BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Ipe J, Swart M, Burgess KS, Skaar TC. High-Throughput Assays to Assess the Functional Impact of Genetic Variants: A Road Towards Genomic-Driven Medicine. Clin Transl Sci 2017;10:67-77. [PMID: 28213901 DOI: 10.1111/cts.12440] [Cited by in Crossref: 25] [Cited by in F6Publishing: 22] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Sümegi A, Hendrik Z, Gáll T, Felszeghy E, Szakszon K, Antal-Szalmás P, Beke L, Papp Á, Méhes G, Balla J, Balla G. A novel splice site indel alteration in the EIF2AK3 gene is responsible for the first cases of Wolcott-Rallison syndrome in Hungary. BMC Med Genet 2020;21:61. [PMID: 32216767 DOI: 10.1186/s12881-020-0985-6] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Pacanowski MA. Translating Precision. Clin Transl Sci 2017;10:56-7. [PMID: 28106333 DOI: 10.1111/cts.12454] [Reference Citation Analysis]
3 Starita LM, Ahituv N, Dunham MJ, Kitzman JO, Roth FP, Seelig G, Shendure J, Fowler DM. Variant Interpretation: Functional Assays to the Rescue. Am J Hum Genet 2017;101:315-25. [PMID: 28886340 DOI: 10.1016/j.ajhg.2017.07.014] [Cited by in Crossref: 164] [Cited by in F6Publishing: 118] [Article Influence: 32.8] [Reference Citation Analysis]
4 Sutherland HG, Albury CL, Griffiths LR. Advances in genetics of migraine. J Headache Pain 2019;20:72. [PMID: 31226929 DOI: 10.1186/s10194-019-1017-9] [Cited by in Crossref: 36] [Cited by in F6Publishing: 27] [Article Influence: 12.0] [Reference Citation Analysis]
5 Pauly R, Ziats CA, Abenavoli L, Schwartz CE, Boccuto L. New Strategies for Clinical Trials in Autism Spectrum Disorder. Rev Recent Clin Trials 2021;16:131-7. [PMID: 33222679 DOI: 10.2174/1574887115666201120093634] [Reference Citation Analysis]
6 Meyer D, Fu BXH, Chavez M, Loeillet S, Cerqueira PG, Nicolas A, Heyer WD. Cooperation between non-essential DNA polymerases contributes to genome stability in Saccharomyces cerevisiae. DNA Repair (Amst) 2019;76:40-9. [PMID: 30818168 DOI: 10.1016/j.dnarep.2019.02.004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
7 Guo DF, Rahmouni K. The Bardet-Biedl syndrome protein complex regulates cell migration and tissue repair through a Cullin-3/RhoA pathway. Am J Physiol Cell Physiol 2019;317:C457-65. [PMID: 31216194 DOI: 10.1152/ajpcell.00498.2018] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
8 Russell LE, Zhou Y, Almousa AA, Sodhi JK, Nwabufo CK, Lauschke VM. Pharmacogenomics in the era of next generation sequencing - from byte to bedside. Drug Metab Rev 2021;53:253-78. [PMID: 33820459 DOI: 10.1080/03602532.2021.1909613] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Raraigh KS, Han ST, Davis E, Evans TA, Pellicore MJ, McCague AF, Joynt AT, Lu Z, Atalar M, Sharma N, Sheridan MB, Sosnay PR, Cutting GR. Functional Assays Are Essential for Interpretation of Missense Variants Associated with Variable Expressivity. Am J Hum Genet 2018;102:1062-77. [PMID: 29805046 DOI: 10.1016/j.ajhg.2018.04.003] [Cited by in Crossref: 40] [Cited by in F6Publishing: 35] [Article Influence: 10.0] [Reference Citation Analysis]
10 Göblös A, Varga E, Farkas K, Árvai K, Kemény L. Genetic Investigation of Inverse Psoriasis. Life (Basel) 2021;11:654. [PMID: 34357026 DOI: 10.3390/life11070654] [Reference Citation Analysis]
11 Chakravorty S, Hegde M. Inferring the effect of genomic variation in the new era of genomics. Hum Mutat 2018;39:756-73. [PMID: 29633501 DOI: 10.1002/humu.23427] [Cited by in Crossref: 15] [Cited by in F6Publishing: 12] [Article Influence: 3.8] [Reference Citation Analysis]
12 Sophocleous F, Milano EG, Pontecorboli G, Chivasso P, Caputo M, Rajakaruna C, Bucciarelli-Ducci C, Emanueli C, Biglino G. Enlightening the Association between Bicuspid Aortic Valve and Aortopathy. J Cardiovasc Dev Dis 2018;5:E21. [PMID: 29671812 DOI: 10.3390/jcdd5020021] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 1.5] [Reference Citation Analysis]
13 Xiao F, Guo S, Yang F, Zhao L, Wang L. MDM2 and its functional polymorphism SNP309 contribute to the development of esophageal carcinoma. J Gene Med 2019;21:e3086. [DOI: 10.1002/jgm.3086] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
