A citation-based method for searching scientific literature

E Geets, M E C Meuwissen, W Van Hul. Clin Genet 2019
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Rare Genetic Forms of Obesity: Clinical Approach and Current Treatments in 2016.
Hélène Huvenne, Béatrice Dubern, Karine Clément, Christine Poitou. Obes Facts 2016
59
41

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
185
33

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
101
33

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
33

An overview of mongenic and syndromic obesities in humans.
Wendy K Chung. Pediatr Blood Cancer 2012
20
25

A systematic review of genetic syndromes with obesity.
Y Kaur, R J de Souza, W T Gibson, D Meyre. Obes Rev 2017
57
25

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.
H Krude, H Biebermann, W Luck, R Horn, G Brabant, A Grüters. Nat Genet 1998
25

Pediatric Obesity-Assessment, Treatment, and Prevention: An Endocrine Society Clinical Practice Guideline.
Dennis M Styne, Silva A Arslanian, Ellen L Connor, Ismaa Sadaf Farooqi, M Hassan Murad, Janet H Silverstein, Jack A Yanovski. J Clin Endocrinol Metab 2017
278
25

Bardet-Biedl Syndrome.
Evgeny N Suspitsin, Evgeny N Imyanitov. Mol Syndromol 2016
47
25

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
264
16

New candidate loci identified by array-CGH in a cohort of 100 children presenting with syndromic obesity.
Marie-Laure Vuillaume, Sophie Naudion, Guillaume Banneau, Gwenaelle Diene, Audrey Cartault, Dorothée Cailley, Julie Bouron, Jérôme Toutain, Georges Bourrouillou, Adeline Vigouroux,[...]. Am J Med Genet A 2014
34
16

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
R G Walters, S Jacquemont, A Valsesia, A J de Smith, D Martinet, J Andersson, M Falchi, F Chen, J Andrieux, S Lobbens,[...]. Nature 2010
317
16

Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: report of novel pathogenic copy number variants.
Carla Sustek D'Angelo, Ilana Kohl, Monica Castro Varela, Cláudia Irene Emílio de Castro, Chong Ae Kim, Débora Romeo Bertola, Charles Marques Lourenço, Ana Beatriz Alvarez Perez, Celia Priszkulnik Koiffmann. Am J Med Genet A 2013
21
16

Genetics of obesity.
Lesley V Campbell Am. Aust Fam Physician 2017
9
22

Melanocortin-4 receptor in energy homeostasis and obesity pathogenesis.
Anke Hinney, Anna-Lena Volckmar, Nadja Knoll. Prog Mol Biol Transl Sci 2013
85
16

Congenital leptin deficiency is associated with severe early-onset obesity in humans.
C T Montague, I S Farooqi, J P Whitehead, M A Soos, H Rau, N J Wareham, C P Sewter, J E Digby, S N Mohammed, J A Hurst,[...]. Nature 1997
16

Genetic obesity: next-generation sequencing results of 1230 patients with obesity.
Lotte Kleinendorst, Maarten P G Massink, Mellody I Cooiman, Mesut Savas, Olga H van der Baan-Slootweg, Roosje J Roelants, Ignace C M Janssen, Hanne J Meijers-Heijboer, Nine V A M Knoers, Hans Kristian Ploos van Amstel,[...]. J Med Genet 2018
28
16

Assessment of hyperphagia in Prader-Willi syndrome.
Elisabeth M Dykens, Melissa A Maxwell, Elizabeth Pantino, Rebecca Kossler, Elizabeth Roof. Obesity (Silver Spring) 2007
81
16

Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry.
Loic Yengo, Julia Sidorenko, Kathryn E Kemper, Zhili Zheng, Andrew R Wood, Michael N Weedon, Timothy M Frayling, Joel Hirschhorn, Jian Yang, Peter M Visscher. Hum Mol Genet 2018
434
16

MYT1L mutations cause intellectual disability and variable obesity by dysregulating gene expression and development of the neuroendocrine hypothalamus.
Patricia Blanchet, Martina Bebin, Shaam Bruet, Gregory M Cooper, Michelle L Thompson, Benedicte Duban-Bedu, Benedicte Gerard, Amelie Piton, Sylvie Suckno, Charu Deshpande,[...]. PLoS Genet 2017
23
16

Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia.
Steven B Heymsfield, Nicole M Avena, Leslie Baier, Phillip Brantley, George A Bray, Lisa C Burnett, Merlin G Butler, Daniel J Driscoll, Dieter Egli, Joel Elmquist,[...]. Obesity (Silver Spring) 2014
33
16

Pathophysiology and Individualized Treatment of Hypothalamic Obesity Following Craniopharyngioma and Other Suprasellar Tumors: A Systematic Review.
Laura van Iersel, Karen E Brokke, Roger A H Adan, Lauren C M Bulthuis, Erica L T van den Akker, Hanneke M van Santen. Endocr Rev 2019
20
16

Clinical Considerations Regarding the Use of Obesity Pharmacotherapy in Adolescents with Obesity.
Gitanjali Srivastava, Claudia K Fox, Aaron S Kelly, Ania M Jastreboff, Allen F Browne, Nancy T Browne, Janey S A Pratt, Christopher Bolling, Marc P Michalsky, Stephen Cook,[...]. Obesity (Silver Spring) 2019
36
16


New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey.
P L Beales, N Elcioglu, A S Woolf, D Parker, F A Flinter. J Med Genet 1999
484
16

Modulation of blood pressure by central melanocortinergic pathways.
Jerry R Greenfield, Jeffrey W Miller, Julia M Keogh, Elana Henning, Julie H Satterwhite, Gregory S Cameron, Beatrice Astruc, John P Mayer, Soren Brage, Teik Choon See,[...]. N Engl J Med 2009
304
16

