Blauhut, Veit ; Stoelzle, Michael ; Ahopelto, Lauri...
Blauhut , V , Stoelzle , M , Ahopelto , L , Brunner , M I , Wendt , D , Teutschbein , C , Akstinas , V , Bakke , S , Barker , L , Bartošová , L , Briede , A , Cammalleri , C , Cindrić Kalin , K , De Stefano , L , Fendekova , M , Finger , D , Huysmans , M , Ivanov , M , Jaagus , J , Jakubínský , J , Krakovska , S , Laaha , G , Lakatos , M , Manevski , K , Neumann Andersen , M , Nikolova , N , Osuch , M , van Oel , P R , Radeva , K , Romanowicz , R , Toth , E , Trnka , M , Urošev , M , Urquijo Reguera , J , Sauquet , E , Stevkov , A , Tallaksen , L M , Trofimova , I , Van Loon , A , van Vliet , M T H , Vidal , J-P , Wanders , N , Werner , M , Willems , P & Živković , N 2022 , ' Lessons from the 2018–2019 European droughts: a collective need for unifying drought risk management ' , Natural Hazards and Earth System Sciences , vol. 22 , no. 6 , 22 , pp. 2201–2217 . https://doi.org/10.5194/nhess-22-2201-2022.  , 2022

Faundes, Víctor ; Goh, Stephanie ; Akilapa, Rhoda...
Faundes , V , Goh , S , Akilapa , R , Bezuidenhout , H , Bjornsson , H T , Brady , A F , Brischoux-Boucher , E , Brunner , H , Bulk , S , Canham , N , Cody , D , Dentici , M L , Digilio , M C , Elmslie , F , Fry , A E , Gill , H , Hurst , J , Johnson , D , Julia , S , Lachlan , K , Lebel , R R , Byler , M , Gershon , E , Lemire , E , Gnazzo , M , Lepri , F R , Marchese , A , McEntagart , M , McGaughran , J , Mizuno , S , Okamoto , N , Rieubland , C , Sasaki , E , Scalais , E , Scurr , I , Suri , M , van der Burgt , I , Matsumoto , N , Miyake , N , Benoit , V , Lederer , D & Banka , S 2021 , ' Clinical delineation, sex differences, and genotype-phenotype correlation in pathogenic KDM6A variants causing X-linked Kabuki syndrome type 2 ' , Genetics in Medicine . https://doi.org/10.1038/s41436-021-01119-8.  , 2021

den Hoed, J ; de Boer, E ; Voisin, N...
den Hoed , J , de Boer , E , Voisin , N , Dingemans , A J M , Guex , N , Wiel , L , Nellaker , C , Amudhavalli , S M , Banka , S , Bena , F S , Ben-Zeev , B , Bonagura , V R , Bruel , A L , Brunet , T , Brunner , H G , Chew , H B , Chrast , J , Cimbalistiene , L , Coon , H , Delot , E C , Demurger , F , Denomme-Pichon , A S , Depienne , C , Donnai , D , Dyment , D A , Elpeleg , O , Faivre , L , Gilissen , C , Granger , L , Haber , B , Hachiya , Y , Abedi , Y H , Hanebeck , J , Hehir-Kwa , J Y , Horist , B , Itai , T , Jackson , A , Jewell , R , Jones , K L , Joss , S , Kashii , H , Kato , M , Kattentidt-Mouravieva , A A , Kok , F , Kotzaeridou , U , Krishnamurthy , V , Kucinskas , V , Kuechler , A , Lavillaureix , A , Liu , P F , DDD Study & Fisher , S E 2021 , ' Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction ' , American Journal of Human Genetics , vol. 108 , no. 2 , pp. 346-356 . https:/....  , 2021