A citation-based method for searching scientific literature

Maria Pettersson, Heli Viljakainen, Petra Loid, Taina Mustila, Minna Pekkinen, Miriam Armenio, Johanna C Andersson-Assarsson, Outi Mäkitie, Anna Lindstrand. J Clin Endocrinol Metab 2017
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


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
17

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
524
17

TIDDIT, an efficient and comprehensive structural variant caller for massive parallel sequencing data.
Jesper Eisfeldt, Francesco Vezzi, Pall Olason, Daniel Nilsson, Anna Lindstrand. F1000Res 2017
31
17

SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population.
Adam Ameur, Johan Dahlberg, Pall Olason, Francesco Vezzi, Robert Karlsson, Marcel Martin, Johan Viklund, Andreas Kusalananda Kähäri, Pär Lundin, Huiwen Che,[...]. Eur J Hum Genet 2017
84
17


Large, rare chromosomal deletions associated with severe early-onset obesity.
Elena G Bochukova, Ni Huang, Julia Keogh, Elana Henning, Carolin Purmann, Kasia Blaszczyk, Sadia Saeed, Julian Hamilton-Shield, Jill Clayton-Smith, Stephen O'Rahilly,[...]. Nature 2010
343
17

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.
Angelo Scuteri, Serena Sanna, Wei-Min Chen, Manuela Uda, Giuseppe Albai, James Strait, Samer Najjar, Ramaiah Nagaraja, Marco Orrú, Gianluca Usala,[...]. PLoS Genet 2007
17


Osteogenesis imperfecta.
Antonella Forlino, Joan C Marini. Lancet 2016
381
11

PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants.
A J Kämpe, A Costantini, R E Mäkitie, N Jäntti, H Valta, M Mäyränpää, H Kröger, M Pekkinen, F Taylan, H Jiao,[...]. Osteoporos Int 2017
22
11

The Ensembl Variant Effect Predictor.
William McLaren, Laurent Gil, Sarah E Hunt, Harpreet Singh Riat, Graham R S Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham. Genome Biol 2016
11

Impaired bone health and asymptomatic vertebral compressions in fracture-prone children: a case-control study.
Mervi K Mäyränpää, Heli T Viljakainen, Sanna Toiviainen-Salo, Pentti E Kallio, Outi Mäkitie. J Bone Miner Res 2012
36
11

Nosology and classification of genetic skeletal disorders: 2015 revision.
Luisa Bonafe, Valerie Cormier-Daire, Christine Hall, Ralph Lachman, Geert Mortier, Stefan Mundlos, Gen Nishimura, Luca Sangiorgi, Ravi Savarirayan, David Sillence,[...]. Am J Med Genet A 2015
312
11

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.
Karol Estrada, Unnur Styrkarsdottir, Evangelos Evangelou, Yi-Hsiang Hsu, Emma L Duncan, Evangelia E Ntzani, Ling Oei, Omar M E Albagha, Najaf Amin, John P Kemp,[...]. Nat Genet 2012
754
11

Low Copy Number of the AMY1 Locus Is Associated with Early-Onset Female Obesity in Finland.
Heli Viljakainen, Johanna C Andersson-Assarsson, Miriam Armenio, Minna Pekkinen, Maria Pettersson, Helena Valta, Marita Lipsanen-Nyman, Outi Mäkitie, Anna Lindstrand. PLoS One 2015
50
11

Recurrent CNVs and SNVs at the NPHP1 locus contribute pathogenic alleles to Bardet-Biedl syndrome.
Anna Lindstrand, Erica E Davis, Claudia M B Carvalho, Davut Pehlivan, Jason R Willer, I-Chun Tsai, Subhadra Ramanathan, Craig Zuppan, Aniko Sabo, Donna Muzny,[...]. Am J Hum Genet 2014
53
11

Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS development in zebrafish.
Wolfgang Hofmeister, Maria Pettersson, Deniz Kurtoglu, Miriam Armenio, Jesper Eisfeldt, Nikos Papadogiannakis, Peter Gustavsson, Anna Lindstrand. Hum Mutat 2018
8
25

