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The burden of early onset psychosis: Diagnostic complexity, high comorbidity, and poor functioning in patients and their relatives.

Authors :Mollon J , Lanzagorta N , Mathias SR , Rodrigue A , Knowles EEM , Deaso E , Cadavid L , Saavedra JU , Brownstein C , D'Angelo E , Gonzalez-Heydrich J , Ramírez PZ , Sarmiento E , Bustamante C , Walsh CA , Almasy L , Nicolini H , Glahn DC
Published On :2025 Sep 26
Journal Article


Courtship vocalizations in male ducks: spectral composition and resonance of the syringeal bulla.

Authors :Mishkind D , Kaneelil PR , Lester M , Mahadevan L , Tabin CJ , Goller F
Published On :2025 Sep 26
Journal Article


Homocystinuria due to Cystathionine Beta-Synthase Deficiency.

Authors :Adam MP , Feldman J , Mirzaa GM , Pagon RA , Wallace SE , Amemiya A , Sacharow SJ , Levy HL
Published On :1993
Review


Does DeepSeek curb the surge of energy consumption in data centers?

Authors :Wang Y , Han Y , Han K , Shen J
Published On :2025 Sep 8
Journal Article Review


Transcriptome-wide outlier approach identifies individuals with minor spliceopathies.

Authors :Arriaga TM , Mendez R , Ungar RA , Bonner DE , Matalon DR , Lemire G , Goddard PC , Padhi EM , Miller AM , Nguyen JV , Ma J , Smith KS , Scott SA , Liao L , Ng Z , Marwaha S , Bademci G , Bivona SA , Tekin M , Undiagnosed Diseases Network , Genomics Research to Elucidate the Genetics of Rare Diseases consortium , Bernstein JA , Montgomery SB , O'Donnell-Luria A , Wheeler MT , Ganesh VS
Published On :2025 Oct 2
Journal Article



Patient-Reported Outcomes From Males Regarding Germline Testing for Prostate Cancer: Results From the PROGRESS Registry.

Authors :Loeb S , Keith SW , Gross L , Hartman RL , Beer TM , Brierley KL , Cheng HH , Couvillon A , Dicker AP , Friedman S , Gomella LG , Karsh L , Kelly WK , Lallas CD , Leader AE , Mann MJ , Mark JR , Mille P , Paller CJ , Rana HQ , Sokolova AO , Trabulsi EJ , Whang YE , Giri VN
Published On :2025 Sep
Journal Article


Pan-UK Biobank genome-wide association analyses enhance discovery and resolution of ancestry-enriched effects.

Authors :Karczewski KJ , Gupta R , Kanai M , Lu W , Tsuo K , Wang Y , Walters RK , Turley P , Callier S , Shah NN , Baya N , Palmer DS , Goldstein JI , Sarma G , Solomonson M , Cheng N , Bryant S , Churchhouse C , Cusick CM , Poterba T , Compitello J , King D , Zhou W , Seed C , Finucane HK , Daly MJ , Neale BM , Atkinson EG , Martin AR
Published On :2025 Oct
Journal Article Meta-Analysis



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


Stability of Root Coverage Outcomes After Soft-Tissue Augmentation With a Collagen Matrix With or Without rhPDGF-BB: A 3-Year Triple-Blinded, Randomised, Placebo-Controlled Trial.

Authors :Tavelli L , Barootchi S , Rodriguez MV , Mancini L , Sabri H , Nguyen T , Majzoub J , Travan S , Giannobile WV
Published On :2025 Sep 11
Journal Article


Autoimmune disease risk gene ANKRD55 promotes TH17 effector function through metabolic modulation.

Authors :Xu J , Kong L , Creasey EA , Rath S , Deng L , Avila-Pacheco J , Li C , Oliver BA , Dao TT , Shih AR , Daly MJ , Shalek AK , Clish CB , Graham DB , Deguine J , Xavier RJ
Published On :2025 Nov 3
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


Simultaneous in vivo detection of spectrally resolved glutamate, glutamine, and glutathione at 3 T with NAA-aspartyl editing and echo-time optimization.

Authors :An L , Hong S , Turon T , Pavletic AJ , Johnson CS , Shen J
Published On :2025 Sep 8
Journal Article