A citation-based method for searching scientific literature

Maritha J Kotze, Hilmar K Lückhoff, Armand V Peeters, Karin Baatjes, Mardelle Schoeman, Lize van der Merwe, Kathleen A Grant, Leslie R Fisher, Nicole van der Merwe, Jacobus Pretorius, David P van Velden, Ettienne J Myburgh, Fredrieka M Pienaar, Susan J van Rensburg, Yandiswa Y Yako, Alison V September, Kelebogile E Moremi, Frans J Cronje, Nicki Tiffin, Christianne S H Bouwens, Juanita Bezuidenhout, Justus P Apffelstaedt, F Stephen Hough, Rajiv T Erasmus, Johann W Schneider. Crit Rev Clin Lab Sci 2015
Times Cited: 20







List of co-cited articles
29 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


MammaPrint Pre-screen Algorithm (MPA) reduces chemotherapy in patients with early-stage breast cancer.
Kathleen A Grant, Justus P Apffelstaedt, Colleen A Wright, Ettienne Myburgh, Rika Pienaar, Manie De Klerk, Maritha J Kotze. S Afr Med J 2013
10
30

Pathology-supported genetic testing directed at shared disease pathways for optimized health in later life.
Maritha J Kotze, David P van Velden, Karien Botha, Casper H Badenhorst, Heloise Avenant, Susan J van Rensburg, Frans J Cronjé. Per Med 2013
8
37

A survey of tools for variant analysis of next-generation genome sequencing data.
Stephan Pabinger, Andreas Dander, Maria Fischer, Rene Snajder, Michael Sperk, Mirjana Efremova, Birgit Krabichler, Michael R Speicher, Johannes Zschocke, Zlatko Trajanoski. Brief Bioinform 2014
292
15

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
15

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
15

The fat mass and obesity-associated FTO rs9939609 polymorphism is associated with elevated homocysteine levels in patients with multiple sclerosis screened for vascular risk factors.
Wiliam Davis, Susan J van Rensburg, Frans J Cronje, Lindiwe Whati, Leslie R Fisher, Lize van der Merwe, Dieter Geiger, M Shafick Hassan, Tandi Matsha, Rajiv T Erasmus,[...]. Metab Brain Dis 2014
27
10

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
10



CYP2D6 genotyping and use of antidepressants in breast cancer patients: test development for clinical application.
Nicole van der Merwe, Christianne S H Bouwens, Rika Pienaar, Lize van der Merwe, Yandiswa Y Yako, Dieter H Geiger, Maritha J Kotze. Metab Brain Dis 2012
6
33

A founder BRCA2 mutation in non-Afrikaner breast cancer patients of the Western Cape of South Africa.
N C van der Merwe, N Hamel, S-R Schneider, J P Apffelstaedt, J T Wijnen, W D Foulkes. Clin Genet 2012
19
10

Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur J Hum Genet 2016
110
10


The African Genome Variation Project shapes medical genetics in Africa.
Deepti Gurdasani, Tommy Carstensen, Fasil Tekola-Ayele, Luca Pagani, Ioanna Tachmazidou, Konstantinos Hatzikotoulas, Savita Karthikeyan, Louise Iles, Martin O Pollard, Ananyo Choudhury,[...]. Nature 2015
266
10


Personalized medicine and human genetic diversity.
Yi-Fan Lu, David B Goldstein, Misha Angrist, Gianpiero Cavalleri. Cold Spring Harb Perspect Med 2014
77
10

Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals.
Masao Nagasaki, Jun Yasuda, Fumiki Katsuoka, Naoki Nariai, Kaname Kojima, Yosuke Kawai, Yumi Yamaguchi-Kabata, Junji Yokozawa, Inaho Danjoh, Sakae Saito,[...]. Nat Commun 2015
229
10

From big data analysis to personalized medicine for all: challenges and opportunities.
Akram Alyass, Michelle Turcotte, David Meyre. BMC Med Genomics 2015
165
10

The UK10K project identifies rare variants in health and disease.
Klaudia Walter, Josine L Min, Jie Huang, Lucy Crooks, Yasin Memari, Shane McCarthy, John R B Perry, ChangJiang Xu, Marta Futema, Daniel Lawson,[...]. Nature 2015
529
10

Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.
Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, Stephen Clayton, Jeremy F McRae, Margriet van Kogelenberg, Daniel A King, Kirsty Ambridge, Daniel M Barrett, Tanya Bayzetinova,[...]. Lancet 2015
363
10

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
518
10

Physicians' preparedness for integration of genomic and pharmacogenetic testing into practice within a major healthcare system.
Christina G Selkirk, Scott M Weissman, Andy Anderson, Peter J Hulick. Genet Test Mol Biomarkers 2013
80
10


Genomic medicine: a decade of successes, challenges, and opportunities.
Jeanette J McCarthy, Howard L McLeod, Geoffrey S Ginsburg. Sci Transl Med 2013
136
10

ClinVar: public archive of relationships among sequence variation and human phenotype.
Melissa J Landrum, Jennifer M Lee, George R Riley, Wonhee Jang, Wendy S Rubinstein, Deanna M Church, Donna R Maglott. Nucleic Acids Res 2014
10

The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.
Annalisa Buniello, Jacqueline A L MacArthur, Maria Cerezo, Laura W Harris, James Hayhurst, Cinzia Malangone, Aoife McMahon, Joannella Morales, Edward Mountjoy, Elliot Sollis,[...]. Nucleic Acids Res 2019
794
10

