Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1997 1
1998 1
2001 1
2002 1
2005 1
2007 1
2008 1
2009 1
2010 2
2011 4
2013 2
2014 3
2015 3
2016 5
2017 1
2018 2
2019 4
2020 3
2021 5
2022 9
2023 8
2024 2

Text availability

Article attribute

Article type

Publication date

Search Results

51 results

Results by year

Filters applied: . Clear all
Page 1
Similarity-based reasoning in conceptual spaces.
Douven I, Verheyen S, Elqayam S, Gärdenfors P, Osta-Vélez M. Douven I, et al. Among authors: verheyen s. Front Psychol. 2023 Sep 5;14:1234483. doi: 10.3389/fpsyg.2023.1234483. eCollection 2023. Front Psychol. 2023. PMID: 37731876 Free PMC article.
An autosomal-dominant childhood-onset disorder associated with pathogenic variants in VCP.
Mah-Som AY, Daw J, Huynh D, Wu M, Creekmore BC, Burns W, Skinner SA, Holla ØL, Smeland MF, Planes M, Uguen K, Redon S, Bierhals T, Scholz T, Denecke J, Mensah MA, Sczakiel HL, Tichy H, Verheyen S, Blatterer J, Schreiner E, Thies J, Lam C, Spaeth CG, Pena L, Ramsey K, Narayanan V, Seaver LH, Rodriguez D, Afenjar A, Burglen L, Lee EB, Chou TF, Weihl CC, Shinawi MS. Mah-Som AY, et al. Among authors: verheyen s. Am J Hum Genet. 2023 Nov 2;110(11):1959-1975. doi: 10.1016/j.ajhg.2023.10.007. Epub 2023 Oct 25. Am J Hum Genet. 2023. PMID: 37883978
A community-sourced glossary of open scholarship terms.
Parsons S, Azevedo F, Elsherif MM, Guay S, Shahim ON, Govaart GH, Norris E, O'Mahony A, Parker AJ, Todorovic A, Pennington CR, Garcia-Pelegrin E, Lazić A, Robertson O, Middleton SL, Valentini B, McCuaig J, Baker BJ, Collins E, Fillon AA, Lonsdorf TB, Lim MC, Vanek N, Kovacs M, Roettger TB, Rishi S, Miranda JF, Jaquiery M, Stewart SLK, Agostini V, Stewart AJ, Izydorczak K, Ashcroft-Jones S, Hartmann H, Ingham M, Yamada Y, Vasilev MR, Dechterenko F, Albayrak-Aydemir N, Yang YF, LaPlume AA, Wolska JK, Henderson EL, Zaneva M, Farrar BG, Mounce R, Kalandadze T, Li W, Xiao Q, Ross RM, Yeung SK, Liu M, Vandegrift ML, Kekecs Z, Topor MK, Baum MA, Williams EA, Assaneea AA, Bret A, Cashin AG, Ballou N, Dumbalska T, Kern BMJ, Melia CR, Arendt B, Vineyard GH, Pickering JS, Evans TR, Laverty C, Woodward EA, Moreau D, Roche DG, Rinke EM, Reid G, Garcia-Garzon E, Verheyen S, Kocalar HE, Blake AR, Cockcroft JP, Micheli L, Bret BB, Flack ZM, Szaszi B, Weinmann M, Lecuona O, Schmidt B, Ngiam WX, Mendes AB, Francis S, Gall BJ, Paul M, Keating CT, Grose-Hodge M, Bartlett JE, Iley BJ, Spitzer L, Pownall M, Graham CJ, Wingen T, Terry J, Oliveira CMF, Millager RA, Fox KJ, AlDoh A, Hart A, van den… See abstract for full author list ➔ Parsons S, et al. Among authors: verheyen s. Nat Hum Behav. 2022 Mar;6(3):312-318. doi: 10.1038/s41562-021-01269-4. Nat Hum Behav. 2022. PMID: 35190714 Free article. No abstract available.
Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy.
