A citation-based method for searching scientific literature

Pamela Magini, Emanuela Scarano, Ilaria Donati, Alberto Sensi, Laura Mazzanti, Annamaria Perri, Federica Tamburrino, Patrizia Mongelli, Antonio Percesepe, Paola Visconti, Antonia Parmeggiani, Marco Seri, Claudio Graziano. Gene 2019
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity



Transcriptome analysis of the Capra hircus ovary.
Zhong Quan Zhao, Li Juan Wang, Xiao Wei Sun, Jiao Jiao Zhang, Yong Ju Zhao, Ri Su Na, Jia Hua Zhang. PLoS One 2015
14
25

Effects of Wnt/β-catenin signaling on bisphenol A exposure in male mouse reproductive cells.
Zhiqi Fang, Xiaoli Liu, Xiaosi Yang, Xianbin Song, Xiaoyu Chen. Mol Med Rep 2015
12
25

Oxidative stress-related PMK-1 P38 MAPK activation as a mechanism for toxicity of silver nanoparticles to reproduction in the nematode Caenorhabditis elegans.
Dongyoung Lim, Ji-Yeon Roh, Hyun-Jeong Eom, Jeong-Yun Choi, Jinwon Hyun, Jinhee Choi. Environ Toxicol Chem 2012
78
25

[Structural variation in the human genome].
Yong-Shu He, Wen Zhang, Zhao-Qing Yang. Yi Chuan 2009
1
100

Goat PDGFRB: unique mRNA expression profile in gonad and significant association between genetic variation and litter size.
Wenjing Yang, Hailong Yan, Ke Wang, Yang Cui, Tong Zhou, Han Xu, Haijing Zhu, Jinwang Liu, Xianyong Lan, Lei Qu,[...]. R Soc Open Sci 2019
7
25

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
25

Whole-genome scanning for the litter size trait associated genes and SNPs under selection in dairy goat (Capra hircus).
Fang-Nong Lai, Hong-Li Zhai, Ming Cheng, Jun-Yu Ma, Shun-Feng Cheng, Wei Ge, Guo-Liang Zhang, Jun-Jie Wang, Rui-Qian Zhang, Xue Wang,[...]. Sci Rep 2016
49
25


Genetic Risk Factors for Poor Cognitive Development in Children With Low Birth Weight.
Lisa M Blair, Rita H Pickler, P Cristian Gugiu, Jodi L Ford, Cindy L Munro, Cindy M Anderson. Biol Res Nurs 2020
2
50

ERBB receptor feedback inhibitor 1 regulation of estrogen receptor activity is critical for uterine implantation in mice.
Tae Hoon Kim, Dong-Kee Lee, Heather L Franco, John P Lydon, Jae-Wook Jeong. Biol Reprod 2010
28
25

Gene length as a biological timer to establish temporal transcriptional regulation.
Killeen S Kirkconnell, Brian Magnuson, Michelle T Paulsen, Brian Lu, Karan Bedi, Mats Ljungman. Cell Cycle 2017
10
25

CNVcaller: highly efficient and widely applicable software for detecting copy number variations in large populations.
Xihong Wang, Zhuqing Zheng, Yudong Cai, Ting Chen, Chao Li, Weiwei Fu, Yu Jiang. Gigascience 2017
51
25

Mitochondrial sub-cellular localization of cAMP-specific phosphodiesterase 8A in ovarian follicular cells.
Amel Lounas, Nathalie Vernoux, Marc Germain, Marie-Eve Tremblay, François J Richard. Sci Rep 2019
3
33

Copy number variations in East-Asian population and their evolutionary and functional implications.
Seon-Hee Yim, Tae-Min Kim, Hae-Jin Hu, Ji-Hong Kim, Bong-Jo Kim, Jong-Young Lee, Bok-Ghee Han, Seung-Hun Shin, Seung-Hyun Jung, Yeun-Jun Chung. Hum Mol Genet 2010
61
25

Influence of cAMP modulator supplementation of in vitro culture medium on Bos taurus indicus embryos.
Camila Bortoliero Costa, Paula Alvares Lunardelli, Patricia Kubo Fontes, Mateus José Sudano, Marcelo Fábio Gouveia Nogueira, Amauri Alcindo Alfieri, Christina Ramires Ferreira, Camila Bruna de Lima, Luciana Simões Rafagnin Marinho, Marcelo Marcondes Seneda. Theriogenology 2020
2
50

