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Lubbe, SJ
23  results:
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1

Lithium extraction from Zimbabwean petalite using ammonium ..:

Mwepu, KT ; Lubbe, SJ ; Crouse, PL
Suid-Afrikaanse Tydskrif vir Natuurwetenskap en Tegnologie.  40 (2021)  1 - p. 1-11 , 2021
Link: https://doi.org/10.36303..
 
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2

MED27 Variants Cause Developmental Delay, Dystonia, and Cer..:

Meng, L ; Isohanni, P ; Shao, Y...
https://discovery.ucl.ac.uk/id/eprint/10124204/3/Efthymiou_MED27_12302020_Annals%20of%20Neurology_clean.pdf.  , 2021
Link: https://discovery.ucl.ac..
 
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3

Assessing the Relationship Between Monoallelic PRKN Mutatio..:

Lubbe, SJ ; Bustos, B ; Hu, J...
https://discovery.ucl.ac.uk/id/eprint/10119916/1/ddaa273.pdf.  , 2021
Link: https://discovery.ucl.ac..
 
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4

Biallelic AOPEP Loss-of-Function Variants Cause Progressive..:

Zech, M ; Kumar, KR ; Reining, S...
https://discovery.ucl.ac.uk/id/eprint/10135960/1/Kurian_mds.28804.pdf.  , 2021
Link: https://discovery.ucl.ac..
 
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5

Loss-of-function variants in HOPS complex genes VPS16 and V..:

Steel, D ; Zech, M ; Zhao, C...
https://discovery.ucl.ac.uk/id/eprint/10108409/1/Barwick_ana.25879.pdf.  , 2020
Link: https://discovery.ucl.ac..
 
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6

Loss-of-Function Variants in HOPS Complex Genes VPS16 and V..:

Steel, D ; Zech, M ; Zhao, C...
https://openaccess.sgul.ac.uk/id/eprint/112563/1/ana.25879.pdf.  , 2020
Link: https://openaccess.sgul...
 
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7

A novel TBK1 mutation in a family with diverse frontotempor..:

Lamb, R ; Rohrer, JD ; Real, R...
https://discovery.ucl.ac.uk/id/eprint/10075806/8/Holton_A%20novel%20TBK1%20mutation%20in%20a%20family%20with%20diverse%20frontotemporal%20dementia%20spectrum%20disorders_VoR.pdf.  , 2019
Link: https://discovery.ucl.ac..
 
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8

Discovery and functional prioritization of Parkinson's dise..:

Jansen, IE ; Ye, H ; Heetveld, S...
doi:10.1186/s13059-017-1147-9.  , 2019
Link: https://doi.org/10.1186/..
 
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9

Discovery and functional prioritization of Parkinson's dise..:

Jansen, IE ; Ye, H ; Heetveld, S...
Genome Biol.  , 2018
Link: http://qmro.qmul.ac.uk/x..
 
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10

Parkinson's disease in GTP cyclohydrolase 1 mutation carrie..:

Mencacci, NE ; Isaias, IU ; Reich, MM...
Brain.  , 2018
Link: http://qmro.qmul.ac.uk/x..
 
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11

Discovery and functional prioritization of Parkinson's dise..:

Jansen, IE ; Ye, H ; Heetveld, S...
https://discovery.ucl.ac.uk/id/eprint/1539905/1/Ryten_art%25253A10.1186%25252Fs13059-017-1147-9.pdf.  , 2017
Link: https://discovery.ucl.ac..
 
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12

Discovery and functional prioritization of Parkinson's dise..:

Jansen, IE ; Ye, H ; Heetveld, S...
https://eprints.whiterose.ac.uk/112351/1/art%253A10.1186%252Fs13059-017-1147-9.pdf.  , 2017
Link: https://eprints.whiteros..
 
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13

Additional rare variant analysis in Parkinson's disease cas..:

Lubbe, SJ ; Escott-Price, V ; Gibbs, JR...
Human Molecular Genetics.  , 2017
Link: http://qmro.qmul.ac.uk/x..
 
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14

Early Onset Parkinson's Disease in a family of Moroccan ori..:

Norman, BP ; Lubbe, SJ ; Tan, M..
https://discovery.ucl.ac.uk/id/eprint/1570494/1/s12883-017-0933-z.pdf.  , 2017
Link: https://discovery.ucl.ac..
 
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15

Discovery and functional prioritization of Parkinson's dise..:

Jansen, IE ; Ye, H ; Heetveld, S...
Jansen , IE , Ye , H , Heetveld , S , Lechler , MC , Michels , H , Seinstra , RI , Lubbe , SJ , Drouet , V , Lesage , S , Majounie , E , Gibbs , JR , Nalls , MA , Ryten , M , Botia , JA , Vandrovcova , J , Simon-Sanchez , J , Castillo-Lizardo , M , Rizzu , P , Blauwendraat , C , Chouhan , AK , Li , YR , Yogi , P , Amin , N , Duijn , C , Morris , HR , Brice , A , Singleton , AB , David , DC , Nollen , EA , Jain , S , Shulman , JM , Heutink , P & Ipgdc 2017 , ' Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing ' , Genome Biology , vol. 18 , 22 . https://doi.org/10.1186/s13059-017-1147-9.  , 2017
Link: https://pure.eur.nl/en/p..
 
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