Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (European Journal of Human Genetics, (2021), 29, 9, (1337-1347), 10.1038/s41431-021-00852-7)

Leslie Matalonga et al
Eur J Hum Genet. 2021-08-16; 29(9): 1466-1469
DOI: 10.1038/s41431-021-00934-6

PubMed

Matalonga L(1), Hernández-Ferrer C(1), Piscia D(1); Solve-RD SNV-indel working
group; Schüle R(2), Synofzik M(2)(3), Töpf A(4), Vissers LELM(5)(6), de Voer
R(5)(7); Solve-RD DITF-GENTURIS; Solve-RD DITF-ITHACA; Solve-RD DITF-euroNMD;
Solve-RD DITF-RND; Tonda R(1), Laurie S(1), Fernandez-Callejo M(1), Picó D(1),
Garcia-Linares C(1), Papakonstantinou A(1), Corvó A(1), Joshi R(1), Diez H(1),
Gut I(1), Hoischen A(5)(7)(8), Graessner H(9)(10), Beltran S(11)(12)(13);
Solve-RD Consortium.

Collaborators: Cohen E, Cuesta I, Danis D, Denommé-Pichon AS, Duffourd Y,
Gilissen C, Johari M, Laurie S, Li S, Matalonga L, Nelson I, Peters S, Paramonov
I, Prasanth S, Robinson P, Sablauskas K, Savarese M, Steyaert W, van der Velde
JK, Vitobello A, Aretz S, Capella G, de Voer RM, Evans G, Pelaez JG,
Holinski-Feder E, Hoogerbrugge N, Laner A, Oliveira C, Rump A, Schröck E, Sommer
AK, Steinke-Lange V, Paske IT, Tischkowitz M, Valle L, Banka S, Benetti E,
Casari G, Ciolfi A, Clayton-Smith J, Dallapiccola B, de Boer E, Denommé-Pichon
AS, Ellwanger K, Faivre L, Graessner H, Haack TB, Hammarsjö A, Havlovicova M,
Hoischen A, Hugon A, Jackson A, Kleefstra T, Lindstrand A, López-Martín E, Macek
M Jr, Morleo M, Nigro V, Nordgren A, Pettersson M, Pinelli M, Pizzi S, Posada M,
Radio FC, Renieri A, Rooryck C, Ryba L, Schwarz M, Tartaglia M, Thauvin C,
Torella A, Trimouille A, Verloes A, Vissers L, Vitobello A, Votypka P, Vyshka K,
Zurek B, Baets J, Beijer D, Bonne G, Cohen E, Cossins J, Evangelista T, Ferlini
A, Hackman P, Hanna MG, Horvath R, Houlden H, Johari M, Lau J, Lochmüller H,
Macken WL, Musacchia F, Nascimento A, Natera-de Benito D, Nigro V, Piluso G,
Pini V, Pitceathly RDS, Polavarapu K, Cruz PMR, Sarkozy A, Savarese M, Selvatici
R, Thompson R, Udd B, Van de Vondel L, Vandrovcova J, Zaharieva I, Baets J,
Balicza P, Chinnery P, Dürr A, Haack T, Hengel H, Houlden H, Kamsteeg EJ,
Kamsteeg C, Lohmann K, Macaya A, Marcé-Grau A, Maver A, Molnar J, Münchau A,
Peterlin B, Riess O, Schöls L, Schüle-Freyer R, Stevanin G, Synofzik M,
Timmerman V, van de Warrenburg B, van Os N, Wayand M, Wilke C, Haack TB,
Graessner H, Zurek B, Ellwanger K, Ossowski S, Demidov G, Sturm M,
Schulze-Hentrich JM, Schüle R, Kessler C, Wayand M, Schöls L, Hengel H, Heutink
P, Brunner H, Scheffer H, Hoogerbrugge N, ‘t Hoen PAC, Steyaert W, Sablauskas K,
Kamsteeg EJ, van de Warrenburg B, Te Paske I, Janssen E, Steehouwer M, Yaldiz B,
Brookes AJ, Veal C, Gibson S, Wadsley M, Mehtarizadeh M, Riaz U, Warren G,
Dizjikan FY, Shorter T, Straub V, Bettolo CM, Specht S, Clayton-Smith J, Banka
S, Alexander E, Jackson A, Faivre L, Thauvin C, Duffourd Y, Tisserant E, Bruel
AL, Peyron C, Pélissier A, Beltran S, Gut IG, Laurie S, Piscia D, Matalonga L,
Papakonstantinou A, Bullich G, Corvo A, Garcia C, Fernandez-Callejo M, Hernández
C, Picó D, Paramonov I, Lochmüller H, Gumus G, Bros-Facer V, Rath A, Hanauer M,
Olry A, Lagorce D, Havrylenko S, Izem K, Rigour F, Durr A, Davoine CS,
Guillot-Noel L, Heinzmann A, Coarelli G, Bonne G, Evangelista T, Allamand V,
Nelson I, Yaou RB, Metay C, Eymard B, Cohen E, Atalaia A, Stojkovic T, Macek M
Jr, Turnovec M, Thomasová D, Kremliková RP, Franková V, Havlovicová M, Kremlik
V, Parkinson H, Keane T, Spalding D, Senf A, Danis D, Robert G, Costa A, Patch
C, Hanna M, Houlden H, Reilly M, Vandrovcova J, Muntoni F, Sarkozy A, Timmerman
V, Baets J, Van de Vondel L, Beijer D, de Jonghe P, Banfi S, Torella A, Ferlini
A, Selvatici R, Rossi R, Neri M, Aretz S, Spier I, Peters S, Oliveira C, Pelaez
JG, Matos AR, José CS, Ferreira M, Gullo I, Fernandes S, Garrido L, Ferreira P,
Carneiro F, Swertz MA, Johansson L, van der Vries G, Neerincx PB, Roelofs-Prins
D, Köhler S, Metcalfe A, Rooryck C, Trimouille A, Castello R, Morleo M,
Varavallo A, De la Paz MP, Sánchez EB, Martín EL, Delgado BM, de la Rosa FJAG,
Radio FC, Tartaglia M, Renieri A, Benetti E, Balicza P, Molnar MJ, Maver A,
Peterlin B, Münchau A, Lohmann K, Herzog R, Pauly M, Macaya A, Marcé-Grau A,
Osorio AN, de Benito DN, Lochmüller H, Thompson R, Polavarapu K, Beeson D,
Cossins J, Cruz PMR, Hackman P, Johari M, Savarese M, Udd B, Horvath R, Capella
G, Valle L, Holinski-Feder E, Laner A, Steinke-Lange V, Schröck E, Rump A.

