A citation-based method for searching scientific literature

Louise Montagne, Mehdi Derhourhi, Amélie Piton, Bénédicte Toussaint, Emmanuelle Durand, Emmanuel Vaillant, Dorothée Thuillier, Stefan Gaget, Franck De Graeve, Iandry Rabearivelo, Amélie Lansiaux, Bruno Lenne, Sylvie Sukno, Rachel Desailloud, Miriam Cnop, Ramona Nicolescu, Lior Cohen, Jean-François Zagury, Mélanie Amouyal, Jacques Weill, Jean Muller, Olivier Sand, Bruno Delobel, Philippe Froguel, Amélie Bonnefond. Mol Metab 2018
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Loss-of-function mutations in ADCY3 cause monogenic severe obesity.
Sadia Saeed, Amélie Bonnefond, Filippo Tamanini, Muhammad Usman Mirza, Jaida Manzoor, Qasim M Janjua, Sadia M Din, Julien Gaitan, Alexandra Milochau, Emmanuelle Durand,[...]. Nat Genet 2018
51
50


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
50

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
50

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
25

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
25

Novel LEPR mutations in obese Pakistani children identified by PCR-based enrichment and next generation sequencing.
Sadia Saeed, Amélie Bonnefond, Jaida Manzoor, Julien Philippe, Emmanuelle Durand, Mohsin Arshad, Olivier Sand, Taeed A Butt, Mario Falchi, Muhammad Arslan,[...]. Obesity (Silver Spring) 2014
31
25

Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.
Menachem Fromer, Jennifer L Moran, Kimberly Chambert, Eric Banks, Sarah E Bergen, Douglas M Ruderfer, Robert E Handsaker, Steven A McCarroll, Michael C O'Donovan, Michael J Owen,[...]. Am J Hum Genet 2012
331
25

Quantification of homozygosity in consanguineous individuals with autosomal recessive disease.
C Geoffrey Woods, James Cox, Kelly Springell, Daniel J Hampshire, Moin D Mohamed, Martin McKibbin, Rowena Stern, F Lucy Raymond, Richard Sandford, Saghira Malik Sharif,[...]. Am J Hum Genet 2006
174
25


Clinical and molecular genetic spectrum of congenital deficiency of the leptin receptor.
I Sadaf Farooqi, Teresia Wangensteen, Stephan Collins, Wendy Kimber, Giuseppe Matarese, Julia M Keogh, Emma Lank, Bill Bottomley, Judith Lopez-Fernandez, Ivan Ferraz-Amaro,[...]. N Engl J Med 2007
367
25

Genetic variants in LEP, LEPR, and MC4R explain 30% of severe obesity in children from a consanguineous population.
Sadia Saeed, Amélie Bonnefond, Jaida Manzoor, Faiza Shabbir, Hina Ayesha, Julien Philippe, Emmanuelle Durand, Hutokshi Crouch, Olivier Sand, Muhammad Ali,[...]. Obesity (Silver Spring) 2015
41
25

High prevalence of leptin and melanocortin-4 receptor gene mutations in children with severe obesity from Pakistani consanguineous families.
Sadia Saeed, Taeed A Butt, Mehwish Anwer, Muhammad Arslan, Philippe Froguel. Mol Genet Metab 2012
46
25

Arginylation regulates adipogenesis by regulating expression of PPARγ at transcript and protein level.
Archana Singh, Anuj Kumar Borah, Kamalakshi Deka, Akash Protim Gogoi, Kamalesh Verma, Pankaj Barah, Sougata Saha. Biochim Biophys Acta Mol Cell Biol Lipids 2019
5
25

Obesity genetics: insights from the Pakistani population.
M Pigeyre, M Saqlain, M Turcotte, G K Raja, D Meyre. Obes Rev 2018
13
25


Identification of a novel lipase gene mutated in lpd mice with hypertriglyceridemia and associated with dyslipidemia in humans.
Xiao-Yan Wen, Robert A Hegele, Jian Wang, Ding Yan Wang, Joseph Cheung, Michael Wilson, Maryam Yahyapour, Yahong Bai, Lihua Zhuang, Jennifer Skaug,[...]. Hum Mol Genet 2003
18
25