Diversity of copy number variation in a worldwide population of sheep.
Liu Yang, Lingyang Xu, Yang Zhou, Mei Liu, Lei Wang, James W Kijas, Hongping Zhang, Li Li, George E Liu. Genomics 2018
26
25

A 14-bp functional deletion within the CMTM2 gene is significantly associated with litter size in goat.
Zihong Kang, Sihuan Zhang, Libang He, Haijing Zhu, Zhen Wang, Hailong Yan, Yongzhen Huang, Ruihua Dang, Chuzhao Lei, Hong Chen,[...]. Theriogenology 2019
35
25

The earliest transcribed zygotic genes are short, newly evolved, and different across species.
Patricia Heyn, Martin Kircher, Andreas Dahl, Janet Kelso, Pavel Tomancak, Alex T Kalinka, Karla M Neugebauer. Cell Rep 2014
110
25

Effects of the Oral Oxytocin Receptor Antagonist Tocolytic OBE001 on Reproduction in Rats.
Oliver Pohl, Deborah Perks, Jon Rhodes, Laura Comotto, Paul Baldrick, André Chollet. Reprod Sci 2016
4
25

Expression patterns of p38αMAPK during follicular development in the ovaries of neonatal rats.
Shifu Hu, Meng Rao, Hui Lei, Yanqing Wu, Yingying Wang, Dandan Ke, Wei Xia, Changhong Zhu. Acta Histochem 2017
5
25

GSTM1 gene expression and copy number variation in prostate cancer patients-Effect of chemical exposures and physical activity.
Antonio Gómez-Martín, Luis J Martinez-Gonzalez, Ignacio Puche-Sanz, Jose M Cozar, Jose A Lorente, Antonio F Hernández, Maria J Alvarez-Cubero. Urol Oncol 2019
4
25

Global diversity, population stratification, and selection of human copy-number variation.
Peter H Sudmant, Swapan Mallick, Bradley J Nelson, Fereydoun Hormozdiari, Niklas Krumm, John Huddleston, Bradley P Coe, Carl Baker, Susanne Nordenfelt, Michael Bamshad,[...]. Science 2015
181
25

Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development.
Yuqi Qiu, Thomas Arbogast, Sandra Martin Lorenzo, Hongying Li, Shih C Tang, Ellen Richardson, Oanh Hong, Shawn Cho, Omar Shanta, Timothy Pang,[...]. Cell Rep 2019
12
25

Copy number variations in high and low fertility breeding boars.
Tamas Revay, Anh T Quach, Laurence Maignel, Brian Sullivan, W Allan King. BMC Genomics 2015
17
25

Developmental trajectories of neuroanatomical alterations associated with the 16p11.2 Copy Number Variations.
Alonso Cárdenas-de-la-Parra, Sandra Martin-Brevet, Clara Moreau, Borja Rodriguez-Herreros, Vladimir S Fonov, Anne M Maillard, Nicole R Zürcher, Nouchine Hadjikhani, Jacques S Beckmann, Alexandre Reymond,[...]. Neuroimage 2019
5
25

Copy number variations of MTHFSD gene across pig breeds and its association with litter size traits in Chinese indigenous Xiang pig.
Xue-Qin Ran, Hua Pan, Shi-Hui Huang, Chang Liu, Xi Niu, Sheng Li, Jia-Fu Wang. J Anim Physiol Anim Nutr (Berl) 2018
9
25

Intronic CNVs and gene expression variation in human populations.
Maria Rigau, David Juan, Alfonso Valencia, Daniel Rico. PLoS Genet 2019
23
25

Comparative analysis of ovarian transcriptomes between prolific and non-prolific goat breeds via high-throughput sequencing.
X-D Zi, J-Y Lu, H Zhou, L Ma, W Xia, X-R Xiong, D-L Lan, X-H Wu. Reprod Domest Anim 2018
5
25

Gene copy number variation analysis reveals dosage-insensitive expression of CYP2E1.
R Tremmel, K Klein, S Winter, E Schaeffeler, U M Zanger. Pharmacogenomics J 2016
10
25

Spastic paraplegia type 2 associated with axonal neuropathy and apparent PLP1 position effect.
Jennifer A Lee, Ricardo E Madrid, Karen Sperle, Carolyn M Ritterson, Grace M Hobson, James Garbern, James R Lupski, Ken Inoue. Ann Neurol 2006
66
25

