Payan C; Saker-Delye S; Wood N; Topp S; Rademakers R; Tittmann L; Lieb W; Franke A; Ripke S; Braun A; Kraft J; Whiteman D; Olsen C; Uitterlinden A; Hofman A; Rietschel M; Cichon S; Nöthen M; Amouyel P; Traynor B; Singleton A; Neto MM; Cauchi R; Ophoff R; Wiedau-Pazos M; Lomen-Hoerth C; Deerlin VV; Grosskreutz J; Rödiger A; Jörk A; Barthel T; Theele E; Ilse B; Stubendorff B; Witte O; Steinbach R; Hübner C; Graff C; Brylev L; Fominykh V; Demeshonok V; Ataulina A; Rogelj B; Koritnik B; Zidar J; Ravnik-Glavač M; Glavač D; Stević Z; Drory V; Povedano M; Blair I; Kiernan M; Benyamin B; Henderson R; Furlong S; Mathers S; McCombe P; Needham M; Ngo S; Nicholson G; Pamphlett R; Rowe D; Steyn F; Williams K; Mather K; Sachdev P; Henders A; Wallace L; de Carvalho M; Pinto S; Petri S; Weber M; Rouleau G; Silani V; Curtis C; Breen G; Glass J; Brown R; Landers J; Shaw C; Andersen P; Groen E; Es MV; Pasterkamp J; Fan D; Garton F; McRae A; Smith GD; Gaunt T; Eberle M; Mill J; McLaughlin R; Hardiman O; Kenna K; Wray N; Tsai E; Runz H; Franke L; Al-Chalabi A; Damme PV; Gaur N, 2021, Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology, , http://dx.doi.org/10.21203/rs.3.rs-322430/v1

Hop P; Zwamborn RAJ; Hannon E; Shireby G; Nabais M; Walker E; van Rheenen W; van Vugt JJFA; Dekker A; Westeneng H-J; Tazelaar GHP; van Eijk K; Moisse M; Baird D; Khleifat AA; Iacoangeli A; Ticozzi N; Ratti A; Cooper-Knock J; Morrison K; Shaw P; Basak N; Chiò A; Calvo A; Moglia C; Canosa A; Brunetti M; Grassano M; Gotkine M; Lerner Y; Zabari M; Vourc’h P; Corcia P; Couratier P; Mora Pardina J; Salas T; Dion P; Ross J; Henderson R; Mathers S; McCombe P; Needham M; Nicholson G; Rowe D; Pamphlett R; Mather K; Sachdev P; Furlong S; Garton F; Henders A; Lin T; Ngo S; Steyn F; Wallace L; Williams K; Neto MM; Cauchi R; Blair I; Kiernan M; Drory V; Povedano M; de Carvalho M; Pinto S; Weber M; Rouleau G; Silani V; Landers J; Shaw C; Andersen P; McRae A; van Es M; Pasterkamp J; Wray N; McLaughlin R; Hardiman O; Kenna K; Tsai E; Runz H; Al-Chalabi A; van den Berg L; Damme PV; Mill J; Veldink J; BIOS Consortium ; Brain MEND Consortium , 2021, Genome-wide study of DNA methylation in Amyotrophic Lateral Sclerosis identifies differentially methylated loci and implicates metabolic, inflammatory and cholesterol pathways, , http://dx.doi.org/10.1101/2021.03.12.21253115

Henden L; Twine NA; Szul P; McCann EP; Nicholson GA; Rowe DB; Kiernan MC; Bauer DC; Blair IP; Williams KL, 2019, IBD analysis of Australian amyotrophic lateral sclerosis SOD1-mutation carriers identifies five founder events and links sporadic cases to existing ALS families, , http://dx.doi.org/10.1101/685925

Gold J; Rowe DB; Kiernan MC; Vucic S; Mathers S; van Eijk RP; Nath A; Garcia Montojo M; Norato G; Santamaria UA; Rogers M-L; Malaspina A; Lombardi V; Mehta PR; Westeneng H-J; van den Berg LH; Al-Chalabi A, Safety and Tolerability of Triumeq in Amyotrophic Lateral Sclerosis: The Lighthouse Trial, , http://dx.doi.org/10.2139/ssrn.3347916

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