Manole, Andreea
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1

Interfacing Aptamer-Modified Nanopipettes with Neuronal Med..:

Stuber, Annina ; Cavaccini, Anna ; Manole, Andreea...
info:eu-repo/semantics/altIdentifier/doi/10.1021/acsmeasuresciau.3c00047.  , 2024
 
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Bi-allelic LETM1 variants perturb mitochondrial ion homeost..:

Kaiyrzhanov, Rauan ; Mohammed, Sami E.M ; Maroofian, Reza...
https://www.sciencedirect.com/science/article/pii/S0002929722003111?via%3Dihub.  , 2023
 
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3

HLA-DRB1*1501 influences long-term disability progression a..:

Brownlee, Wallace J ; Tur, Carmen ; Manole, Andreea...
https://discovery.ucl.ac.uk/id/eprint/10161915/1/CCiccarelli__WALLACE_IS%20Genetics_Paper_MSJ_Final_References_Main%20text_Revision_tracked%20changes%5B38%5D-OC.pdf.  , 2022
 
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5

Bi-allelic LETM1 variants perturb mitochondrial ion homeost..:

Kaiyrzhanov, Rauan ; Mohammed, Sami EM ; Maroofian, Reza...
https://discovery.ucl.ac.uk/id/eprint/10155215/1/Bi-allelic%20LETM1%20variants%20perturb%20mitochondrial%20ion%20homeostasis.pdf.  , 2022
 
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10

De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause N..:

Manole, Andreea ; Efthymiou, Stephanie ; O'Connor, Emer...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2020.06.016.  , 2020
 
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11

De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause N..:

Manole, Andreea ; Efthymiou, Stephanie ; O'Connor, Emer...
Manole , A , Efthymiou , S , O'Connor , E , Mendes , M I , Jennings , M , Maroofian , R , Davagnanam , I , Mankad , K , Lopez , M R , Salpietro , V , Harripaul , R , Badalato , L , Walia , J , Francklyn , C S , Athanasiou-Fragkouli , A , Sullivan , R , Desai , S , Baranano , K , Zafar , F , Rana , N , Ilyas , M , Horga , A , Kara , M , Mattioli , F , Goldenberg , A , Griffin , H , Piton , A , Henderson , L B , Kara , B , Aslanger , A D , Raaphorst , J , Pfundt , R , Portier , R , Shinawi , M , Kirby , A , Christensen , K M , Wang , L , Rosti , R O , Paracha , S A , Sarwar , M T , Jenkins , D , Ahmed , J , Santoni , F A , Ranza , E , Iwaszkiewicz , J , Cytrynbaum , C , Weksberg , R , Wentzensen , I M , Guillen Sacoto , M J , Si , Y , Telegrafi , A , Andrews , M V , Baldridge , D , Gabriel , H , Mohr , J , Oehl-Jaschkowitz , B , Debard , S , Senger , B , Fischer , F , van Ravenwaaij , C , Fock , A J M , Stevens , S J C , Bähler , J , Nasar , A , Mantovani , J F , Manzur....  , 2020
 
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13

AMPA receptor GluA2 subunit defects are a cause of neurodev..:

Salpietro, Vincenzo ; Dixon, Christine L ; Guo, Hui...
Salpietro , V , Dixon , C L , Guo , H , Bello , O D , Vandrovcova , J , Efthymiou , S , Maroofian , R , Heimer , G , Burglen , L , Valence , S , Torti , E , Hacke , M , Rankin , J , Tariq , H , Colin , E , Procaccio , V , Striano , P , Mankad , K , Lieb , A , Chen , S , Pisani , L , Bettencourt , C , Männikkö , R , Manole , A , Brusco , A , Grosso , E , Ferrero , G B , Armstrong-Moron , J , Gueden , S , Bar-Yosef , O , Tzadok , M , Monaghan , K G , Santiago-Sim , T , Person , R E , Cho , M T , Willaert , R , Yoo , Y , Chae , J-H , Quan , Y , Wu , H , Wang , T , Bernier , R A , Xia , K , Blesson , A , Jain , M , Motazacker , M M , Jaeger , B , Schneider , A L , Boysen , K , Muir , A M , Llorente , C , Skabar , A , Chez , M , Choi , M , Macaya , A , Rothman , J E , Eichler , E E , Kullmann , D M , Houlden , H & SYNAPS Study Group 2019 , ' AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders ' , Nature Communications , vol. 10 , no. 1 ....  , 2019
 
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