Voisin N, Schnur RE, Douzgou S, Hiatt SM, Rustad CF, Brown NJ, Earl DL, Keren B, Levchenko O, Geuer S, Verheyen S, Johnson D, Zarate YA, Hančárová M, Amor DJ, Bebin EM, Blatterer J, Brusco A, Cappuccio G, Charrow J, Chatron N, Cooper GM, Courtin T, Dadali E, Delafontaine J, Del Giudice E, Doco M, Douglas G, Eisenkölbl A, Funari T, Giannuzzi G, Gruber-Sedlmayr U, Guex N, Heron D, Holla ØL, Hurst ACE, Juusola J, Kronn D, Lavrov A, Lee C, Lorrain S, Merckoll E, Mikhaleva A, Norman J, Pradervand S, Prchalová D, Rhodes L, Sanders VR, Sedláček Z, Seebacher HA, Sellars EA, Sirchia F, Takenouchi T, Tanaka AJ, Taska-Tench H, Tønne E, Tveten K, Vitiello G, Vlčková M, Uehara T, Nava C, Yalcin B, Kosaki K, Donnai D, Mundlos S, Brunetti-Pierri N, Chung WK, Reymond A. Voisin N, et al. Among authors: verheyen s. Am J Hum Genet. 2021 May 6;108(5):857-873. doi: 10.1016/j.ajhg.2021.04.001. Am J Hum Genet. 2021. PMID: 33961779 Free PMC article.
Revealing Criterial Vagueness in Inconsistencies.
Verheyen S, White A, Égré P. Verheyen S, et al. Open Mind (Camb). 2019 Jun;3:41-51. doi: 10.1162/opmi_a_00025. Open Mind (Camb). 2019. PMID: 31517174 Free PMC article.
Teaching open and reproducible scholarship: a critical review of the evidence base for current pedagogical methods and their outcomes.
Pownall M, Azevedo F, König LM, Slack HR, Evans TR, Flack Z, Grinschgl S, Elsherif MM, Gilligan-Lee KA, de Oliveira CMF, Gjoneska B, Kalandadze T, Button K, Ashcroft-Jones S, Terry J, Albayrak-Aydemir N, Děchtěrenko F, Alzahawi S, Baker BJ, Pittelkow MM, Riedl L, Schmidt K, Pennington CR, Shaw JJ, Lüke T, Makel MC, Hartmann H, Zaneva M, Walker D, Verheyen S, Cox D, Mattschey J, Gallagher-Mitchell T, Branney P, Weisberg Y, Izydorczak K, Al-Hoorie AH, Creaven AM, Stewart SLK, Krautter K, Matvienko-Sikar K, Westwood SJ, Arriaga P, Liu M, Baum MA, Wingen T, Ross RM, O'Mahony A, Bochynska A, Jamieson M, Tromp MV, Yeung SK, Vasilev MR, Gourdon-Kanhukamwe A, Micheli L, Konkol M, Moreau D, Bartlett JE, Clark K, Brekelmans G, Gkinopoulos T, Tyler SL, Röer JP, Ilchovska ZG, Madan CR, Robertson O, Iley BJ, Guay S, Sladekova M, Sadhwani S; FORRT. Pownall M, et al. Among authors: verheyen s. R Soc Open Sci. 2023 May 17;10(5):221255. doi: 10.1098/rsos.221255. eCollection 2023 May. R Soc Open Sci. 2023. PMID: 37206965 Free PMC article. Review.
Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency.
Verheyen S, Blatterer J, Speicher MR, Bhavani GS, Boons GJ, Ilse MB, Andrae D, Sproß J, Vaz FM, Kircher SG, Posch-Pertl L, Baumgartner D, Lübke T, Shah H, Al Kaissi A, Girisha KM, Plecko B. Verheyen S, et al. J Med Genet. 2022 Oct;59(10):957-964. doi: 10.1136/jmedgenet-2021-108061. Epub 2021 Dec 16. J Med Genet. 2022. PMID: 34916232 Free PMC article.
Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring.
Nagy D, Verheyen S, Wigby KM, Borovikov A, Sharkov A, Slegesky V, Larson A, Fagerberg C, Brasch-Andersen C, Kibæk M, Bader I, Hernan R, High FA, Chung WK, Schieving JH, Behunova J, Smogavec M, Laccone F, Witsch-Baumgartner M, Zobel J, Duba HC, Weis D. Nagy D, et al. Among authors: verheyen s. Genes (Basel). 2022 Jan 15;13(1):154. doi: 10.3390/genes13010154. Genes (Basel). 2022. PMID: 35052493 Free PMC article.
51 results