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:

Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population
Baoyong Sha, Tie‐Lin Yang, Lan‐Juan Zhao, et al.
Journal of Human Genetics (2009) Vol. 54, Iss. 4, pp. 199-202
Open Access | Times Cited: 85

Showing 1-25 of 85 citing articles:

Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV
J. Fah Sathirapongsasuti, Hane Lee, Basil A. Horst, et al.
Bioinformatics (2011) Vol. 27, Iss. 19, pp. 2648-2654
Open Access | Times Cited: 381

Recent progress in genetics, epigenetics and metagenomics unveils the pathophysiology of human obesity
Marie Pigeyre, Fereshteh Yazdi, Yuvreet Kaur, et al.
Clinical Science (2016) Vol. 130, Iss. 12, pp. 943-986
Open Access | Times Cited: 360

Low copy number of the salivary amylase gene predisposes to obesity
Mario Falchi, Julia S. El-Sayed Moustafa, Petros Takousis, et al.
Nature Genetics (2014) Vol. 46, Iss. 5, pp. 492-497
Open Access | Times Cited: 236

From obesity genetics to the future of personalized obesity therapy
Julia S. El-Sayed Moustafa, Philippe Froguel
Nature Reviews Endocrinology (2013) Vol. 9, Iss. 7, pp. 402-413
Open Access | Times Cited: 204

From monogenic to polygenic obesity: recent advances
Anke Hinney, Carla Ivane Ganz Vogel, Johannes Hebebrand
European Child & Adolescent Psychiatry (2010) Vol. 19, Iss. 3, pp. 297-310
Open Access | Times Cited: 235

Association of genetic variation in FTO with risk of obesity and type 2 diabetes with data from 96,551 East and South Asians
Haipeng Li, Tuomas O. Kilpeläinen, Chaolei Liu, et al.
Diabetologia (2011) Vol. 55, Iss. 4, pp. 981-995
Open Access | Times Cited: 190

Implications of gene copy-number variation in health and diseases
Suhani Almal, Harish Padh
Journal of Human Genetics (2011) Vol. 57, Iss. 1, pp. 6-13
Open Access | Times Cited: 156

The evolution and population diversity of human-specific segmental duplications
Megan Y. Dennis, Lana Harshman, Bradley J. Nelson, et al.
Nature Ecology & Evolution (2017) Vol. 1, Iss. 3
Open Access | Times Cited: 154

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis
Ivonne Jarick, Carla Ivane Ganz Vogel, Susann Scherag, et al.
Human Molecular Genetics (2010) Vol. 20, Iss. 4, pp. 840-852
Open Access | Times Cited: 127

Ethnic and population differences in the genetic predisposition to human obesity
Carolina Stryjecki, Akram Alyass, David Meyre
Obesity Reviews (2017) Vol. 19, Iss. 1, pp. 62-80
Closed Access | Times Cited: 124

Chipping Away the ‘Missing Heritability’: GIANT Steps Forward in the Molecular Elucidation of Obesity – but Still Lots to Go
Johannes Hebebrand, Anna‐Lena Volckmar, Nadja Knoll, et al.
Obesity Facts (2010) Vol. 3, Iss. 5, pp. 294-303
Open Access | Times Cited: 114

Genetics of fat tissue accumulation in pigs: a comparative approach
M. Świtoński, Monika Stachowiak, J. Cieślak, et al.
Journal of Applied Genetics (2010) Vol. 51, Iss. 2, pp. 153-168
Closed Access | Times Cited: 107

Molecular Basis of Obesity: Current Status and Future Prospects
Hélène Choquet, David Meyre
Current Genomics (2011) Vol. 12, Iss. 3, pp. 154-168
Open Access | Times Cited: 101

Ancestral paternal genotype controls body weight and food intake for multiple generations
Soha Yazbek, Sabrina H. Spiezio, Joseph H. Nadeau, et al.
Human Molecular Genetics (2010) Vol. 19, Iss. 21, pp. 4134-4144
Open Access | Times Cited: 72

Genomic disorders: A window into human gene and genome evolution
Claudia M.B. Carvalho, Feng Zhang, James R. Lupski
Proceedings of the National Academy of Sciences (2010) Vol. 107, Iss. suppl_1, pp. 1765-1771
Open Access | Times Cited: 72

Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study
Gaëlle Marenne, Benjamín Rodríguez-Santiago, Montserrat García‐Closas, et al.
Human Mutation (2010) Vol. 32, Iss. 2, pp. 240-248
Open Access | Times Cited: 68

Large Copy-Number Variations Are Enriched in Cases With Moderate to Extreme Obesity
Kai Wang, Weidong Li, Joseph Glessner, et al.
Diabetes (2010) Vol. 59, Iss. 10, pp. 2690-2694
Open Access | Times Cited: 68

Low Salivary Amylase Gene (AMY1) Copy Number Is Associated with Obesity and Gut Prevotella Abundance in Mexican Children and Adults
Paola León‐Mimila, Hugo Villamil‐Ramírez, Blanca E. López-Contreras, et al.
Nutrients (2018) Vol. 10, Iss. 11, pp. 1607-1607
Open Access | Times Cited: 43

Genetics of Adiposity in Large Animal Models for Human Obesity—Studies on Pigs and Dogs
Monika Stachowiak, Izabela Szczerbal, M. Świtoński
Progress in molecular biology and translational science (2016), pp. 233-270
Closed Access | Times Cited: 41

Copy Number Variation
Tie‐Lin Yang, Yan Guo, Christopher J. Papasian, et al.
Elsevier eBooks (2012), pp. 123-132
Closed Access | Times Cited: 43

Copy Number Variants in Obesity-Related Syndromes: Review and Perspectives on Novel Molecular Approaches
Carla S. D’Angelo, Célia Priszkulnik Koiffmann
Journal of Obesity (2012) Vol. 2012, pp. 1-15
Open Access | Times Cited: 41

Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity
Julia S. El-Sayed Moustafa, Hariklia Eleftherohorinou, Adam J. de Smith, et al.
Human Molecular Genetics (2012) Vol. 21, Iss. 16, pp. 3727-3738
Open Access | Times Cited: 41

Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity
Robin Walters, Lachlan Coin, Aimo Ruokonen, et al.
PLoS ONE (2013) Vol. 8, Iss. 3, pp. e58048-e58048
Open Access | Times Cited: 40

Analysis of Genome-Wide Copy Number Variations in Chinese Indigenous and Western Pig Breeds by 60 K SNP Genotyping Arrays
Yanan Wang, Zhonglin Tang, Yaqi Sun, et al.
PLoS ONE (2014) Vol. 9, Iss. 9, pp. e106780-e106780
Open Access | Times Cited: 35

Page 1 - Next Page

Scroll to top