14 Xiao F, Zhang P, Wang Y, Tian Y, James M, Huang CC, Wang L, Wang L. Single-nucleotide polymorphism rs13426236 contributes to an increased prostate cancer risk via regulating MLPH splicing variant 4. Mol Carcinog 2020;59:45-55. [PMID: 31659808 DOI: 10.1002/mc.23127] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
15 Penzar DD, Zinkevich AO, Vorontsov IE, Sitnik VV, Favorov AV, Makeev VJ, Kulakovskiy IV. What Do Neighbors Tell About You: The Local Context of Cis-Regulatory Modules Complicates Prediction of Regulatory Variants. Front Genet 2019;10:1078. [PMID: 31737053 DOI: 10.3389/fgene.2019.01078] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
16 Wanke KA, Devanna P, Vernes SC. Understanding Neurodevelopmental Disorders: The Promise of Regulatory Variation in the 3'UTRome. Biol Psychiatry 2018;83:548-57. [PMID: 29289333 DOI: 10.1016/j.biopsych.2017.11.006] [Cited by in Crossref: 23] [Cited by in F6Publishing: 18] [Article Influence: 4.6] [Reference Citation Analysis]
17 Weinberg SM, Cornell R, Leslie EJ. Craniofacial genetics: Where have we been and where are we going? PLoS Genet 2018;14:e1007438. [PMID: 29927928 DOI: 10.1371/journal.pgen.1007438] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 3.5] [Reference Citation Analysis]
18 Lauschke VM, Ingelman-Sundberg M. Prediction of drug response and adverse drug reactions: From twin studies to Next Generation Sequencing. Eur J Pharm Sci 2019;130:65-77. [PMID: 30684656 DOI: 10.1016/j.ejps.2019.01.024] [Cited by in Crossref: 20] [Cited by in F6Publishing: 16] [Article Influence: 6.7] [Reference Citation Analysis]
19 Whitworth J, Smith PS, Martin JE, West H, Luchetti A, Rodger F, Clark G, Carss K, Stephens J, Stirrups K, Penkett C, Mapeta R, Ashford S, Megy K, Shakeel H, Ahmed M, Adlard J, Barwell J, Brewer C, Casey RT, Armstrong R, Cole T, Evans DG, Fostira F, Greenhalgh L, Hanson H, Henderson A, Hoffman J, Izatt L, Kumar A, Kwong A, Lalloo F, Ong KR, Paterson J, Park SM, Chen-Shtoyerman R, Searle C, Side L, Skytte AB, Snape K, Woodward ER, Tischkowitz MD, Maher ER; NIHR BioResource Rare Diseases Consortium. Comprehensive Cancer-Predisposition Gene Testing in an Adult Multiple Primary Tumor Series Shows a Broad Range of Deleterious Variants and Atypical Tumor Phenotypes. Am J Hum Genet 2018;103:3-18. [PMID: 29909963 DOI: 10.1016/j.ajhg.2018.04.013] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 6.3] [Reference Citation Analysis]
20 Hammond CL, Willoughby JM, Parker MJ. Genomics for paediatricians: promises and pitfalls. Arch Dis Child 2018;103:895-900. [DOI: 10.1136/archdischild-2017-314558] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
21 Russell LE, Zhou Y, Lauschke VM, Kim RB. In Vitro Functional Characterization and in Silico Prediction of Rare Genetic Variation in the Bile Acid and Drug Transporter, Na + -Taurocholate Cotransporting Polypeptide (NTCP, SLC10A1 ). Mol Pharmaceutics 2020;17:1170-81. [DOI: 10.1021/acs.molpharmaceut.9b01200] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 3.0] [Reference Citation Analysis]
22 Sivadas A, Scaria V. Population-scale genomics-Enabling precision public health. Adv Genet 2019;103:119-61. [PMID: 30904093 DOI: 10.1016/bs.adgen.2018.09.001] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
23 Ipe J, Collins KS, Hao Y, Gao H, Bhatia P, Gaedigk A, Liu Y, Skaar TC. PASSPORT-seq: A Novel High-Throughput Bioassay to Functionally Test Polymorphisms in Micro-RNA Target Sites. Front Genet 2018;9:219. [PMID: 29963077 DOI: 10.3389/fgene.2018.00219] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
24 Weinberg SM, Roosenboom J, Shaffer JR, Shriver MD, Wysocka J, Claes P. Hunting for genes that shape human faces: Initial successes and challenges for the future. Orthod Craniofac Res 2019;22 Suppl 1:207-12. [PMID: 31074157 DOI: 10.1111/ocr.12268] [Cited by in Crossref: 7] [Cited by in F6Publishing: 4] [Article Influence: 2.3] [Reference Citation Analysis]