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For: Salehi Karlslätt K, Pettersson M, Jäntti N, Szafranski P, Wester T, Husberg B, Ullberg U, Stankiewicz P, Nordgren A, Lundin J, Lindstrand A, Nordenskjöld A. Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation. Mol Genet Genomic Med 2019;7:e549. [PMID: 30632303 DOI: 10.1002/mgg3.549] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Kato K, Hansen L, Clausen H. Polypeptide N-acetylgalactosaminyltransferase-Associated Phenotypes in Mammals. Molecules 2021;26:5504. [PMID: 34576978 DOI: 10.3390/molecules26185504] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
2 Jacinto JGP, Häfliger IM, Gentile A, Drögemüller C. A Heterozygous Missense Variant in MAP2K2 in a Stillborn Romagnola Calf with Skeletal-Cardio-Enteric Dysplasia. Animals (Basel) 2021;11:1931. [PMID: 34209498 DOI: 10.3390/ani11071931] [Reference Citation Analysis]
3 Lavillaureix A, Foulon G, Launay E, Belaud-Rotureau MA, Thibault R, Lambe C, Aussel D, Pasquier L, Odent S, Arnaud A, Habonimana E, Dabadie A, Jaillard S. Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities. Clin Res Hepatol Gastroenterol 2020;:101562. [PMID: 33208297 DOI: 10.1016/j.clinre.2020.10.007] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
4 Ilian A, Motoc A, Balulescu L, Secosan C, Grigoras D, Pirtea L. A Case Report of Left Atrial Isomerism in a Syndromic Context. Genes (Basel) 2020;11:E1211. [PMID: 33081203 DOI: 10.3390/genes11101211] [Reference Citation Analysis]
5 Mouron-Hryciuk J, Stoppa-Vaucher S, Busiah K, Bouthors T, Antoniou MC, Jacot E, Brusgaard K, Christesen HT, Hussain K, Dwyer A, Roth-Kleiner M, Hauschild M. Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8. Ann Pediatr Endocrinol Metab 2021;26:60-5. [PMID: 32871644 DOI: 10.6065/apem.2040042.021] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Winberg J, Gustavsson P, Sahlin E, Larsson M, Ehrén H, Fossum M, Wester T, Nordgren A, Nordenskjöld A. Pathogenic copy number variants are detected in a subset of patients with gastrointestinal malformations. Mol Genet Genomic Med 2020;8:e1084. [PMID: 31837127 DOI: 10.1002/mgg3.1084] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
7 Salehi Karlslätt K, Pettersson M, Jäntti N, Szafranski P, Wester T, Husberg B, Ullberg U, Stankiewicz P, Nordgren A, Lundin J, Lindstrand A, Nordenskjöld A. Rare copy number variants contribute pathogenic alleles in patients with intestinal malrotation. Mol Genet Genomic Med 2019;7:e549. [PMID: 30632303 DOI: 10.1002/mgg3.549] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]