Author information:
(1)CNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of
Science and Technology, Baldiri Reixac 4, Barcelona, Spain.
(2)Department of Neurodegeneration, Hertie Institute for Clinical Brain Research
(HIH), University of Tübingen, Tübingen, Germany.
(3)German Center for Neurodegenerative Diseases (DZNE), Tübingen, Germany.
(4)John Walton Muscular Dystrophy Research Centre, Translational and Clinical
Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation
Trust, Newcastle upon Tyne, UK.
(5)Department of Human Genetics, Radboud University Medical Center, Nijmegen,
The Netherlands.
(6)Donders Institute for Brain, Cognition and Behaviour, Radboud University
Medical Center, Nijmegen, The Netherlands.
(7)Radboud Institute for Molecular Life Sciences, Nijmegen, The Netherlands.
(8)Department of Internal Medicine and Radboud Center for Infectious Diseases
(RCI), Radboud University Medical Center, Nijmegen, The Netherlands.
(9)Institute of Medical Genetics and Applied Genomics, University of Tübingen,
Tübingen, Germany.
(10)European Reference Network for Rare Neurological Diseases, Tübingen,
Germany.
(11)CNAG-CRG, Centre for Genomic Regulation (CRG), The Barcelona Institute of
Science and Technology, Baldiri Reixac 4, Barcelona, Spain.
.
(12)Universitat Pompeu Fabra (UPF), Barcelona, Spain. .
(13)Departament de Genètica, Microbiologia i Estadística, Facultat de Biologia,
Universitat de Barcelona (UB), Barcelona, Spain. .