Elsayed, Fadwa A
35  Ergebnisse:
Personensuche X
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10

Monoallelic NTHL1 Loss-of-Function Variants and Risk of Pol..:

Elsayed, Fadwa A ; Grolleman, Judith E ; Ragunathan, Abiramy...
https://research.rug.nl/en/publications/1c4a43c0-910e-4880-bd55-c0248deb21e5.  , 2020
 
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Mutational Signature Analysis Reveals NTHL1 Deficiency to C..:

Grolleman, Judith E ; de Voer, Richarda M ; Elsayed, Fadwa A...
Grolleman , J E , de Voer , R M , Elsayed , F A , Nielsen , M , Weren , R D A , Palles , C , Ligtenberg , M J L , Vos , J R , ten Broeke , S W , de Miranda , N F C C , Kuiper , R A , Kamping , E J , Jansen , E A M , Vink-Borger , M E , Popp , I , Lang , A , Spier , I , Hueneburg , R , James , P A , Li , N , Staninova , M , Lindsay , H , Cockburn , D , Spasic-Boskovic , O , Clendenning , M , Sweet , K , Capella , G , Sjursen , W , Hoberg-Vetti , H , Jongmans , M C , Neveling , K , van Kessel , A G , Morreau , H , Hes , F J , Sijmons , R H , Schackert , H K , Ruiz-Ponte , C , Dymerska , D , Lubinski , J , Rivera , B , Foulkes , W D , Tomlinson , I P , Valle , L , Buchanan , D D , Kenwrick , S , Adlard , J , Dimovski , A J , Campbell , I G , Aretz , S & Kuiper , R P 2019 , ' Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype ' , Cancer cell , vol. 35 , no. 2 , pp. 256-266.e5 . https://doi.org/10.1016/j.ccell.2018.12.011 ; ISSN:1535-610....  , 2019
 
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13

SNP association study in PMS2-associated Lynch syndrome:

Ten Broeke, Sanne W ; Elsayed, Fadwa A ; Pagan, Lisa...
Ten Broeke , S W , Elsayed , F A , Pagan , L , Olderode-Berends , M J W , Garcia , E G , Gille , H J P , van Hest , L P , Letteboer , T G W , van der Kolk , L E , Mensenkamp , A R , van Os , T A , Spruijt , L , Redeker , B J W , Suerink , M , Vos , Y J , Wagner , A , Wijnen , J T , Steyerberg , E W , Tops , C M J , van Wezel , T & Nielsen , M 2018 , ' SNP association study in PMS2-associated Lynch syndrome ' , Familial Cancer , vol. 17 , no. 4 , pp. 507-515 . https://doi.org/10.1007/s10689-017-0061-3.  , 2018
 
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