A citation-based method for searching scientific literature

Xiaojun Ren, Nan Yang, Nan Wu, Ximing Xu, Weisheng Chen, Ling Zhang, Yingping Li, Ren-Qian Du, Shuangshuang Dong, Sen Zhao, Shuxia Chen, Li-Ping Jiang, Lianlei Wang, Jianguo Zhang, Zhihong Wu, Li Jin, Guixing Qiu, James R Lupski, Jiangang Shi, Feng Zhang, Pengfei Liu. J Med Genet 2020
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


TBX6 null variants and a common hypomorphic allele in congenital scoliosis.
N Wu, X Ming, J Xiao, Z Wu, X Chen, M Shinawi, Y Shen, G Yu, J Liu, H Xie,[...]. N Engl J Med 2015
145
62

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Priya Krithivasan, Adele Mitrotti, David A Fasel, Ekaterina Batourina, Matthew G Sampson,[...]. Nat Genet 2019
46
50

Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesia.
Patrick Lorès, Charles Coutton, Elma El Khouri, Laurence Stouvenel, Maëlle Givelet, Lucie Thomas, Baptiste Rode, Alain Schmitt, Bruno Louis, Zeinab Sakheli,[...]. Hum Mol Genet 2018
48
25

IFT25, an intraflagellar transporter protein dispensable for ciliogenesis in somatic cells, is essential for sperm flagella formation.
Hong Liu, Wei Li, Yong Zhang, Zhengang Zhang, Xuejun Shang, Ling Zhang, Shiyang Zhang, Yanwei Li, Andres V Somoza, Brandon Delpi,[...]. Biol Reprod 2017
30
25

Intraflagellar transporter protein 140 (IFT140), a component of IFT-A complex, is essential for male fertility and spermiogenesis in mice.
Yong Zhang, Hong Liu, Wei Li, Zhengang Zhang, Shiyang Zhang, Maria E Teves, Courtney Stevens, James A Foster, Gregory E Campbell, Jolene J Windle,[...]. Cytoskeleton (Hoboken) 2018
20
25

Mutations in CFAP43 and CFAP44 cause male infertility and flagellum defects in Trypanosoma and human.
Charles Coutton, Alexandra S Vargas, Amir Amiri-Yekta, Zine-Eddine Kherraf, Selima Fourati Ben Mustapha, Pauline Le Tanno, Clémentine Wambergue-Legrand, Thomas Karaouzène, Guillaume Martinez, Serge Crouzy,[...]. Nat Commun 2018
82
25

Intraflagellar transport protein IFT20 is essential for male fertility and spermiogenesis in mice.
Zhengang Zhang, Wei Li, Yong Zhang, Ling Zhang, Maria E Teves, Hong Liu, Jerome F Strauss, Gregory J Pazour, James A Foster, Rex A Hess,[...]. Mol Biol Cell 2016
39
25

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse.
Frederick N Dong, Amir Amiri-Yekta, Guillaume Martinez, Antoine Saut, Julie Tek, Laurence Stouvenel, Patrick Lorès, Thomas Karaouzène, Nicolas Thierry-Mieg, Véronique Satre,[...]. Am J Hum Genet 2018
60
25

Loss of SPEF2 function in mice results in spermatogenesis defects and primary ciliary dyskinesia.
Anu Sironen, Noora Kotaja, Howard Mulhern, Todd A Wyatt, Joseph H Sisson, Jacqueline A Pavlik, Mari Miiluniemi, Mark D Fleming, Lance Lee. Biol Reprod 2011
74
25

1001 model organisms to study cilia and flagella.
Laetitia Vincensini, Thierry Blisnick, Philippe Bastin. Biol Cell 2011
77
25

Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella.
Xiaojin He, Weiyu Li, Huan Wu, Mingrong Lv, Wangjie Liu, Chunyu Liu, Fuxi Zhu, Caihua Li, Youyan Fang, Chenyu Yang,[...]. J Med Genet 2019
33
25

Intraflagellar transport is essential for mammalian spermiogenesis but is absent in mature sperm.
Jovenal T San Agustin, Gregory J Pazour, George B Witman. Mol Biol Cell 2015
53
25

Mutations in TTC29, Encoding an Evolutionarily Conserved Axonemal Protein, Result in Asthenozoospermia and Male Infertility.
Patrick Lorès, Denis Dacheux, Zine-Eddine Kherraf, Jean-Fabrice Nsota Mbango, Charles Coutton, Laurence Stouvenel, Come Ialy-Radio, Amir Amiri-Yekta, Marjorie Whitfield, Alain Schmitt,[...]. Am J Hum Genet 2019
12
25

Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF).
Wensheng Liu, Yanwei Sha, Yang Li, Libin Mei, Shaobin Lin, Xianjing Huang, Jinhua Lu, Lu Ding, Shuangbo Kong, Zhongxian Lu. J Med Genet 2019
31
25

In-depth proteomic analysis of the human sperm reveals complex protein compositions.
Gaigai Wang, Yueshuai Guo, Tao Zhou, Xiaodan Shi, Jun Yu, Ye Yang, Yibo Wu, Jing Wang, Mingxi Liu, Xin Chen,[...]. J Proteomics 2013
118
25

