Reynares E - Search Results

Year	Number of Results
1992	1
1993	6
1994	4
1995	2
1996	5
1997	1
1998	2
1999	4
2000	2
2001	1
2002	2
2004	3
2005	5
2006	7
2007	3
2008	2
2009	1
2010	1
2011	3
2012	2
2014	2
2015	1
2016	5
2017	4
2018	2
2019	3
2021	1
2024	3
2025	1

1

RNU4-2-Related Neurodevelopmental Disorder Is Associated With a Recognisable Facial Gestalt.

Rosenblum J, Beysen D, Jansen AC, De Rademaeker M, Reyniers E, Janssens K, Meuwissen M. Rosenblum J, et al. Among authors: reyniers e. Clin Genet. 2025 Jan;107(1):104-112. doi: 10.1111/cge.14628. Epub 2024 Oct 21. Clin Genet. 2025. PMID: 39434505

2

Burden re-analysis of neurodevelopmental disorder cohorts for prioritization of candidate genes.

Smal N, Majdoub F, Janssens K, Reyniers E, Meuwissen MEC, Ceulemans B, Northrup H, Hill JB, Liu L, Errichiello E, Gana S, Strong A, Rohena L, Franciskovich R, Murali CN, Huybrechs A, Sulem T, Fridriksdottir R, Sulem P, Stefansson K, Bai Y, Rosenfeld JA, Lalani SR, Streff H; Undiagnosed Diseases Network; Kooy RF, Weckhuysen S. Smal N, et al. Among authors: reyniers e. Eur J Hum Genet. 2024 Nov;32(11):1378-1386. doi: 10.1038/s41431-024-01661-4. Epub 2024 Jul 4. Eur J Hum Genet. 2024. PMID: 38965372

3

Subtelomeric rearrangements in the mentally retarded: a comparison of detection methods.

Rooms L, Reyniers E, Kooy RF. Rooms L, et al. Among authors: reyniers e. Hum Mutat. 2005 Jun;25(6):513-24. doi: 10.1002/humu.20185. Hum Mutat. 2005. PMID: 15880643 Review.

4

PLCB1 epileptic encephalopathies; Review and expansion of the phenotypic spectrum.

Schoonjans AS, Meuwissen M, Reyniers E, Kooy F, Ceulemans B. Schoonjans AS, et al. Among authors: reyniers e. Eur J Paediatr Neurol. 2016 May;20(3):474-9. doi: 10.1016/j.ejpn.2016.01.002. Epub 2016 Jan 13. Eur J Paediatr Neurol. 2016. PMID: 26818157 Review.

5

Restoring the phenotype of fragile X syndrome: insight from the mouse model.

Gantois I, Bakker CE, Reyniers E, Willemsen R, D'Hooge R, De Deyn PP, Oostra BA, Kooy RF. Gantois I, et al. Among authors: reyniers e. Curr Mol Med. 2001 Sep;1(4):447-55. doi: 10.2174/1566524013363492. Curr Mol Med. 2001. PMID: 11899089 Review.

6

The Genetic Puzzle of Cerebral Palsy: Results of a Monocentric Study.

Thys L, Beysen D, Ceulemans B, Kenis S, Dielman C, Roelens F, Reyniers E, Mateiu L, Janssens K, Meuwissen M. Thys L, et al. Among authors: reyniers e. Pediatr Neurol. 2024 Dec;161:1-8. doi: 10.1016/j.pediatrneurol.2024.07.019. Epub 2024 Aug 5. Pediatr Neurol. 2024. PMID: 39213953

7

Clinical report of a pure subtelomeric 1qter deletion in a boy with mental retardation and multiple anomalies adds further evidence for a specific phenotype.

van Bever Y, Rooms L, Laridon A, Reyniers E, van Luijk R, Scheers S, Wauters J, Kooy RF. van Bever Y, et al. Among authors: reyniers e. Am J Med Genet A. 2005 May 15;135(1):91-5. doi: 10.1002/ajmg.a.30695. Am J Med Genet A. 2005. PMID: 15822126 Review.

8

A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.

Courtens W, Wuyts W, Scheers S, Van Luijk R, Reyniers E, Rooms L, Ceulemans B, Kooy F, Wauters J. Courtens W, et al. Among authors: reyniers e. Eur J Med Genet. 2006 Sep-Oct;49(5):402-13. doi: 10.1016/j.ejmg.2006.01.001. Epub 2006 Jan 30. Eur J Med Genet. 2006. PMID: 16488200 Review.

9

Familial hypertryptasemia with associated mast cell activation syndrome.

Sabato V, Van De Vijver E, Hagendorens M, Vrelust I, Reyniers E, Fransen E, Bridts C, De Clerck L, Mortier G, Valent P, Ebo D. Sabato V, et al. Among authors: reyniers e. J Allergy Clin Immunol. 2014 Dec;134(6):1448-1450.e3. doi: 10.1016/j.jaci.2014.06.007. Epub 2014 Jul 30. J Allergy Clin Immunol. 2014. PMID: 25086867 No abstract available.

10

Hypoparathyroidism-retardation-dysmorphism syndrome in a girl: A new variant not caused by a TBCE mutation--clinical report and review.

Courtens W, Wuyts W, Poot M, Szuhai K, Wauters J, Reyniers E, Eleveld M, Diaz G, Nöthen MM, Parvari R. Courtens W, et al. Among authors: reyniers e. Am J Med Genet A. 2006 Mar 15;140(6):611-7. doi: 10.1002/ajmg.a.31122. Am J Med Genet A. 2006. PMID: 16470743 Review.

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