Similar articles for PMID: 16380913

Year	Number of Results
1949	1
1997	1
1998	1
1999	3
2000	3
2001	5
2002	3
2003	5
2004	6
2005	8
2006	11
2007	3
2008	7
2009	8
2010	25
2011	18
2012	16
2013	16
2014	14
2015	11
2016	11
2017	5
2018	10
2019	14
2020	14
2021	17
2022	10
2023	3
2024	0

1

Comparative genomics and gene expression analysis identifies BBS9, a new Bardet-Biedl syndrome gene.

Nishimura DY, Swiderski RE, Searby CC, Berg EM, Ferguson AL, Hennekam R, Merin S, Weleber RG, Biesecker LG, Stone EM, Sheffield VC. Nishimura DY, et al. Am J Hum Genet. 2005 Dec;77(6):1021-33. doi: 10.1086/498323. Epub 2005 Oct 26. Am J Hum Genet. 2005. PMID: 16380913 Free PMC article.

2

Delineating the Spectrum of Genetic Variants Associated with Bardet-Biedl Syndrome in Consanguineous Pakistani Pedigrees.

Rao AR, Nazir A, Imtiaz S, Paracha SA, Waryah YM, Ujjan ID, Anwar I, Iqbal A, Santoni FA, Shah I, Gul K, Baig HMA, Waryah AM, Antonarakis SE, Ansar M. Rao AR, et al. Genes (Basel). 2023 Feb 3;14(2):404. doi: 10.3390/genes14020404. Genes (Basel). 2023. PMID: 36833331 Free PMC article.

3

Adipose tissue function and insulin sensitivity in syndromic obesity of Bardet-Biedl syndrome.

Baig S, Wanninayake S, Foggensteiner L, Elhassan YS, Manolopoulos K, Ali S, Lassen PB, Clément K, Steeds RP, Tomlinson JW, Geberhiwot T. Baig S, et al. Int J Obes (Lond). 2023 May;47(5):382-390. doi: 10.1038/s41366-023-01280-x. Epub 2023 Feb 20. Int J Obes (Lond). 2023. PMID: 36807608

4

Bardet-Biedl Syndrome: Current Perspectives and Clinical Outlook.

Melluso A, Secondulfo F, Capolongo G, Capasso G, Zacchia M. Melluso A, et al. Ther Clin Risk Manag. 2023 Jan 30;19:115-132. doi: 10.2147/TCRM.S338653. eCollection 2023. Ther Clin Risk Manag. 2023. PMID: 36741589 Free PMC article. Review.

5

Prenatal diagnosis of Bardet‑Biedl syndrome due to novel variants in the BBS10 gene in a fetus with multiple anomalies: A case report.

Dong X, Li Z, Wang D, Xiong Y, Li H, Yang P, Lao L, Man T, Gan Y. Dong X, et al. Exp Ther Med. 2022 Oct 18;24(6):721. doi: 10.3892/etm.2022.11657. eCollection 2022 Dec. Exp Ther Med. 2022. PMID: 36340607 Free PMC article.

6

Novel mutations in BBS genes and clinical characterization of Chinese families with Bardet-Biedl syndrome.

Tao T, Liu J, Wang B, Pang J, Li X, Huang L. Tao T, et al. Eur J Ophthalmol. 2022 Nov 3:11206721221136324. doi: 10.1177/11206721221136324. Online ahead of print. Eur J Ophthalmol. 2022. PMID: 36325687

7

Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.

Yuan B, Schulze KV, Assia Batzir N, Sinson J, Dai H, Zhu W, Bocanegra F, Fong CT, Holder J, Nguyen J, Schaaf CP, Yang Y, Bi W, Eng C, Shaw C, Lupski JR, Liu P. Yuan B, et al. Genome Med. 2022 Sep 30;14(1):113. doi: 10.1186/s13073-022-01113-y. Genome Med. 2022. PMID: 36180924 Free PMC article.

8

Multi-Omics Studies Unveil Extraciliary Functions of BBS10 and Show Metabolic Aberrations Underlying Renal Disease in Bardet-Biedl Syndrome.

Marchese E, Caterino M, Fedele R, Pirozzi F, Cevenini A, Gupta N, Ingrosso D, Perna A, Capasso G, Ruoppolo M, Zacchia M. Marchese E, et al. Int J Mol Sci. 2022 Aug 20;23(16):9420. doi: 10.3390/ijms23169420. Int J Mol Sci. 2022. PMID: 36012682 Free PMC article.

9

Novel homozygous nonsense mutation associated with Bardet-Biedl syndrome in fetuses with congenital renal malformation.

Cai M, Lin M, Lin N, Xu L, Huang H. Cai M, et al. Medicine (Baltimore). 2022 Aug 12;101(32):e30003. doi: 10.1097/MD.0000000000030003. Medicine (Baltimore). 2022. PMID: 35960079 Free PMC article.

10

Novel Mutations in the MKKS, BBS7, and ALMS1 Genes in Iranian Children with Clinically Suspected Bardet-Biedl Syndrome.

Dehghan R, Behnam M, Salehi M, Kelishadi R. Dehghan R, et al. Case Rep Ophthalmol Med. 2022 Jul 21;2022:6110775. doi: 10.1155/2022/6110775. eCollection 2022. Case Rep Ophthalmol Med. 2022. PMID: 35912300 Free PMC article.

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