Intragenic duplication--a novel causative mechanism for SATB2-associated syndrome.
Agne Liedén, Malin Kvarnung, Daniel Nilssson, Ellika Sahlin, Elisabeth Syk Lundberg. Am J Med Genet A 2014
26
11

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor.
William McLaren, Bethan Pritchard, Daniel Rios, Yuan Chen, Paul Flicek, Fiona Cunningham. Bioinformatics 2010
11

Integrative genomics viewer.
James T Robinson, Helga Thorvaldsdóttir, Wendy Winckler, Mitchell Guttman, Eric S Lander, Gad Getz, Jill P Mesirov. Nat Biotechnol 2011
11

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
11


A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
11

Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity.
Audrey E Hendricks, Elena G Bochukova, Gaëlle Marenne, Julia M Keogh, Neli Atanassova, Rebecca Bounds, Eleanor Wheeler, Vanisha Mistry, Elana Henning, Antje Körner,[...]. Sci Rep 2017
26
11

MC4R agonism promotes durable weight loss in patients with leptin receptor deficiency.
Karine Clément, Heike Biebermann, I Sadaf Farooqi, Lex Van der Ploeg, Barbara Wolters, Christine Poitou, Lia Puder, Fred Fiedorek, Keith Gottesdiener, Gunnar Kleinau,[...]. Nat Med 2018
110
11

Proopiomelanocortin Deficiency Treated with a Melanocortin-4 Receptor Agonist.
Peter Kühnen, Karine Clément, Susanna Wiegand, Oliver Blankenstein, Keith Gottesdiener, Lea L Martini, Knut Mai, Ulrike Blume-Peytavi, Annette Grüters, Heiko Krude. N Engl J Med 2016
192
11

Clinical spectrum of obesity and mutations in the melanocortin 4 receptor gene.
I Sadaf Farooqi, Julia M Keogh, Giles S H Yeo, Emma J Lank, Tim Cheetham, Stephen O'Rahilly. N Engl J Med 2003
11

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.
Aurélien Macé, Marcus A Tuke, Patrick Deelen, Kati Kristiansson, Hannele Mattsson, Margit Nõukas, Yadav Sapkota, Ursula Schick, Eleonora Porcu, Sina Rüeger,[...]. Nat Commun 2017
32
11

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
11

Genetic Variation in Kruppel like Factor 15 Is Associated with Left Ventricular Hypertrophy in Patients with Type 2 Diabetes: Discovery and Replication Cohorts.
Sheila K Patel, Bryan Wai, Chim C Lang, Daniel Levin, Colin N A Palmer, Helen M Parry, Elena Velkoska, Stephen B Harrap, Piyush M Srivastava, Louise M Burrell. EBioMedicine 2017
10
20

Klf15 orchestrates circadian nitrogen homeostasis.
Darwin Jeyaraj, Frank A J L Scheer, Jürgen A Ripperger, Saptarsi M Haldar, Yuan Lu, Domenick A Prosdocimo, Sam J Eapen, Betty L Eapen, Yingjie Cui, Ganapathi H Mahabeleshwar,[...]. Cell Metab 2012
81
11

Glucocorticoids enhance muscle endurance and ameliorate Duchenne muscular dystrophy through a defined metabolic program.
Alexander Morrison-Nozik, Priti Anand, Han Zhu, Qiming Duan, Mohamad Sabeh, Domenick A Prosdocimo, Madeleine E Lemieux, Nikolai Nordsborg, Aaron P Russell, Calum A MacRae,[...]. Proc Natl Acad Sci U S A 2015
47
11

Interventions Targeting Glucocorticoid-Krüppel-like Factor 15-Branched-Chain Amino Acid Signaling Improve Disease Phenotypes in Spinal Muscular Atrophy Mice.
Lisa M Walter, Marc-Olivier Deguise, Katharina E Meijboom, Corinne A Betts, Nina Ahlskog, Tirsa L E van Westering, Gareth Hazell, Emily McFall, Anna Kordala, Suzan M Hammond,[...]. EBioMedicine 2018
22
11

Krüppel-like factor 15: Regulator of BCAA metabolism and circadian protein rhythmicity.
Liyan Fan, Paishiun N Hsieh, David R Sweet, Mukesh K Jain. Pharmacol Res 2018
24
11

