Maimaris, Jesmeen S
25  Ergebnisse:
Personensuche X
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1

The Genetics of Primary Immunodeficiency in Children:

Maimaris, Jesmeen S
https://discovery.ucl.ac.uk/id/eprint/10130699/1/Maimaris__thesis.pdf.  , 2021
 
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7

Biallelic deleterious germline SH2B3 variants cause a novel..:

Blombery, Piers ; Pazhakh, Vahid ; Albuquerque, Adriana S...
https://discovery.ucl.ac.uk/id/eprint/10170639/1/eJHaem%20-%202023%20-%20Blombery%20-%20Biallelic%20deleterious%20germline%20SH2B3%20variants%20cause%20a%20novel%20syndrome%20of%20myeloproliferation%20and.pdf.  , 2023
 
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8

Autosomal Dominant STAT6 Gain of Function Causes Severe Ato..:

Minskaia, Ekaterina ; Maimaris, Jesmeen ; Jenkins, Persephone...
https://discovery.ucl.ac.uk/id/eprint/10172196/1/s10875-023-01530-7.pdf.  , 2023
 
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12

Publisher Correction:Whole-genome sequencing of a sporadic ..:

Thaventhiran, James E.D ; Lango Allen, Hana ; Burren, Oliver S...
Thaventhiran , J E D , Lango Allen , H , Burren , O S , Rae , W , Greene , D , Staples , E , Zhang , Z , Farmery , J H R , Simeoni , I , Rivers , E , Maimaris , J , Penkett , C J , Stephens , J , Deevi , S V V , Sanchis-Juan , A , Gleadall , N S , Thomas , M J , Sargur , R B , Gordins , P , Baxendale , H E , Brown , M , Tuijnenburg , P , Worth , A , Hanson , S , Linger , R J , Buckland , M S , Rayner-Matthews , P J , Gilmour , K C , Samarghitean , C , Seneviratne , S L , Sansom , D M , Lynch , A G , Megy , K , Ellinghaus , E , Ellinghaus , D , Jorgensen , S F , Karlsen , T H , Stirrups , K E , Cutler , A J , Kumararatne , D S , Chandra , A , Edgar , J D M , Herwadkar , A , Cooper , N , Grigoriadou , S , Huissoon , A P , Goddard , S , Jolles , S , Schuetz , C , Boschann , F , Abbs , S , Adhya , Z , Adlard , J , Afzal , M , Ahmed , I , Ahmed , M , Ahmed , S , Aitman , T J , Alachkar , H , Alamelu , J , Alikhan , R , Allen , C E , Allen , L , Allsup , D J , Alvi , A , Ambegao....  , 2020
 
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15

Whole-genome sequencing of a sporadic primary immunodeficie..:

Thaventhiran, James E.D ; Lango Allen, Hana ; Burren, Oliver S...
Thaventhiran , J E D , Lango Allen , H , Burren , O S , Rae , W , Greene , D , Staples , E , Zhang , Z , Farmery , J H R , Simeoni , I , Rivers , E , Maimaris , J , Penkett , C J , Stephens , J , Deevi , S V V , Sanchis-Juan , A , Gleadall , N S , Thomas , M J , Sargur , R B , Gordins , P , Baxendale , H E , Brown , M , Tuijnenburg , P , Worth , A , Hanson , S , Linger , R J , Buckland , M S , Rayner-Matthews , P J , Gilmour , K C , Samarghitean , C , Seneviratne , S L , Sansom , D M , Lynch , A G , Megy , K , Ellinghaus , E , Ellinghaus , D , Jorgensen , S F , Karlsen , T H , Stirrups , K E , Cutler , A J , Kumararatne , D S , Chandra , A , Edgar , J D M , Herwadkar , A , Cooper , N , Grigoriadou , S , Huissoon , A P , Johnson , M , Thomas , D C , Wei , W & Primary Immunodeficiency Consortium for the NIHR Bioresource 2020 , ' Whole-genome sequencing of a sporadic primary immunodeficiency cohort ' , Nature , vol. 583 , no. 7814 , pp. 90-95 . https://doi.org/10.1038/s41....  , 2020
 
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