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    • Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland 

      Järvelä, Irma; Määttä, Tuomo; Acharya, Anushree; Leppälä, Juha; Jhangiani, Shalini N.; Arvio, Maria; Siren, Auli; Kankuri-Tammilehto, Minna; Kokkonen, Hannaleena; Palomäki, Maarit; Varilo, Teppo; Fang, Mary; Hadley, Trevor D.; Jolly, Angad; Linnankivi, Tarja; Paetau, Ritva; Saarela, Anni; Kälviäinen, Reetta; Olme, Jan; Nouel-Saied, Liz M.; Cornejo-Sanchez, Diana M.; Llaci, Lorida; Lupski, James R.; Posey, Jennifer E.; Leal, Suzanne M.; Schrauwen, Isabelle (12.03.2021)
      article
      The genetics of autosomal recessive intellectual disability (ARID) has mainly been studied in consanguineous families, however, founder populations may also be of interest to study intellectual disability (ID) and the ...