Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Multiple splice defects in ABCA1cause low HDL-C in a family with Hypoalphalipoproteinemia and premature coronary disease
Jeffrey Rhyne, Myrna Mantaring, DAVID F. GARDNER, et al.
BMC Medical Genetics (2009) Vol. 10, Iss. 1
Open Access | Times Cited: 65

Showing 1-25 of 65 citing articles:

Roles for retrotransposon insertions in human disease
Dustin C. Hancks, Haig H. Kazazian
Mobile DNA (2016) Vol. 7, Iss. 1
Open Access | Times Cited: 608
GRASP v2.0: an update on the Genome-Wide Repository of Associations between SNPs and phenotypes
John D. Eicher, Christa Landowski, Brian Stackhouse, et al.
Nucleic Acids Research (2014) Vol. 43, Iss. D1, pp. D799-D804
Open Access | Times Cited: 151
Whole-genome sequence–based analysis of high-density lipoprotein cholesterol
Alanna C. Morrison, Arend Voorman, Andrew D. Johnson, et al.
Nature Genetics (2013) Vol. 45, Iss. 8, pp. 899-901
Open Access | Times Cited: 135
Impaired ABCA1/ABCG1-mediated lipid efflux in the mouse retinal pigment epithelium (RPE) leads to retinal degeneration
Federica Storti, Katrin Klee, Vyara Todorova, et al.
eLife (2019) Vol. 8
Open Access | Times Cited: 85
The role of polymorphism in various potential genes on polycystic ovary syndrome susceptibility and pathogenesis
Hiral Chaudhary, Jalpa Patel, Nayan Jain, et al.
Journal of Ovarian Research (2021) Vol. 14, Iss. 1
Open Access | Times Cited: 64
From SNPs to pathways: Biological interpretation of type 2 diabetes (T2DM) genome wide association study (GWAS) results
Elisa Cirillo, Martina Kutmon, Manuel A. González Hernández, et al.
PLoS ONE (2018) Vol. 13, Iss. 4, pp. e0193515-e0193515
Open Access | Times Cited: 48
Explaining the disease phenotype of intergenic SNP through predicted long range regulation
Jingqi Chen, Weidong Tian
Nucleic Acids Research (2016) Vol. 44, Iss. 18, pp. 8641-8654
Open Access | Times Cited: 47
Mutational spectrum of the APC and MUTYH genes and genotype–phenotype correlations in Brazilian FAP, AFAP, and MAP patients
Giovana Tardin Torrezan, Felipe Cavalcanti Carneiro da Silva, Érika Maria Monteiro Santos, et al.
Orphanet Journal of Rare Diseases (2013) Vol. 8, Iss. 1
Open Access | Times Cited: 46
Tensor Factorization for Precision Medicine in Heart Failure with Preserved Ejection Fraction
Yuan Luo, Faraz S. Ahmad, Sanjiv J. Shah
Journal of Cardiovascular Translational Research (2017) Vol. 10, Iss. 3, pp. 305-312
Open Access | Times Cited: 45
Mitochondrial DNA mutations and cardiovascular disease
Alexander W. Bray, Scott W. Ballinger
Current Opinion in Cardiology (2017) Vol. 32, Iss. 3, pp. 267-274
Open Access | Times Cited: 45
Exploring the “Other” subfamily of HECT E3-ligases for therapeutic intervention
Sunil Singh, J.D. Ng, J. Sivaraman
Pharmacology & Therapeutics (2021) Vol. 224, pp. 107809-107809
Closed Access | Times Cited: 28
Effects of the PPARG P12A and C161T gene variants on serum lipids in coronary heart disease patients with and without Type 2 diabetes
Hülya Yılmaz, Özlem Kurnaz, Özlem Kar Kurt, et al.
Molecular and Cellular Biochemistry (2011) Vol. 358, Iss. 1-2, pp. 355-363
Closed Access | Times Cited: 45
Prediction of Disease and Phenotype Associations from Genome-Wide Association Studies
Stephanie N. Lewis, Elaine O. Nsoesie, Charles M. Weeks, et al.
PLoS ONE (2011) Vol. 6, Iss. 11, pp. e27175-e27175
Open Access | Times Cited: 41
The TCF7L2rs7903146 polymorphism, dietary intakes and type 2 diabetes risk in an Algerian population
Hadjira Ouhaïbi-Djellouli, Sounnia Médiène-Benchekor, Sarah Aïcha Lardjam-Hetraf, et al.
BMC Genomic Data (2014) Vol. 15, Iss. 1
Open Access | Times Cited: 36
Epidemiology and genetics of granulomatosis with polyangiitis
Pratibha Banerjee, Arushi Jain, Uma Kumar, et al.
Rheumatology International (2021) Vol. 41, Iss. 12, pp. 2069-2089
Closed Access | Times Cited: 26
ABCB1/MDR1 gene polymorphism and colorectal cancer risk: a meta‐analysis of case–control studies
Tao He, Anwei Mo, K. Zhang, et al.
Colorectal Disease (2012) Vol. 15, Iss. 1, pp. 12-18
Closed Access | Times Cited: 33
Meteorological factors, air pollutants, and emergency department visits for otitis media: a time series study
Massimo Gestro, Vincenzo Condemi, Luisella Bardi, et al.
International Journal of Biometeorology (2017) Vol. 61, Iss. 10, pp. 1749-1764
Closed Access | Times Cited: 31
Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease
Gary W. Beecham, Badri N. Vardarajan, Elizabeth Blue, et al.
Neurology Genetics (2018) Vol. 4, Iss. 6
Open Access | Times Cited: 28
Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults
Ashish Chiddarwar, Selma Z. D’Silva, Roshan Colah, et al.
Annals of Human Genetics (2016) Vol. 81, Iss. 1, pp. 11-19
Closed Access | Times Cited: 27
Late-onset combined immune deficiency associated to skin granuloma due to heterozygous compound mutations in RAG1 gene in a 14years old male
Svetlana O. Sharapova, Alexandr Migas, Irina Guryanova, et al.
Human Immunology (2012) Vol. 74, Iss. 1, pp. 18-22
Closed Access | Times Cited: 30
A novel mutation in the ABCA1 gene causing an atypical phenotype of Tangier disease
Smita Negi, Ariel Brautbar, Salim S. Virani, et al.
Journal of clinical lipidology (2012) Vol. 7, Iss. 1, pp. 82-87
Closed Access | Times Cited: 25
The nuclear factor-kB functional promoter polymorphism is associated with endometriosis and infertility
Bianca Bianco, Tatiana Goberstein Lerner, Camila Martins Trevisan, et al.
Human Immunology (2012) Vol. 73, Iss. 11, pp. 1190-1193
Closed Access | Times Cited: 24
A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large family
Marianna Maranghi, Gessica Truglio, Antonio Gallo, et al.
Biochemical and Biophysical Research Communications (2018) Vol. 508, Iss. 2, pp. 487-493
Open Access | Times Cited: 23
BLOOM: BLoom filter based oblivious outsourced matchings
Jan Henrik Ziegeldorf, Jan Pennekamp, David Hellmanns, et al.
BMC Medical Genomics (2017) Vol. 10, Iss. S2
Open Access | Times Cited: 22
New trend in colorectal cancer in Germany: are young patients at increased risk for advanced colorectal cancer?
Peter C. Ambe, Stefan Jansen, Hubert Zirngibl
World Journal of Surgical Oncology (2017) Vol. 15, Iss. 1
Open Access | Times Cited: 22
Page 1 - Next Page

Scroll to top