Läer, L.
712  Ergebnisse:
Personensuche X
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1

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh R ; Lahrouchi N ; Tadros R...
info:eu-repo/semantics/altIdentifier/pmid/32893267.  , 2021
 
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2

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh R ; Lahrouchi N ; Tadros R...
info:eu-repo/semantics/altIdentifier/pmid/32893267.  , 2021
 
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3

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh, R ; Lahrouchi, N ; Tadros, R...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-020-00946-5.  , 2021
 
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4

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh, R ; Lahrouchi, N ; Tadros, R...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-020-00946-5.  , 2021
 
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5

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh, R ; Lahrouchi, N ; Tadros, R...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-020-00946-5.  , 2021
 
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6

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh, R ; Lahrouchi, N ; Tadros, R...
https://openaccess.sgul.ac.uk/id/eprint/112371/3/s41436-020-00946-5.pdf.  , 2021
 
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7

A human importin-β-related disorder: Syndromic thoracic aor..:

Van Gucht, I ; Meester, JAN ; Bento, JR...
https://discovery.ucl.ac.uk/id/eprint/10158793/1/A%20human%20importin%20related%20disorder.pdf.  , 2021
 
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9

Enhancing rare variant interpretation in inherited arrhythm..:

Walsh, R ; Lahrouchi, N ; Tadros, R...
https://discovery.ucl.ac.uk/id/eprint/10112002/1/Lambiase_Enhancing%20rare%20variant%20interpretation%20in%20inherited%20arrhythmias%20through%20quantitative%20analysis%20of%20consortium%20disease%20cohorts%20and%20population%20controls_AOP.pdf.  , 2020
 
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12

Elucidating the genetic architecture of Adams-Oliver syndro..:

Meester, JAN ; Sukalo, M ; Schröder, KC...
https://openaccess.sgul.ac.uk/id/eprint/109915/7/Meester_et_al-2018-Human_Mutation.pdf.  , 2018
 
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13

A mutation update on the LDS-associated genes TGFB2/3 and S..:

Schepers, D ; Tortora, G ; Morisaki, H...
Schepers , D , Tortora , G , Morisaki , H , MacCarrick , G , Lindsay , M , Liang , D , Mehta , SG , Hague , J , Verhagen , J , De Graaf - van de Laar , I , Wessels , M , Detisch , Y , van Haelst , M , Baas , A , Lichtenbelt , K , Braun , K , Linde , D , Roos - Hesselink , J , McGillivray , G , Meester , J , Maystadt , I , Coucke , P , El-Khoury , E , Parkash , S , Diness , B , Risom , L , Scurr , I , Hilhorst-Hofstee , Y , Morisaki , T , Richer , J , Desir , J , Kempers , M , Rideout , AL , Horne , G , Bennett , C , Rahikkala , E , Vandeweyer , G , Alaerts , M , Verstraeten , A , Dietz , H , Van Laer , L & Loeys , B 2018 , ' A mutation update on the LDS-associated genes TGFB2/3 and SMAD2/3 ' , Human Mutation , vol. 39 , no. 5 , pp. 621-634 . https://doi.org/10.1002/humu.23407.  , 2018
 
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14

Loss-of-function mutations in the X-linked biglycan gene ca..:

Meester, J.A ; Vandeweyer, G ; Pintelon, I...
info:eu-repo/semantics/altIdentifier/doi/10.1038/gim.2016.126.  , 2017
 
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15

Candidate Gene Resequencing in a Large Bicuspid Aortic Valv..:

Gillis, E ; Kumar, AA ; Luyckx, I...
Gillis , E , Kumar , AA , Luyckx , I , Preuss , C , Cannaerts , E , van de Beek , G , Wieschendorf , B , Alaerts , M , Bolar , N , Vandeweyer , G , Meester , J , Wunnemann , F , Gould , RA , Zhurayev , R , Zerbino , D , Mohamed , SA , Mital , S , Mertens , L , Bjorck , HM , Franco-Cereceda , A , McCallion , AS , Van Laer , L , Verhagen , J , De Graaf - van de Laar , I , Wessels , M , Messas , E , Goudot , G , Nemcikova , M , Krebsova , A , Kempers , M , Salemink , S , Duijnhouwer , T , Jeunemaitre , X , Albuisson , J , Eriksson , P , Andelfinger , G , Dietz , HC , Verstraeten , A & Loeys , BL 2017 , ' Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor ' , Frontiers in Physiology , vol. 8 , 400 . https://doi.org/10.3389/fphys.2017.00400.  , 2017
 
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