Changes in levels of peripheral hormones controlling appetite are inconsistent with hyperphagia in leptin-deficient subjects.
Sadia Saeed, Paul R Bech, Tayyaba Hafeez, Rabail Alam, Mario Falchi, Mohammad A Ghatei, Stephen R Bloom, Muhammad Arslan, Philippe Froguel. Endocrine 2014
12
25

Characterization of a novel binding partner of the melanocortin-4 receptor: attractin-like protein.
Andrea M Haqq, Patricia René, Toshiro Kishi, Kathy Khong, Charlotte E Lee, Hongyan Liu, Jeffrey M Friedman, Joel K Elmquist, Roger D Cone. Biochem J 2003
25
25

The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation.
Armand Valsesia, Aurélien Macé, Sébastien Jacquemont, Jacques S Beckmann, Zoltán Kutalik. Front Genet 2013
35
25

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
25

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
25

Homozygous null mutation of the melanocortin-4 receptor and severe early-onset obesity.
Béatrice Dubern, Selma Bisbis, Habiba Talbaoui, Johanne Le Beyec, Patrick Tounian, Jean-Marc Lacorte, Karine Clément. J Pediatr 2007
38
25

A frameshift mutation in MC4R associated with dominantly inherited human obesity.
G S Yeo, I S Farooqi, S Aminian, D J Halsall, R G Stanhope, S O'Rahilly. Nat Genet 1998
744
25

Postnatal Sim1 deficiency causes hyperphagic obesity and reduced Mc4r and oxytocin expression.
Kristen P Tolson, Terry Gemelli, Laurent Gautron, Joel K Elmquist, Andrew R Zinn, Bassil M Kublaoui. J Neurosci 2010
92
25


Subcellular localization of MC4R with ADCY3 at neuronal primary cilia underlies a common pathway for genetic predisposition to obesity.
Jacqueline E Siljee, Yi Wang, Adelaide A Bernard, Baran A Ersoy, Sumei Zhang, Aaron Marley, Mark Von Zastrow, Jeremy F Reiter, Christian Vaisse. Nat Genet 2018
82
25

A nonsense loss-of-function mutation in PCSK1 contributes to dominantly inherited human obesity.
J Philippe, P Stijnen, D Meyre, F De Graeve, D Thuillier, J Delplanque, G Gyapay, O Sand, J W Creemers, P Froguel,[...]. Int J Obes (Lond) 2015
31
25

Evidence for a strong genetic influence on childhood adiposity despite the force of the obesogenic environment.
Jane Wardle, Susan Carnell, Claire Ma Haworth, Robert Plomin. Am J Clin Nutr 2008
377
25

Leptin levels in human and rodent: measurement of plasma leptin and ob RNA in obese and weight-reduced subjects.
M Maffei, J Halaas, E Ravussin, R E Pratley, G H Lee, Y Zhang, H Fei, S Kim, R Lallone, S Ranganathan. Nat Med 1995
25

MRAP and MRAP2 are bidirectional regulators of the melanocortin receptor family.
Li F Chan, Tom R Webb, Teng-Teng Chung, Eirini Meimaridou, Sadani N Cooray, Leonardo Guasti, J Paul Chapple, Michaela Egertová, Maurice R Elphick, Michael E Cheetham,[...]. Proc Natl Acad Sci U S A 2009
138
25

The expression of genes in top obesity-associated loci is enriched in insula and substantia nigra brain regions involved in addiction and reward.
Fatou K Ndiaye, Marlène Huyvaert, Ana Ortalli, Mickaël Canouil, Cécile Lecoeur, Marie Verbanck, Stéphane Lobbens, Amna Khamis, Lorella Marselli, Piero Marchetti,[...]. Int J Obes (Lond) 2020
6
25

