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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2005 1
2011 1
2012 3
2013 4
2014 3
2015 2
2016 1
2017 1
2018 2
2019 3
2020 1
2021 1
2023 1
2024 0

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Page 1
A morphogenetic EphB/EphrinB code controls hepatopancreatic duct formation.
Thestrup MI, Caviglia S, Cayuso J, Heyne RLS, Ahmad R, Hofmeister W, Satriano L, Wilkinson DG, Andersen JB, Ober EA. Thestrup MI, et al. Among authors: hofmeister w. Nat Commun. 2019 Nov 19;10(1):5220. doi: 10.1038/s41467-019-13149-7. Nat Commun. 2019. PMID: 31745086 Free PMC article.
CTNND2-a candidate gene for reading problems and mild intellectual disability.
Hofmeister W, Nilsson D, Topa A, Anderlid BM, Darki F, Matsson H, Tapia Páez I, Klingberg T, Samuelsson L, Wirta V, Vezzi F, Kere J, Nordenskjöld M, Syk Lundberg E, Lindstrand A. Hofmeister W, et al. J Med Genet. 2015 Feb;52(2):111-22. doi: 10.1136/jmedgenet-2014-102757. Epub 2014 Dec 3. J Med Genet. 2015. PMID: 25473103
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish.
Baranowska Körberg I, Hofmeister W, Markljung E, Cao J, Nilsson D, Ludwig M, Draaken M, Holmdahl G, Barker G, Reutter H, Vukojević V, Clementson Kockum C, Lundin J, Lindstrand A, Nordenskjöld A. Baranowska Körberg I, et al. Among authors: hofmeister w. Hum Mol Genet. 2015 Sep 15;24(18):5069-78. doi: 10.1093/hmg/ddv225. Epub 2015 Jun 23. Hum Mol Genet. 2015. PMID: 26105184
Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate gene.
Lundin J, Markljung E, Baranowska Körberg I, Hofmeister W, Cao J, Nilsson D, Holmdahl G, Barker G, Anderberg M, Vukojević V, Lindstrand A, Nordenskjöld A. Lundin J, et al. Among authors: hofmeister w. Mol Genet Genomic Med. 2019 Jun;7(6):e666. doi: 10.1002/mgg3.666. Epub 2019 May 1. Mol Genet Genomic Med. 2019. PMID: 31044557 Free PMC article.
21 results