Implementation of a breast cancer genetic service in South Africa - lessons learned.
Mardelle Schoeman, Justus P Apffelstaedt, Karin Baatjes, Michael Urban. S Afr Med J 2013
15
13

Exome Sequencing in a Family with Luminal-Type Breast Cancer Underpinned by Variation in the Methylation Pathway.
Nicole van der Merwe, Armand V Peeters, Fredrieka M Pienaar, Juanita Bezuidenhout, Susan J van Rensburg, Maritha J Kotze. Int J Mol Sci 2017
6
33

Integrating Genomics into Healthcare: A Global Responsibility.
Zornitza Stark, Lena Dolman, Teri A Manolio, Brad Ozenberger, Sue L Hill, Mark J Caulfied, Yves Levy, David Glazer, Julia Wilson, Mark Lawler,[...]. Am J Hum Genet 2019
108
10

Benefits of lifestyle modification in NAFLD.
Stephen A Harrison, Christopher Paul Day. Gut 2007
156
5


Hyaluronic acid levels can predict severe fibrosis and platelet counts can predict cirrhosis in patients with nonalcoholic fatty liver disease.
Hiroyuki Kaneda, Etsuko Hashimoto, Satoru Yatsuji, Katsutoshi Tokushige, Keiko Shiratori. J Gastroenterol Hepatol 2006
84
5

Hepatic steatosis index: a simple screening tool reflecting nonalcoholic fatty liver disease.
Jeong-Hoon Lee, Donghee Kim, Hwa Jung Kim, Chang-Hoon Lee, Jong In Yang, Won Kim, Yoon Jun Kim, Jung-Hwan Yoon, Sang-Heon Cho, Myung-Whun Sung,[...]. Dig Liver Dis 2010
371
5

Paradoxical lower serum triglyceride levels and higher type 2 diabetes mellitus susceptibility in obese individuals with the PNPLA3 148M variant.
Colin N A Palmer, Cristina Maglio, Carlo Pirazzi, Maria Antonella Burza, Martin Adiels, Lindsay Burch, Louise A Donnelly, Helen Colhoun, Alexander S Doney, John F Dillon,[...]. PLoS One 2012
59
5


Association of HFE and TMPRSS6 genetic variants with iron and erythrocyte parameters is only in part dependent on serum hepcidin concentrations.
Michela Traglia, Domenico Girelli, Ginevra Biino, Natascia Campostrini, Michela Corbella, Cinzia Sala, Corrado Masciullo, Fiammetta Viganò, Iwan Buetti, Giorgio Pistis,[...]. J Med Genet 2011
66
5

Carotid intima-media thickness is predicted by combined eotaxin levels and severity of hepatic steatosis at ultrasonography in obese patients with Nonalcoholic Fatty Liver Disease.
Giovanni Tarantino, Susan Costantini, Carmine Finelli, Francesca Capone, Eliana Guerriero, Nicolina La Sala, Saverio Gioia, Giuseppe Castello. PLoS One 2014
23
5

Fatty liver index correlates with non-alcoholic fatty liver disease, but not with newly diagnosed coronary artery atherosclerotic disease in Chinese patients.
Zhao-Yan Jiang, Chen-Ying Xu, Xian-Xing Chang, Wei-Wei Li, Lu-Ying Sun, Xiao-Bo Yang, Li-Fen Yu. BMC Gastroenterol 2013
18
5

Alanine aminotransferase as a marker of non-alcoholic fatty liver disease in relation to type 2 diabetes mellitus and cardiovascular disease.
Roger K Schindhelm, Michaela Diamant, Jacqueline M Dekker, Maarten E Tushuizen, Tom Teerlink, Robert J Heine. Diabetes Metab Res Rev 2006
210
5

Controlled attenuation parameter for the detection and quantification of hepatic steatosis in nonalcoholic fatty liver disease.
Wah-Kheong Chan, Nik Raihan Nik Mustapha, Sanjiv Mahadeva. J Gastroenterol Hepatol 2014
93
5



Treatment of non-alcoholic fatty liver disease.
Jessica Dyson, Chris Day. Dig Dis 2014
31
5


PNPLA3 is regulated by glucose in human hepatocytes, and its I148M mutant slows down triglyceride hydrolysis.
Julia Perttilä, Carolina Huaman-Samanez, Sandrine Caron, Kimmo Tanhuanpää, Bart Staels, Hannele Yki-Järvinen, Vesa M Olkkonen. Am J Physiol Endocrinol Metab 2012
56
5

Noninvasive biomarkers for the diagnosis of steatohepatitis and advanced fibrosis in NAFLD.
Steven G Pearce, Nirav C Thosani, Jen-Jung Pan. Biomark Res 2013
56
5

Ferritin levels and risk of metabolic syndrome: meta-analysis of observational studies.
Victoria Abril-Ulloa, Gemma Flores-Mateo, Rosa Solà-Alberich, Begoña Manuel-y-Keenoy, Victoria Arija. BMC Public Health 2014
43
5

A feed-forward loop amplifies nutritional regulation of PNPLA3.
Yongcheng Huang, Shaoqing He, John Zhong Li, Young-Kyo Seo, Timothy F Osborne, Jonathan C Cohen, Helen H Hobbs. Proc Natl Acad Sci U S A 2010
238
5

Is aspartate aminotransferase-to-platelet ratio index a biomarker in the evaluation of advanced fibrosis in non-alcoholic fatty liver disease?
Mehmet Agilli, Fevzi Nuri Aydin, Tuncer Cayci, Yasemin Gulcan Kurt. Gastroenterol Rep (Oxf) 2014
1
100



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.