Carss, Keren J
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7

MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelop..:

Reid, Kimberly M ; Spaull, Robert ; Salian, Smrithi...
https://publications.aston.ac.uk/id/eprint/45864/1/Movement_Disorders_-_2022_-_Reid_-_MED27_SLC6A7_and_MPPE1_Variants_in_a_Complex_Neurodevelopmental_Disorder_with_Severe.pdf.  , 2022
 
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9

MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelop..:

Reid, Kimberley M ; Spaull, Robert ; Salian, Smrithi...
Reid , K M , Spaull , R , Salian , S , Barwick , K , Meyer , E , Zhen , J , Hirata , H , Sheipouri , D , Benkerroum , H , Gorman , K M , Papandreou , A , Simpson , M A , Hirano , Y , Farabella , I , Topf , M , Grozeva , D , Carss , K , Smith , M , Pall , H , Lunt , P , Gressi , S D , Kamsteeg , EJ , Haack , T B , Carr , L , Guerreiro , R , Bras , J , Maher , E R , Scott , R H , Vandenberg , R J , Raymond , F L , Chong , W K , Sudhakar , S , Mankad , K , Reith , M E , Campeau , P M , Harvey , R J & Kurian , M A 2022 , ' MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia ' , Movement Disorders , vol. 37 , no. 10 , pp. 2139-2146 . https://doi.org/10.1002/mds.29147.  , 2022
 
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12

Spontaneous Coronary Artery Dissection:

Bouatia-Naji, Nabila ; Carss, Keren ; Mres, Anna...
info:eu-repo/semantics/altIdentifier/doi/10.1161/CIRCGEN.120.003030.  , 2020
 
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14

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 patients with rare diseases in a..:

Turro, Ernest ; Astle, William J ; Megy, Karyn...
Turro , E , Astle , W J , Megy , K , Gräf , S , Greene , D , Shamardina , O , Allen , H L , Sanchis-Juan , A , Frontini , M , Thys , C , Stephens , J , Mapeta , R , Burren , O S , Downes , K , Haimel , M , Tuna , S , Deevi , S V V , Aitman , T J , Bennett , D L , Calleja , P , Carss , K , Caulfield , M J , Chinnery , P F , Dixon , P H , Gale , D P , James , R , Koziell , A , Laffan , M A , Levine , A P , Maher , E R , Markus , H S , Morales , J , Morrell , N W , Mumford , A D , Ormondroyd , E , Rankin , S , Rendon , A , Richardson , S , Bennett , D L , Bueser , T , Carr-White , G , Flinter , F A , Irving , M , Josifova , D , Koziell , A , Mohammed , S N , Thomas , E , Traylor , M & Trembath , R & Williamson , C 2020 , ' Whole-genome sequencing of patients with rare diseases in a national health system ' , Nature , vol. 583 , no. 7814 , pp. 96-102 . https://doi.org/10.1038/s41586-020-2434-2.  , 2020
 
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