Loss-of-function mutations in MRAP2 are pathogenic in hyperphagic obesity with hyperglycemia and hypertension.
Morgane Baron, Julie Maillet, Marlène Huyvaert, Aurélie Dechaume, Raphaël Boutry, Hélène Loiselle, Emmanuelle Durand, Bénédicte Toussaint, Emmanuel Vaillant, Julien Philippe,[...]. Nat Med 2019
17
25

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
25

Positional cloning of the mouse obese gene and its human homologue.
Y Zhang, R Proenca, M Maffei, M Barone, L Leopold, J M Friedman. Nature 1994
25

A de novo mutation affecting human TrkB associated with severe obesity and developmental delay.
Giles S H Yeo, Chiao-Chien Connie Hung, Justin Rochford, Julia Keogh, Juliette Gray, Shoba Sivaramakrishnan, Stephen O'Rahilly, I Sadaf Farooqi. Nat Neurosci 2004
349
25

Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like features.
Amélie Bonnefond, Anne Raimondo, Fanny Stutzmann, Maya Ghoussaini, Shwetha Ramachandrappa, David C Bersten, Emmanuelle Durand, Vincent Vatin, Beverley Balkau, Olivier Lantieri,[...]. J Clin Invest 2013
64
25

Rare variants in single-minded 1 (SIM1) are associated with severe obesity.
Shwetha Ramachandrappa, Anne Raimondo, Anna M G Cali, Julia M Keogh, Elana Henning, Sadia Saeed, Amanda Thompson, Sumedha Garg, Elena G Bochukova, Soren Brage,[...]. J Clin Invest 2013
84
25

Body-mass index and all-cause mortality: individual-participant-data meta-analysis of 239 prospective studies in four continents.
Global BMI Mortality Collaboration, Emanuele Di Angelantonio, Shilpa Bhupathiraju, David Wormser, Pei Gao, Stephen Kaptoge, Amy Berrington de Gonzalez, Benjamin Cairns, Rachel Huxley, Chandra Jackson,[...]. Lancet 2016
861
25

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
25

High Prevalence of Obesity in Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) Requiring Invasive Mechanical Ventilation.
Arthur Simonnet, Mikael Chetboun, Julien Poissy, Violeta Raverdy, Jerome Noulette, Alain Duhamel, Julien Labreuche, Daniel Mathieu, Francois Pattou, Merce Jourdain. Obesity (Silver Spring) 2020
770
25

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
25


Evaluation of a melanocortin-4 receptor (MC4R) agonist (Setmelanotide) in MC4R deficiency.
Tinh-Hai Collet, Béatrice Dubern, Jacek Mokrosinski, Hillori Connors, Julia M Keogh, Edson Mendes de Oliveira, Elana Henning, Christine Poitou-Bernert, Jean-Michel Oppert, Patrick Tounian,[...]. Mol Metab 2017
84
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

Effects of recombinant leptin therapy in a child with congenital leptin deficiency.
I S Farooqi, S A Jebb, G Langmack, E Lawrence, C H Cheetham, A M Prentice, I A Hughes, M A McCamish, S O'Rahilly. N Engl J Med 1999
25

Developmental control of the melanocortin-4 receptor by MRAP2 proteins in zebrafish.
Julien A Sebag, Chao Zhang, Patricia M Hinkle, Amanda M Bradshaw, Roger D Cone. Science 2013
92
25

Loss of function of the melanocortin 2 receptor accessory protein 2 is associated with mammalian obesity.
Masato Asai, Shwetha Ramachandrappa, Maria Joachim, Yuan Shen, Rong Zhang, Nikhil Nuthalapati, Visali Ramanathan, David E Strochlic, Peter Ferket, Kirsten Linhart,[...]. Science 2013
132
25

Central nervous system control of food intake and body weight.
G J Morton, D E Cummings, D G Baskin, G S Barsh, M W Schwartz. Nature 2006
25

Brief report: impaired processing of prohormones associated with abnormalities of glucose homeostasis and adrenal function.
S O'Rahilly, H Gray, P J Humphreys, A Krook, K S Polonsky, A White, S Gibson, K Taylor, C Carr. N Engl J Med 1995
160
25


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.