Kruppel-like factor 15 is required for the cardiac adaptive response to fasting.
Keiki Sugi, Paishiun N Hsieh, Olga Ilkayeva, Shamanthika Shelkay, Bridget Moroney, Palvir Baadh, Browning Haynes, Megan Pophal, Liyan Fan, Christopher B Newgard,[...]. PLoS One 2018
8
25



The Krüppel-like factor KLF15 regulates the insulin-sensitive glucose transporter GLUT4.
Susan Gray, Mark W Feinberg, Sarah Hull, Chay T Kuo, Masafumi Watanabe, Sucharita Sen-Banerjee, Ana DePina, Richard Haspel, Mukesh K Jain. J Biol Chem 2002
172
11

Origins and functional impact of copy number variation in the human genome.
Donald F Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T Daniel Andrews, Chris Barnes, Peter Campbell,[...]. Nature 2010
11

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen, Armand Valsesia, Noam D Beckmann,[...]. Nature 2011
266
11

A genome-wide study reveals copy number variants exclusive to childhood obesity cases.
Joseph T Glessner, Jonathan P Bradfield, Kai Wang, Nagahide Takahashi, Haitao Zhang, Patrick M Sleiman, Frank D Mentch, Cecilia E Kim, Cuiping Hou, Kelly A Thomas,[...]. Am J Hum Genet 2010
63
11

Genome-wide copy number variation analysis identifies novel candidate loci associated with pediatric obesity.
Thanuja Selvanayagam, Susan Walker, Matthew J Gazzellone, Barbara Kellam, Cheryl Cytrynbaum, Dimitri J Stavropoulos, Ping Li, Catherine S Birken, Jill Hamilton, Rosanna Weksberg,[...]. Eur J Hum Genet 2018
10
20

New Finnish growth references for children and adolescents aged 0 to 20 years: Length/height-for-age, weight-for-length/height, and body mass index-for-age.
Antti Saari, Ulla Sankilampi, Marja-Leena Hannila, Vesa Kiviniemi, Kari Kesseli, Leo Dunkel. Ann Med 2011
258
11

Novel genes involved in severe early-onset obesity revealed by rare copy number and sequence variants.
Clara Serra-Juhé, Gabriel Á Martos-Moreno, Francesc Bou de Pieri, Raquel Flores, Juan R González, Benjamín Rodríguez-Santiago, Jesús Argente, Luis A Pérez-Jurado. PLoS Genet 2017
20
11

Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.
Eleanor Wheeler, Ni Huang, Elena G Bochukova, Julia M Keogh, Sarah Lindsay, Sumedha Garg, Elana Henning, Hannah Blackburn, Ruth J F Loos, Nick J Wareham,[...]. Nat Genet 2013
194
11

A genome-wide association study identifies multiple loci associated with mathematics ability and disability.
S J Docherty, O S P Davis, Y Kovas, E L Meaburn, P S Dale, S A Petrill, L C Schalkwyk, R Plomin. Genes Brain Behav 2010
51
5

PLS3 mutations in X-linked osteoporosis with fractures.
Fleur S van Dijk, M Carola Zillikens, Dimitra Micha, Markus Riessland, Carlo L M Marcelis, Christine E de Die-Smulders, Janine Milbradt, Anton A Franken, Arjan J Harsevoort, Klaske D Lichtenbelt,[...]. N Engl J Med 2013
122
5


Osteogenesis Imperfecta Type I Caused by COL1A1 Deletions.
Ghalib Bardai, Emmanuelle Lemyre, Pierre Moffatt, Telma Palomo, Francis H Glorieux, Joanna Tung, Leanne Ward, Frank Rauch. Calcif Tissue Int 2016
17
5

A novel splice mutation in PLS3 causes X-linked early onset low-turnover osteoporosis.
Christine M Laine, Maija Wessman, Sanna Toiviainen-Salo, Mari A Kaunisto, Mervi K Mäyränpää, Tero Laine, Minna Pekkinen, Heikki Kröger, Ville-Valtteri Välimäki, Matti J Välimäki,[...]. J Bone Miner Res 2015
47
5


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.