VSTM2A suppresses colorectal cancer and antagonizes Wnt signaling receptor LRP6.
Yujuan Dong, Yanquan Zhang, Wei Kang, Guoping Wang, Huarong Chen, Akira Higashimori, Geicho Nakatsu, Minnie Go, Joanna Hm Tong, Shu Zheng,[...]. Theranostics 2019
16
25

A global analysis of CNVs in swine using whole genome sequence data and association analysis with fatty acid composition and growth traits.
Manuel Revilla, Anna Puig-Oliveras, Anna Castelló, Daniel Crespo-Piazuelo, Ediane Paludo, Ana I Fernández, Maria Ballester, Josep M Folch. PLoS One 2017
20
25

Intron Length Coevolution across Mammalian Genomes.
Peter A Keane, Cathal Seoighe. Mol Biol Evol 2016
10
25

Analysis of the SNP loci around transcription start sites related to goat fecundity trait base on whole genome resequencing.
Rui-Qian Zhang, Fang-Nong Lai, Jun-Jie Wang, Hong-Li Zhai, Yong Zhao, Yu-Jiang Sun, Ling-Jiang Min, Wei Shen. Gene 2018
9
25

Selection signatures in goats reveal copy number variants underlying breed-defining coat color phenotypes.
Jan Henkel, Rashid Saif, Vidhya Jagannathan, Corinne Schmocker, Flurina Zeindler, Erika Bangerter, Ursula Herren, Dimitris Posantzis, Zafer Bulut, Philippe Ammann,[...]. PLoS Genet 2019
12
25


Onsite GTP fuelling via DYNAMO1 drives division of mitochondria and peroxisomes.
Yuuta Imoto, Yuichi Abe, Masanori Honsho, Kanji Okumoto, Mio Ohnuma, Haruko Kuroiwa, Tsuneyoshi Kuroiwa, Yukio Fujiki. Nat Commun 2018
14
25

Copy number variation is highly correlated with differential gene expression: a pan-cancer study.
Xin Shao, Ning Lv, Jie Liao, Jinbo Long, Rui Xue, Ni Ai, Donghang Xu, Xiaohui Fan. BMC Med Genet 2019
39
25

E2F1 germline copy number variations and melanoma susceptibility.
Maria Santa Rocca, Clara Benna, Simone Mocellin, Carlo Riccardo Rossi, Aichi Msaki, Andrea Di Nisio, Giuseppe Opocher, Carlo Foresta. J Transl Med 2019
8
25

De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism.
Ash Zawerton, Baojin Yao, J Paige Yeager, Tommaso Pippucci, Abdul Haseeb, Joshua D Smith, Lisa Wischmann, Susanne J Kühl, John C S Dean, Daniela T Pilz,[...]. Am J Hum Genet 2019
15
25

Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSD.
Federica Buonocore, Oliver Clifford-Mobley, Tom F J King, Niccolò Striglioni, Elim Man, Jenifer P Suntharalingham, Ignacio Del Valle, Lin Lin, Carlos F Lagos, Gill Rumsby,[...]. J Endocr Soc 2019
15
25


Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.
Ash Zawerton, Cyril Mignot, Ashley Sigafoos, Patrick R Blackburn, Abdul Haseeb, Kirsty McWalter, Shoji Ichikawa, Caroline Nava, Boris Keren, Perrine Charles,[...]. Genet Med 2020
7
25

Mosaic Brain Aneuploidy in Mental Illnesses: An Association of Low-level Post-zygotic Aneuploidy with Schizophrenia and Comorbid Psychiatric Disorders.
Yuri B Yurov, Svetlana G Vorsanova, Irina A Demidova, Alexei D Kolotii, Ilia V Soloviev, Ivan Y Iourov. Curr Genomics 2018
10
25

Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic features.
Allen N Lamb, Jill A Rosenfeld, Nicholas J Neill, Michael E Talkowski, Ian Blumenthal, Santhosh Girirajan, Debra Keelean-Fuller, Zheng Fan, Jill Pouncey, Cathy Stevens,[...]. Hum Mutat 2012
60
25


Clinical and genetic characterization of a patient with SOX5 haploinsufficiency caused by a de novo balanced reciprocal translocation.
Daisuke Fukushi, Kenichiro Yamada, Kaoru Suzuki, Mie Inaba, Noriko Nomura, Yasuyo Suzuki, Kimiko Katoh, Seiji Mizuno, Nobuaki Wakamatsu. Gene 2018
7
25


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
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.