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Nicole T M Saksens
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1

Family-based exome sequencing identifies rare coding varian..:

Ratnapriya, Rinki ; Acar, İlhan E ; Geerlings, Maartje J...
Human Molecular Genetics.  29 (2020)  12 - p. 2022-2034 , 2020
Link: https://doi.org/10.1093/..
 
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2

Identification of TP53BP2 as a Novel Candidate Gene for Pri..:

Micheal, Shazia ; Saksens, Nicole T.M. ; Hogewind, Barend F....
Molecular Neurobiology.  55 (2017)  2 - p. 1387-1395 , 2017
Link: https://doi.org/10.1007/..
 
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3

Physical Activity and Age-related Macular Degeneration: A S..:

McGuinness, Myra B. ; Le, Jerome ; Mitchell, Paul...
American Journal of Ophthalmology.  180 (2017)  - p. 29-38 , 2017
Link: https://doi.org/10.1016/..
 
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4

Whole Exome Sequencing in Patients with the Cuticular Druse..:

Duvvari, Maheswara R. ; van de Ven, Johannes P. H. ; Geerlings, Maartje J....
PLOS ONE.  11 (2016)  3 - p. e0152047 , 2016
Link: https://doi.org/10.1371/..
 
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5

Analysis of Risk Alleles and Complement Activation Levels i..:

Saksens, Nicole T. M. ; Lechanteur, Yara T. E. ; Verbakel, Sanne K....
PLOS ONE.  11 (2016)  6 - p. e0144367 , 2016
Link: https://doi.org/10.1371/..
 
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6

Mutations in CTNNA1 cause butterfly-shaped pigment dystroph..:

Saksens, Nicole T M ; Krebs, Mark P ; Schoenmaker-Koller, Frederieke E...
Nature Genetics.  48 (2015)  2 - p. 144-151 , 2015
Link: https://doi.org/10.1038/..
 
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7

Macular dystrophies mimicking age-related macular degenerat..:

Saksens, Nicole T.M. ; Fleckenstein, Monika ; Schmitz-Valckenberg, Steffen...
Progress in Retinal and Eye Research.  39 (2014)  - p. 23-57 , 2014
Link: https://doi.org/10.1016/..
 
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8

Analysis of Rare Variants in the C3 Gene in Patients with A..:

Duvvari, Maheswara R. ; Paun, Codrut C. ; Buitendijk, Gabriëlle H. S....
PLoS ONE.  9 (2014)  4 - p. e94165 , 2014
Link: https://doi.org/10.1371/..
 
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9

Smoking behaviour and attitudes in patients undergoing card..:

Saksens, Nicole T.M. ; Noyez, Luc
Interactive CardioVascular and Thoracic Surgery.  10 (2010)  2 - p. 195-199 , 2010
Link: https://doi.org/10.1510/..
 
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10

Analysis of Risk Alleles and Complement Activation Levels i..:

Nicole T M Saksens ; Yara T E Lechanteur ; Sanne K Verbakel...
http://europepmc.org/articles/PMC4892537?pdf=render.  , 2016
Link: https://doi.org/10.1371/..
 
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11

Analysis of rare variants in the C3 gene in patients with a..:

Maheswara R Duvvari ; Codrut C Paun ; Gabriëlle H S Buitendijk...
http://europepmc.org/articles/PMC3988049?pdf=render.  , 2014
Link: https://doi.org/10.1371/..
 
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12

A large genome-wide association study of age-related macula..:

Fritsche, L.G. (Lars) ; Igl, W. (Wilmar) ; Cooke Bailey, J.N. (Jessica N.)...
http://repub.eur.nl/pub/96968.  , 2016
Link: http://repub.eur.nl/pub/..
 
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13

Family-based exome sequencing identifies rare coding varian..:

Ratnapriya, Rinki ; Acar, İlhan E ; Geerlings, Maartje J...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7390936/.  , 2020
Link: http://www.ncbi.nlm.nih...
 
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14

Mutations in CTNNA1 cause butterfly-shaped pigment dystroph..:

Saksens, Nicole T.M ; Krebs, Mark P ; Schoenmaker-Koller, Frederieke E...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4787620/.  , 2015
Link: http://www.ncbi.nlm.nih...
 
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15

A large genome-wide association study of age-related macula..:

Fritsche, Lars G ; Igl, Wilmar ; Cooke Bailey, Jessica N...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4745342/.  , 2015
Link: http://www.ncbi.nlm.nih...
 
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