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

Year Number of Results
1982 2
1983 2
1984 4
1985 5
1986 6
1987 8
1988 9
1989 8
1990 4
1991 8
1992 13
1993 6
1994 7
1995 9
1996 19
1997 14
1998 19
1999 20
2000 11
2001 15
2002 15
2003 13
2004 12
2005 19
2006 24
2007 26
2008 24
2009 16
2010 22
2011 18
2012 18
2013 28
2014 17
2015 22
2016 14
2017 18
2018 21
2019 9
2020 13
2021 18
2022 13
2023 7
2024 7
2025 7
2026 1

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535 results

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Page 1
Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement.
Lacombe D, Bloch-Zupan A, Bredrup C, Cooper EB, Houge SD, García-Miñaúr S, Kayserili H, Larizza L, Lopez Gonzalez V, Menke LA, Milani D, Saettini F, Stevens CA, Tooke L, Van der Zee JA, Van Genderen MM, Van-Gils J, Waite J, Adrien JL, Bartsch O, Bitoun P, Bouts AHM, Cueto-González AM, Dominguez-Garrido E, Duijkers FA, Fergelot P, Halstead E, Huisman SA, Meossi C, Mullins J, Nikkel SM, Oliver C, Prada E, Rei A, Riddle I, Rodriguez-Fonseca C, Rodríguez Pena R, Russell J, Saba A, Santos-Simarro F, Simpson BN, Smith DF, Stevens MF, Szakszon K, Taupiac E, Totaro N, Valenzuena Palafoll I, Van Der Kaay DCM, Van Wijk MP, Vyshka K, Wiley S, Hennekam RC. Lacombe D, et al. Among authors: van der zee ja. J Med Genet. 2024 May 21;61(6):503-519. doi: 10.1136/jmg-2023-109438. J Med Genet. 2024. PMID: 38471765 Free PMC article. Review.
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis.
Kleinberger G, Yamanishi Y, Suárez-Calvet M, Czirr E, Lohmann E, Cuyvers E, Struyfs H, Pettkus N, Wenninger-Weinzierl A, Mazaheri F, Tahirovic S, Lleó A, Alcolea D, Fortea J, Willem M, Lammich S, Molinuevo JL, Sánchez-Valle R, Antonell A, Ramirez A, Heneka MT, Sleegers K, van der Zee J, Martin JJ, Engelborghs S, Demirtas-Tatlidede A, Zetterberg H, Van Broeckhoven C, Gurvit H, Wyss-Coray T, Hardy J, Colonna M, Haass C. Kleinberger G, et al. Among authors: van der zee j. Sci Transl Med. 2014 Jul 2;6(243):243ra86. doi: 10.1126/scitranslmed.3009093. Sci Transl Med. 2014. PMID: 24990881
Cervical cancer.
van der Zee J, Franckena M. van der Zee J, et al. Int J Hyperthermia. 2012;28(6):475-7. doi: 10.3109/02656736.2012.714050. Int J Hyperthermia. 2012. PMID: 22906108 Free article. No abstract available.
Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia.
Manzoni C, Kia DA, Ferrari R, Leonenko G, Costa B, Saba V, Jabbari E, Tan MM, Albani D, Alvarez V, Alvarez I, Andreassen OA, Angiolillo A, Arighi A, Baker M, Benussi L, Bessi V, Binetti G, Blackburn DJ, Boada M, Boeve BF, Borrego-Ecija S, Borroni B, Bråthen G, Brooks WS, Bruni AC, Caroppo P, Bandres-Ciga S, Clarimon J, Colao R, Cruchaga C, Danek A, de Boer SC, de Rojas I, di Costanzo A, Dickson DW, Diehl-Schmid J, Dobson-Stone C, Dols-Icardo O, Donizetti A, Dopper E, Durante E, Ferrari C, Forloni G, Frangipane F, Fratiglioni L, Kramberger MG, Galimberti D, Gallucci M, García-González P, Ghidoni R, Giaccone G, Graff C, Graff-Radford NR, Grafman J, Halliday GM, Hernandez DG, Hjermind LE, Hodges JR, Holloway G, Huey ED, Illán-Gala I, Josephs KA, Knopman DS, Kristiansen M, Kwok JB, Leber I, Leonard HL, Libri I, Lleo A, Mackenzie IR, Madhan GK, Maletta R, Marquié M, Maver A, Menendez-Gonzalez M, Milan G, Miller BL, Morris CM, Morris HR, Nacmias B, Newton J, Nielsen JE, Nilsson C, Novelli V, Padovani A, Pal S, Pasquier F, Pastor P, Perneczky R, Peterlin B, Petersen RC, Piguet O, Pijnenburg YA, Puca AA, Rademakers R, Rainero I, Reus LM, Richardson AM, Riemenschneider M, Rogaeva E, Rogelj… See abstract for full author list ➔ Manzoni C, et al. Among authors: van der zee j. Am J Hum Genet. 2024 Jul 11;111(7):1316-1329. doi: 10.1016/j.ajhg.2024.05.017. Epub 2024 Jun 17. Am J Hum Genet. 2024. PMID: 38889728 Free PMC article.
Genotype-phenotype links in frontotemporal lobar degeneration.
Van Mossevelde S, Engelborghs S, van der Zee J, Van Broeckhoven C. Van Mossevelde S, et al. Among authors: van der zee j. Nat Rev Neurol. 2018 Jun;14(6):363-378. doi: 10.1038/s41582-018-0009-8. Nat Rev Neurol. 2018. PMID: 29777184 Review.
Today's patients.
van der Zee J. van der Zee J. Future Oncol. 2005 Dec;1(6):711-4. doi: 10.2217/14796694.1.6.711. Future Oncol. 2005. PMID: 16556048 No abstract available.
Modifiers of GRN-Associated Frontotemporal Lobar Degeneration.
Wauters E, Van Mossevelde S, Van der Zee J, Cruts M, Van Broeckhoven C. Wauters E, et al. Among authors: van der zee j. Trends Mol Med. 2017 Oct;23(10):962-979. doi: 10.1016/j.molmed.2017.08.004. Epub 2017 Sep 7. Trends Mol Med. 2017. PMID: 28890134 Review.
Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of HTT associated with an early disease onset in C9orf72 carriers.
Barbier M, Gareau T, Camuzat A, Guillaud-Bataille M, Boluda S, Clot F, Araktingi L, Borroni B, van der Zee J, Ghidoni R, Bellini S, Galimberti D, Rossi G, Nacmias B, De la Casa-Fages B, Pastor P; French Clinical and Genetic Research Network on FTD/FTD-ALS and PrevDemALS Study Groups; Latouche M, le Guern E, Durr A, Laquerrière A, Moccia R, Seilhean D, Alvarez V, Le Ber I. Barbier M, et al. Among authors: van der zee j. Brain Commun. 2025 Jun 4;7(3):fcaf220. doi: 10.1093/braincomms/fcaf220. eCollection 2025. Brain Commun. 2025. PMID: 40585812 Free PMC article.
[Severe bronchial asthma].
Toutenhoofd P, van der Zee JS. Toutenhoofd P, et al. Among authors: van der zee js. Ned Tijdschr Geneeskd. 2013;157(33):A6117. Ned Tijdschr Geneeskd. 2013. PMID: 23945432 Review. Dutch.
535 results