Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.
Authors :Leitão E
, Santini A
, Cogne B
, Essid M
, Athanasiadou M
, LaFlamme CW
, Marijon P
, Bernard V
, Chatron N
, Barcia G
, Keren B
, Mignot C
, Charles P
, Besnard T
, de Sainte Agathe JM
, Fuerte EPA
, Sengupta S
, Milh M
, Ramond F
, Allan T
, An I
, Araujo C
, Arpin S
, Austin-Tse C
, Auvin S
, Baer S
, Bahi-Buisson N
, Bak M
, Barth M
, Baulac S
, Weirauch NB
, Begemann M
, Bennett MF
, Bensabath U
, Bézieau S
, Bhouri R
, Biehler M
, Hammer TB
, Bogoin J
, Bonanno E
, Boussion S
, Bramswig NC
, Bris C
, Brosseau-Beauvir A
, Bruel AL
, Buratti J
, Chambon P
, Chemaly N
, Chesneau B
, Colin E
, Colmard M
, Conrad S
, Courtin T
, Dang LT
, de Saint Martin A
, de Vanssay de Blavous Legendre C
, Denommé-Pichon AS
, DiTroia S
, Doco-Fenzy M
, Dubourg C
, Dubucs C
, Ducreux S
, Dufour L
, Duquet R
, Durand B
, Chehadeh SE
, Elbracht M
, Faivre L
, Faoucher M
, Faudet A
, Forlani S
, Fradin M
, Gaignard P
, Ganne B
, Garde A
, Géraud J
, Gill D
, Goldenberg A
, Grabli D
, Grisel C
, Gueden S
, Gueguen P
, Guerrot AM
, Guichet A
, Härting N
, Häusler MG
, Heide S
, Héron B
, Héron D
, Heulin M
, Houdayer C
, Isidor B
, Jacquette A
, Januel L
, Jean-Marçais N
, Jousselin K
, Kaiser FJ
, Kaya S
, King C
, Konyukh M
, Kraft F
, Krause J
, Kirstetter R
, Kuechler A
, Kurth I
, Labalme A
, Laloy JS
, Laugel V
, Bricquir FL
, Lèbre AS
, Lebrun M
, Leguern E
, Levy J
, Lieffering N
, Lyonnet S
, Lüthy K
, Macdonald S
, Mansour-Hendili L
, Maraval J
, Mattausch C
, Messaoud O
, Morel G
, Mortreux J
, Munnich A
, Nabbout R
, Nambot S
, Navarro V
, Neale A
, Nguyen L
, Nizon M
, Nowak F
, O'Leary MC
, Odent S
, Ojeda NM
, Olin V
, Õunap K
, Pais LS
, Paluch R
, Panagiotakaki E
, Patat O
, Perrin-Sabourin L
, Petit F
, Philippe C
, Piton A
, Planes M
, Poirsier C
, Pouzet A
, Prouteau C
, Quéméner-Redon S
, Renaud M
, Richard AC
, Rio M
, Rivier C
, Robin-Renaldo F
, Rollier P
, Rossi M
, Roubertie A
, Rupin M
, Saugier-Veber P
, Saneto R
, Sarrazin E
, Schaefer E
, Schluth-Bolard C
, Schneider A
, Schumann I
, Seplyarskiy V
, Smol T
, Sunyaev S
, Sperelakis-Beedham B
, Stenton SL
, Stock F
, Tharreau M
, Torun D
, Toulouse J
, Thiyagarajah H
, Valence S
, Valleix S
, Villard L
, Ville D
, Villeneuve N
, Vitobello A
, Waernessyckle A
, Weber Y
, Wieczorek D
, Witkowski T
, Yadavilli M
, Yammine T
, Zaafrane-Khachnaoui K
, Zaki MS
, Ziegler A
, Lermine A
, Nicolas G
, Gleeson JG
, Sadleir LG
, Hildebrand MS
, Scheffer IE
, Whiffin N
, O'Donnell-Luria A
, Mefford HC
, Blanc P
, Thevenon J
, Charbonnier C
, Charenton C
, Depienne C
, Lesca G
, Nava C
Published On :2025 Sep 4
Journal Article
LONP1 Variants Are Associated With Clinically Diverse Phenotypes.
Authors :Young RE
, Qiao L
, Hernan R
, Sweetser DA
, Waxler JL
, Scott DA
, Scott TM
, Lalani SR
, Azamian MS
, Rosenfeld JA
, Bostwick B
, Burrage LC
, Undiagnosed Diseases Network
, Rodan LH
, Russell BE
, Dutra-Clarke M
, Kruer M
, Bakhtiarim S
, Darvish H
, Amor DJ
, Rahman S
, Stals K
, Bradley L
, Byrne S
, Tolusso LK
, Wong B
, Benedict L
, Wallis K
, Micke K
, Colson C
, Smol T
, Southwick SV
, Miller KA
, Kush ML
, Chorin O
, Rothschild A
, Wang W
, Shen Y
, Chung WK
Published On :2025 Sep 10
Journal Article
ClinGen recuration of hearing loss-associated genes demonstrates significant changes in gene-disease validity over time.
Authors :Tshering KC
, DiStefano MT
, Oza AM
, Ajuyah P
, Webb R
, Edoh E
, Broeren E
, Ratliff J
, Gitau V
, Paris K
, Aburyyan A
, Alexander J
, Albano V
, Bai D
, Booth KTA
, Buonfiglio PI
, Charfeddine C
, Dalamón V
, Castillo ID
, Moreno-Pelayo MA
, Duzkale H
, Dorshorst B
, Faridi R
, Kenna M
, Lewis MA
, Luo M
, Lu Y
, Mkaouar R
, Matsunaga T
, Nara K
, Pandya A
, Redfield S
, Roux I
, Schimmenti LA
, Schrauwen I
, Shaaban S
, Shen J
, Vona B
, Smith RJ
, Rehm HL
, Azaiez H
, Abou Tayoun AN
, Amr SS
, ClinGen Hearing Loss Clinical Domain Working Group
Published On :2025 Oct
Published Erratum