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Search Results - Swinkels, Iris J.
Search Results - Swinkels, Iris J.
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Value of routine follow‐up in oropharyngeal squamous cell cancer patients treated with curative intent
by
Brands, Maria T.
,
Swinkels, Iris J.
,
Aarts, Anne M. W. M.
,
Verbeek, André L. M.
,
Merkx, Matthias A. W.
,
Marres, Henri A. M.
,
Kaanders, Johannes H. A. M.
,
Melchers, Willem J. G.
,
Engen‐van Grunsven, Ilse
,
Takes, Robert P.
,
Geurts, Sandra M. E.
Published in
Head & neck
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Advancing early detection of autism spectrum disorder by applying an integrated two-stage screening approach
by
Oosterling, Iris J.
,
Wensing, Michel
,
Swinkels, Sophie H.
,
Van Der Gaag, Rutger Jan
,
Visser, Janne C.
,
Woudenberg, Tim
,
Minderaa, Ruud
,
Steenhuis, Mark-Peter
,
Buitelaar, Jan K.
Published in
Journal of child psychology and psychiatry
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Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples
by
Wijngaard, Robin
,
Demidov, German
,
O'Gorman, Luke
,
Corominas-Galbany, Jordi
,
Yaldiz, Burcu
,
Steyaert, Wouter
,
de Boer, Elke
,
Vissers, Lisenka E L M
,
Kamsteeg, Erik-Jan
,
Pfundt, Rolph
,
Swinkels, Hilde
,
den Ouden, Amber
,
Te Paske, Iris B A W
,
de Voer, Richarda M
,
Faivre, Laurence
,
Denommé-Pichon, Anne-Sophie
,
Duffourd, Yannis
,
Vitobello, Antonio
,
Chevarin, Martin
,
Straub, Volker
,
Töpf, Ana
,
van der Kooi, Anneke J
,
Magrinelli, Francesca
,
Rocca, Clarissa
,
Hanna, Michael G
,
Vandrovcova, Jana
,
Ossowski, Stephan
,
Laurie, Steven
,
Gilissen, Christian
Published in
European journal of human genetics : EJHG
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Comparative Analysis of Three Screening Instruments for Autism Spectrum Disorder in Toddlers at High Risk
by
Oosterling, Iris J.
,
Swinkels, Sophie H.
,
van der Gaag, Rutger Jan
,
Visser, Janne C.
,
Dietz, Claudine
,
Buitelaar, Jan K.
Published in
Journal of autism and developmental disorders
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Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples
by
Wijngaard, Robin
,
Demidov, German
,
O'Gorman, Luke
,
Corominas-Galbany, Jordi
,
Yaldiz, Burcu
,
Steyaert, Wouter
,
de Boer, Elke
,
Vissers, Lisenka E L M
,
Kamsteeg, Erik-Jan
,
Pfundt, Rolph
,
Swinkels, Hilde
,
den Ouden, Amber
,
Te Paske, Iris B A W
,
de Voer, Richarda M
,
Faivre, Laurence
,
Denommé-Pichon, Anne-Sophie
,
Duffourd, Yannis
,
Vitobello, Antonio
,
Chevarin, Martin
,
Straub, Volker
,
Töpf, Ana
,
van der Kooi, Anneke J
,
Magrinelli, Francesca
,
Rocca, Clarissa
,
Hanna, Michael G
,
Vandrovcova, Jana
,
Ossowski, Stephan
,
Laurie, Steven
,
Gilissen, Christian
Published in
European journal of human genetics : EJHG
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Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients
by
Swinkels, Maurice
,
Atiq, Ferdows
,
Bürgisser, Petra E.
,
Moort, Iris
,
Meijer, Karina
,
Eikenboom, Jeroen
,
Fijnvandraat, Karin
,
Galen, Karin P. M.
,
Meris, Joke
,
Schols, Saskia E. M.
,
Bom, Johanna G.
,
Cnossen, Marjon H.
,
Voorberg, Jan
,
Leebeek, Frank W. G.
,
Bierings, Ruben
,
Jansen, A. J. Gerard
,
Fijnvandraat, K.
,
Coppens, M.
,
Meris, J.
,
Nieuwenhuizen, L.
,
Meijer, K.
,
Tamminga, R. Y. J.
,
Ypma, P. F.
,
Eikenboom, H. C. J.
,
Bom, J. G.
,
Smiers, F. J. W.
,
Granzen, B.
,
Moenen, F.
,
Brons, P.
,
Schols, S. E. M.
,
Leebeek, F. W. G.
,
Cnossen, M. H.
,
Atiq, F.
,
Kwawegen, C. B.
,
Galen, K. P. M.
Published in
British journal of haematology
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Vitamin and homocysteine status of mothers and infants and the risk of nonsyndromic orofacial clefts
by
van Rooij, Iris A.L.M
,
Swinkels, Dorine W
,
Blom, Henk J
,
Merkus, Hans M.W.M
,
Steegers-Theunissen, Régine P.M
Published in
American journal of obstetrics and gynecology
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Genome-wide meta-analysis of common variant differences between men and women
by
BORASKA, Vesna
,
JERONCIC, Ana
,
BANDINELLI, Stefania
,
BARBALIC, Maja
,
BARROSO, Inês
,
BECKMANN, Jacques S
,
BIFFAR, Reiner
,
BOOMSMA, Dorret
,
CAMPBELL, Harry
,
CORRE, Tanguy
,
ERDMANN, Jeanette
,
ESKO, Tõnu
,
COLONNA, Vincenza
,
FISCHER, Krista
,
FRANCESCHINI, Nora
,
FRAYLING, Timothy M
,
GIROTTO, Giorgia
,
GONZALEZ, Juan R
,
HARRIS, Tamara B
,
HEATH, Andrew C
,
HEID, Iris M
,
HOFFMANN, Wolfgang
,
HOFMAN, Albert
,
SOUTHAM, Lorraine
,
HORIKOSHI, Momoko
,
JING HUA ZHAO
,
JACKSON, Anne U
,
HOTTENGA, Jouke-Jan
,
JULA, Antti
,
KÄHÖNEN, Mika
,
KHAW, Kay-Tee
,
KIEMENEY, Lambertus A
,
KLOPP, Norman
,
KUTALIK, Zoltán
,
NYHOLT, Dale R
,
LAGOU, Vasiliki
,
LAUNER, Lenore J
,
LEHTIMÄKI, Terho
,
LEMIRE, Mathieu
,
LOKKI, Marja-Liisa
,
LOLEY, Christina
,
LUAN, Jian'an
,
MANGINO, Massimo
,
MATEO LEACH, Irene
,
MEDLAND, Sarah E
,
WILLIAM RAYNER, Nigel
,
MIHAILOV, Evelin
,
MONTGOMERY, Grant W
,
NAVIS, Gerjan
,
NEWNHAM, John
,
NIEMINEN, Markku S
,
PALOTIE, Aarno
,
PANOUTSOPOULOU, Kalliope
,
PETERS, Annette
,
PIRASTU, Nicola
,
POLASEK, Ozren
,
PERRY, John R. B
,
TONIOLO, Daniela
,
ALBRECHT, Eva
,
WEI ANG
Published in
Human molecular genetics
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