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Author/Creator Wagner, Anja

1. A novel tissue‐based ß‐catenin gene and immunohistochemical analysis to exclude familial adenomatous polyposis among children with hepatoblastoma tumors. Issue 6 (15th February 2018)

Authors:
Dubbink, Hendrikus J.; Hollink, Iris H.I.M.; Avenca Valente, Carolina; Wang, Wenhui; Liu, Pengyu; Doukas, Michail; van Noesel, Max M.; Dinjens, Winand N.M.; Wagner, Anja; Smits, Ron
Journal:
Pediatric blood & cancer
Issue:
Volume 65:Issue 6(2018)
Page Start:
n/a
Record Type:
Journal Article
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2. Acellular vascular matrix grafts from human placenta chorion: Impact of ECM preservation on graft characteristics, protein composition and in vivo performance. (September 2018)

Authors:
Schneider, Karl H.; Enayati, Marjan; Grasl, Christian; Walter, Ingrid; Budinsky, Lubos; Zebic, Gabriel; Kaun, Christoph; Wagner, Anja; Kratochwill, Klaus; Redl, Heinz; Teuschl, Andreas H.; Podesser, Bruno K.; Bergmeister, Helga
Journal:
Biomaterials
Issue:
Volume 177(2018)
Page Start:
14
Record Type:
Journal Article
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5. Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis. Issue 1 (19th November 2013)

Authors:
Hes, Frederik J; Ruano, Dina; Nieuwenhuis, Marry; Tops, Carli M; Schrumpf, Melanie; Nielsen, Maartje; Huijts, Petra E A; Wijnen, Juul T; Wagner, Anja; García, Encarna B Gómez; Sijmons, Rolf H; Menko, Fred H; Letteboer, Tom G W; Hoogerbrugge, Nicoline; Harryvan, Jan; Kampman, Ellen; Morreau, Hans;...
Journal:
Journal of medical genetics
Issue:
Volume 51:Issue 1(2014)
Page Start:
55
Record Type:
Journal Article
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6. Combined germline pathogenic variants in FLCN and TP53 are associated with early onset renal cell carcinoma and brain tumors. Issue 2 (16th November 2022)

Authors:
van de Beek, Irma; Glykofridis, Iris E.; Wagner, Anja; den Toom, Dorine T.; Bongers, Ernie M. H. F.; van Leenders, Geert J. L. H.; Johannesma, Paul C.; Meijers‐Heijboer, Hanne E. J.; Wolthuis, Rob M. F.; van Steensel, Maurice A. M.; Dubbink, Hendrikus J.; Houweling, Arjan C.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 11:Issue 2(2023)
Page Start:
n/a
Record Type:
Journal Article
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7. Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome. Issue 11 (21st August 2016)

Authors:
van der Klift, Heleen M.; Mensenkamp, Arjen R.; Drost, Mark; Bik, Elsa C.; Vos, Yvonne J.; Gille, Hans J.J.P.; Redeker, Bert E.J.W.; Tiersma, Yvonne; Zonneveld, José B.M.; García, Encarna Gómez; Letteboer, Tom G.W.; Olderode‐Berends, Maran J.W.; van Hest, Liselotte P.; van Os, Theo A.; Verhoef, S...
Journal:
Human mutation
Issue:
Volume 37:Issue 11(2016)
Page Start:
1162
Record Type:
Journal Article
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9. Do we practice (or teach) what we preach? Developing a more inclusive learning environment to better prepare social work students for practice through improving the explorationof their different ethnicities within teaching, learning and assessment opportunities. Issue 5 (4th July 2019)

Authors:
Hollinrake, Sue; Hunt, Garfield; Dix, Heidi; Wagner, Anja
Journal:
Social work education
Issue:
Volume 38:Issue 5(2019)
Page Start:
582
Record Type:
Journal Article
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10. ERN GENTURIS tumour surveillance guidelines for individuals with neurofibromatosis type 1. (February 2023)

Authors:
Carton, Charlotte; Evans, D. Gareth; Blanco, Ignacio; Friedrich, Reinhard E.; Ferner, Rosalie E.; Farschtschi, Said; Salvador, Hector; Azizi, Amedeo A.; Mautner, Victor; Röhl, Claas; Peltonen, Sirkku; Stivaros, Stavros; Legius, Eric; Oostenbrink, Rianne; Brunet, Joan; Van Calenbergh, Frank; Cassi...
Journal:
EClinicalMedicine
Issue:
Volume 56(2023)
Page Start:
Record Type:
Journal Article
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