Managing Bardet-Biedl Syndrome-Now and in the Future.
Elizabeth Forsythe, Joanna Kenny, Chiara Bacchelli, Philip L Beales. Front Pediatr 2018
46
16

Patients with Bardet-Biedl syndrome have hyperleptinemia suggestive of leptin resistance.
Penelope P Feuillan, David Ng, Joan C Han, Julie C Sapp, Katie Wetsch, Emma Spaulding, Yuqian C Zheng, Rafael C Caruso, Brian P Brooks, Jennifer J Johnston,[...]. J Clin Endocrinol Metab 2011
56
16

Obesity management in Prader-Willi syndrome: current perspectives.
Antonino Crinò, Danilo Fintini, Sarah Bocchini, Graziano Grugni. Diabetes Metab Syndr Obes 2018
35
16

Bardet-Biedl syndrome.
Elizabeth Forsythe, Philip L Beales. Eur J Hum Genet 2013
263
16

Molecular basis of the obesity associated with Bardet-Biedl syndrome.
Deng-Fu Guo, Kamal Rahmouni. Trends Endocrinol Metab 2011
53
16

Future Pharmacotherapy for Obesity: New Anti-obesity Drugs on the Horizon.
Gitanjali Srivastava, Caroline Apovian. Curr Obes Rep 2018
78
16

Alström Syndrome: Mutation Spectrum of ALMS1.
Jan D Marshall, Jean Muller, Gayle B Collin, Gabriella Milan, Stephen F Kingsmore, Darrell Dinwiddie, Emily G Farrow, Neil A Miller, Francesca Favaretto, Pietro Maffei,[...]. Hum Mutat 2015
69
16

Influence of TFAP2B and KCTD15 genetic variability on personality dimensions in anorexia and bulimia nervosa.
Carmen Gamero-Villarroel, Luz M González, Raquel Rodríguez-López, David Albuquerque, Juan A Carrillo, Angustias García-Herráiz, Isalud Flores, Guillermo Gervasini. Brain Behav 2017
10
10

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
341
8

Prevalence and impact of unhealthy weight in a national sample of US adolescents with autism and other learning and behavioral disabilities.
Keydra L Phillips, Laura A Schieve, Susanna Visser, Sheree Boulet, Andrea J Sharma, Michael D Kogan, Coleen A Boyle, Marshalyn Yeargin-Allsopp. Matern Child Health J 2014
58
8

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity.
Ruxandra Bachmann-Gagescu, Heather C Mefford, Charles Cowan, Gwen M Glew, Anne V Hing, Stephanie Wallace, Patricia I Bader, Aline Hamati, Pamela J Reitnauer, Rosemarie Smith,[...]. Genet Med 2010
120
8

SH2B1 in β-cells promotes insulin expression and glucose metabolism in mice.
Zheng Chen, David L Morris, Lin Jiang, Yong Liu, Liangyou Rui. Mol Endocrinol 2014
10
10

Proximal 19q trisomy: a new syndrome of morbid obesity and mental retardation.
Amnon Zung, Shlomit Rienstein, Jenny Rosensaft, Ayala Aviram-Goldring, Zvi Zadik. Horm Res 2007
19
8

The Human Phenotype Ontology in 2017.
Sebastian Köhler, Nicole A Vasilevsky, Mark Engelstad, Erin Foster, Julie McMurry, Ségolène Aymé, Gareth Baynam, Susan M Bello, Cornelius F Boerkoel, Kym M Boycott,[...]. Nucleic Acids Res 2017
385
8

Further characterization of the new microdeletion syndrome of 16p11.2-p12.2.
Agatino Battaglia, Antonio Novelli, Laura Bernardini, Roberta Igliozzi, Barbara Parrini. Am J Med Genet A 2009
24
8


Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation.
Frank J Probst, Elizabeth R Roeder, Victoria B Enciso, Zhishuo Ou, M Lance Cooper, Patricia Eng, Jiangzhen Li, Yanghong Gu, Robert F Stratton, A Craig Chinault,[...]. Am J Med Genet A 2007
46
8

Central and peripheral control of food intake.
M M I Abdalla. Endocr Regul 2017
23
8


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
8

Genetic risk profiles for a childhood with severe overweight.
J R González, M N Estévez, P S Giralt, A Cáceres, L M L Pérez, M González-Carpio, F Ballester, J Sunyer, R Rodríguez-López. Pediatr Obes 2014
19
8

Human SH2B1 mutations are associated with maladaptive behaviors and obesity.
Michael E Doche, Elena G Bochukova, Hsiao-Wen Su, Laura R Pearce, Julia M Keogh, Elana Henning, Joel M Cline, Sadia Saeed, Anne Dale, Tim Cheetham,[...]. J Clin Invest 2012
81
8

16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2.
John C K Barber, Victoria Hall, Viv K Maloney, Shuwen Huang, Angharad M Roberts, Angela F Brady, Nicki Foulds, Beverley Bewes, Marianne Volleth, Thomas Liehr,[...]. Eur J Hum Genet 2013
22
8

Genetic variations in SEC16B, MC4R, MAP2K5 and KCTD15 were associated with childhood obesity and interacted with dietary behaviors in Chinese school-age population.
Duo Lv, Dan-Dan Zhang, Hao Wang, Yan Zhang, Li Liang, Jun-Fen Fu, Feng Xiong, Ge-Li Liu, Chun-Xiu Gong, Fei-Hong Luo,[...]. Gene 2015
24
8


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.