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For:	van der Sanden BPGH, Schobers G, Corominas Galbany J, Koolen DA, Sinnema M, van Reeuwijk J, Stumpel CTRM, Kleefstra T, de Vries BBA, Ruiterkamp-Versteeg M, Leijsten N, Kwint M, Derks R, Swinkels H, den Ouden A, Pfundt R, Rinne T, de Leeuw N, Stegmann AP, Stevens SJ, van den Wijngaard A, Brunner HG, Yntema HG, Gilissen C, Nelen MR, Vissers LELM. The performance of genome sequencing as a first-tier test for neurodevelopmental disorders. Eur J Hum Genet 2023;31:81-8. [PMID: 36114283 DOI: 10.1038/s41431-022-01185-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]

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van der Sanden BPGH, Schobers G, Corominas Galbany J, Koolen DA, Sinnema M, van Reeuwijk J, Stumpel CTRM, Kleefstra T, de Vries BBA, Ruiterkamp-Versteeg M, Leijsten N, Kwint M, Derks R, Swinkels H, den Ouden A, Pfundt R, Rinne T, de Leeuw N, Stegmann AP, Stevens SJ, van den Wijngaard A, Brunner HG, Yntema HG, Gilissen C, Nelen MR, Vissers LELM. The performance of genome sequencing as a first-tier test for neurodevelopmental disorders. Eur J Hum Genet 2023;31:81-8. [PMID: 36114283 DOI: 10.1038/s41431-022-01185-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]

Number	Citing Articles
1	Papadopoulou E, Pepe G, Konitsiotis S, Chondrogiorgi M, Grigoriadis N, Kimiskidis VK, Tsivgoulis G, Mitsikostas DD, Chroni E, Domouzoglou E, Tsaousis G, Nasioulas G. The evolution of comprehensive genetic analysis in neurology: Implications for precision medicine. J Neurol Sci 2023;447:120609. [PMID: 36905813 DOI: 10.1016/j.jns.2023.120609] [Reference Citation Analysis]
2	Burger P, Colin F, Strehle A, Mazzucotelli T, Collot N, Coutelle R, Durand B, Bouman A, Landau Prat D, Kleefstra T, Parrend P, Piton A, Koolen DA, Mandel JL. GenIDA: an international participatory database to gain knowledge on health issues related to genetic forms of neurodevelopmental disorders. J Neural Transm (Vienna) 2023;130:459-71. [PMID: 36436153 DOI: 10.1007/s00702-022-02569-3] [Reference Citation Analysis]
3	Johannesen KM. From precision diagnosis to precision treatment in epilepsy. Nat Rev Neurol 2023;19:69-70. [PMID: 36522546 DOI: 10.1038/s41582-022-00756-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4	Li D. Genome sequencing as a single comprehensive test in molecular diagnosis. Eur J Hum Genet 2023;31:3-4. [PMID: 36289408 DOI: 10.1038/s41431-022-01215-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5	Edsjö A, Lindstrand A, Gisselsson D, Mölling P, Friedman M, Cavelier L, Johansson M, Ehrencrona H, Fagerqvist T, Strid T, Lovmar L, Jacobsson B, Johansson Å, Engstrand L, Wheelock CE, Sikora P, Wirta V, Fioretos T, Rosenquist R, Genomic Medicine Sweden (GMS). Building a precision medicine infrastructure at a national level: The Swedish experience. Camb prisms Precis med 2023;1:e15. [DOI: 10.1017/pcm.2023.3] [Reference Citation Analysis]
6	McNeill A. New year, new genes. Eur J Hum Genet 2023;31:1-2. [PMID: 36609690 DOI: 10.1038/s41431-022-01271-y] [Reference Citation Analysis]