Dylan Gration
17  Ergebnisse:
Personensuche X
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3

An evaluation of GPT models for phenotype concept recogniti..:

Groza, Tudor ; Caufield, Harry ; Gration, Dylan...
BMC Medical Informatics and Decision Making.  24 (2024)  1 - p. , 2024
 
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8

Silver Russel syndrome in an aboriginal patient from Austra..:

Poulton, Cathryn ; Azmanov, Dimitar ; Atkinson, Vanessa...
American Journal of Medical Genetics Part A.  176 (2018)  12 - p. 2561-2563 , 2018
 
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9

Surfacing undiagnosed disease: consideration, counting and ..:

Megan F. Baxter ; Michele Hansen ; Dylan Gration..
https://www.frontiersin.org/articles/10.3389/fped.2023.1283880/full.  , 2023
 
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10

Digit-all: Rare Diseases:

Gareth Baynam ; Lynsey Chediak ; Gemma Bilkey..
https://www.emjreviews.com/innovations/article/digit-all-rare-diseases/.  , 2020
 
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11

Enabling Global Clinical Collaborations on Identifiable Pat..:

Christoffer Nellåker ; Fowzan S. Alkuraya ; Gareth Baynam...
https://www.frontiersin.org/article/10.3389/fgene.2019.00611/full.  , 2019
 
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13

Congenital anomalies in children with postneonatally acquir..:

Goldsmith, Shona ; McIntyre, Sarah ; Scott, Heather...
Goldsmith , S , McIntyre , S , Scott , H , Himmelmann , K , Smithers-Sheedy , H , Andersen , G L , Blair , E , Badawi , N , Garne , E , The Comprehensive CA-CP Study Group , Barisic , I , Bosnjak Mejaski , V , Uldall , P , Amar , E , Sellier , E , Hollung , S J , Klungsøyr , K , Braz , P , Virella , D , Gibson , C , Källén , K , Reid , S M , Baynam , G , Gration , D , Hansen , M & Watson , L 2021 , ' Congenital anomalies in children with postneonatally acquired cerebral palsy : an international data linkage study ' , Developmental Medicine and Child Neurology , vol. 63 , no. 4 , pp. 421-428 . https://doi.org/10.1111/dmcn.14805.  , 2021
 
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14

Enabling Global Clinical Collaborations on Identifiable Pat..:

Nellaker, Christoffer ; Alkuraya, Fowzan S ; Baynam, Gareth...
Nellaker , C , Alkuraya , F S , Baynam , G , Bernier , R A , Bernier , F P J , Boulangerw , V , Brudno , M , Brunner , H G , Clayton-Smith , J , Cogne , B , Dawkins , H J S , deVries , B B A , Douzgou , S , Dudding-Byth , T , Eichler , E E , Ferlaino , M , Fieggen , K , Firth , H , FitzPatrick , D R , Gration , D , Groza , T , Haende , M , Hallowel , N , Hamosh , A , Hehir-Kwa , J , Hitz , M-P , Hughes , M , Kini , U , Kleefstra , T , Kooy , R F , Krawitz , P , Kury , S , Lees , M , Lyon , G J , Lyonnet , S , Marcadier , J L , Meyn , S , Moslerova , V , Politei , J M , Poulton , C C , Raymond , F L , Reijnders , M R F , Robinson , P N , Romano , C , Rose , C M , Sainsbury , D C G , Schofield , L , Sutton , V R , Tumovec , M , Van Dijck , A , Van Esch , H , Wilkie , A O M & Minerva Consortium 2019 , ' Enabling Global Clinical Collaborations on Identifiable Patient Data : The Minerva Initiative ' , Frontiers in Genetics , vol. 10 , 611 . https://doi.org/10.3389/fgene.201....  , 2019
 
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