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

Year Number of Results
1993 2
2016 3
2017 2
2018 2
2019 4
2020 6
2021 6
2022 8
2023 7
2024 2

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39 results

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Page 1
Imprinting disorders.
Eggermann T, Monk D, de Nanclares GP, Kagami M, Giabicani E, Riccio A, Tümer Z, Kalish JM, Tauber M, Duis J, Weksberg R, Maher ER, Begemann M, Elbracht M. Eggermann T, et al. Among authors: duis j. Nat Rev Dis Primers. 2023 Jun 29;9(1):33. doi: 10.1038/s41572-023-00443-4. Nat Rev Dis Primers. 2023. PMID: 37386011 Review.
A multidisciplinary approach and consensus statement to establish standards of care for Angelman syndrome.
Duis J, Nespeca M, Summers J, Bird L, Bindels-de Heus KGCB, Valstar MJ, de Wit MY, Navis C, Ten Hooven-Radstaake M, van Iperen-Kolk BM, Ernst S, Dendrinos M, Katz T, Diaz-Medina G, Katyayan A, Nangia S, Thibert R, Glaze D, Keary C, Pelc K, Simon N, Sadhwani A, Heussler H, Wheeler A, Woeber C, DeRamus M, Thomas A, Kertcher E, DeValk L, Kalemeris K, Arps K, Baym C, Harris N, Gorham JP, Bohnsack BL, Chambers RC, Harris S, Chambers HG, Okoniewski K, Jalazo ER, Berent A, Bacino CA, Williams C, Anderson A. Duis J, et al. Mol Genet Genomic Med. 2022 Mar;10(3):e1843. doi: 10.1002/mgg3.1843. Epub 2022 Feb 11. Mol Genet Genomic Med. 2022. PMID: 35150089 Free PMC article. Review.
Schinzel-Giedion Syndrome.
Duis J, van Bon BWM. Duis J, et al. 2024 Mar 7. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2024 Mar 7. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 38452171 Free Books & Documents. Review.
SETBP1 Haploinsufficiency Disorder.
Morgan A, Srivastava S, Duis J, van Bon B. Morgan A, et al. Among authors: duis j. 2021 Nov 18. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2021 Nov 18. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 34807554 Free Books & Documents. Review.
Prader-Willi syndrome: an update.
Duis J. Duis J. Curr Opin Pulm Med. 2023 Nov 1;29(6):539-542. doi: 10.1097/MCP.0000000000001018. Epub 2023 Sep 12. Curr Opin Pulm Med. 2023. PMID: 37700664
Quantitative measures of motor development in Angelman syndrome.
Duis J, Skinner A, Carson R, Gouelle A, Annoussamy M, Silverman JL, Apkon S, Servais L, Carollo J. Duis J, et al. Am J Med Genet A. 2023 Jul;191(7):1711-1721. doi: 10.1002/ajmg.a.63192. Epub 2023 Apr 5. Am J Med Genet A. 2023. PMID: 37019838
Neuropsychiatric features of Prader-Willi syndrome.
Shelkowitz E, Gantz MG, Ridenour TA, Scheimann AO, Strong T, Bohonowych J, Duis J. Shelkowitz E, et al. Among authors: duis j. Am J Med Genet A. 2022 May;188(5):1457-1463. doi: 10.1002/ajmg.a.62662. Epub 2022 Jan 30. Am J Med Genet A. 2022. PMID: 35098642
A Primer on a Comprehensive Genetic Approach to Vascular Anomalies.
Borst AJ, Nakano TA, Blei F, Adams DM, Duis J. Borst AJ, et al. Among authors: duis j. Front Pediatr. 2020 Oct 19;8:579591. doi: 10.3389/fped.2020.579591. eCollection 2020. Front Pediatr. 2020. PMID: 33194911 Free PMC article. Review.
39 results