Intraflagellar transporter protein (IFT27), an IFT25 binding partner, is essential for male fertility and spermiogenesis in mice.
Yong Zhang, Hong Liu, Wei Li, Zhengang Zhang, Xuejun Shang, David Zhang, Yuhong Li, Shiyang Zhang, Junpin Liu, Rex A Hess,[...]. Dev Biol 2017
31
25

World Health Organization reference values for human semen characteristics.
Trevor G Cooper, Elizabeth Noonan, Sigrid von Eckardstein, Jacques Auger, H W Gordon Baker, Hermann M Behre, Trine B Haugen, Thinus Kruger, Christina Wang, Michael T Mbizvo,[...]. Hum Reprod Update 2010
25

Another look at human sperm morphology.
J Auger, P Jouannet, F Eustache. Hum Reprod 2016
59
25

Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility.
Chunyu Liu, Mingrong Lv, Xiaojin He, Yong Zhu, Amir Amiri-Yekta, Weiyu Li, Huan Wu, Zine-Eddine Kherraf, Wangjie Liu, Jingjing Zhang,[...]. J Med Genet 2020
29
25

Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice.
Wangjie Liu, Xiaojin He, Shenmin Yang, Raoudha Zouari, Jiaxiong Wang, Huan Wu, Zine-Eddine Kherraf, Chunyu Liu, Charles Coutton, Rui Zhao,[...]. Am J Hum Genet 2019
41
25

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
792
25

Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway.
Justyna A Karolak, Marie Vincent, Gail Deutsch, Tomasz Gambin, Benjamin Cogné, Olivier Pichon, Francesco Vetrini, Heather C Mefford, Jennifer N Dines, Katie Golden-Grant,[...]. Am J Hum Genet 2019
36
25

TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice.
Nan Yang, Nan Wu, Ling Zhang, Yanxue Zhao, Jiaqi Liu, Xiangyu Liang, Xiaojun Ren, Weiyu Li, Weisheng Chen, Shuangshuang Dong,[...]. Hum Mol Genet 2019
26
25

Compound inheritance of a low-frequency regulatory SNP and a rare null mutation in exon-junction complex subunit RBM8A causes TAR syndrome.
Cornelis A Albers, Dirk S Paul, Harald Schulze, Kathleen Freson, Jonathan C Stephens, Peter A Smethurst, Jennifer D Jolley, Ana Cvejic, Myrto Kostadima, Paul Bertone,[...]. Nat Genet 2012
251
25


TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model.
Jiaqi Liu, Nan Wu, Nan Yang, Kazuki Takeda, Weisheng Chen, Weiyu Li, Renqian Du, Sen Liu, Yangzhong Zhou, Ling Zhang,[...]. Genet Med 2019
24
25

Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
Marwan Shinawi, Pengfei Liu, Sung-Hae L Kang, Joseph Shen, John W Belmont, Daryl A Scott, Frank J Probst, William J Craigen, Brett H Graham, Amber Pursley,[...]. J Med Genet 2010
317
25

Identification of novel candidate disease genes from de novo exonic copy number variants.
Tomasz Gambin, Bo Yuan, Weimin Bi, Pengfei Liu, Jill A Rosenfeld, Zeynep Coban-Akdemir, Amber N Pursley, Sandesh C S Nagamani, Ronit Marom, Sailaja Golla,[...]. Genome Med 2017
35
25

Reanalysis of Clinical Exome Sequencing Data.
Pengfei Liu, Linyan Meng, Elizabeth A Normand, Fan Xia, Xiaofei Song, Andrew Ghazi, Jill Rosenfeld, Pilar L Magoulas, Alicia Braxton, Patricia Ward,[...]. N Engl J Med 2019
59
25

Copy number variant and runs of homozygosity detection by microarrays enabled more precise molecular diagnoses in 11,020 clinical exome cases.
Avinash V Dharmadhikari, Rajarshi Ghosh, Bo Yuan, Pengfei Liu, Hongzheng Dai, Sami Al Masri, Jennifer Scull, Jennifer E Posey, Allen H Jiang, Weimin He,[...]. Genome Med 2019
10
25

Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation.
Jennifer E Posey, Tamar Harel, Pengfei Liu, Jill A Rosenfeld, Regis A James, Zeynep H Coban Akdemir, Magdalena Walkiewicz, Weimin Bi, Rui Xiao, Yan Ding,[...]. N Engl J Med 2017
316
25

Novel Mutations in CFAP44 and CFAP43 Cause Multiple Morphological Abnormalities of the Sperm Flagella (MMAF).
Yan-Wei Sha, Xiong Wang, Xiaohui Xu, Zhi-Ying Su, Yuanqing Cui, Li-Bin Mei, Xian-Jing Huang, Jie Chen, Xue-Mei He, Zhi-Yong Ji,[...]. Reprod Sci 2019
21
12

A microtubule-dynein tethering complex regulates the axonemal inner dynein f (I1).
Tomohiro Kubo, Yuqing Hou, Deborah A Cochran, George B Witman, Toshiyuki Oda. Mol Biol Cell 2018
25
12

Mutations in DNAH1, which encodes an inner arm heavy chain dynein, lead to male infertility from multiple morphological abnormalities of the sperm flagella.
Mariem Ben Khelifa, Charles Coutton, Raoudha Zouari, Thomas Karaouzène, John Rendu, Marie Bidart, Sandra Yassine, Virginie Pierre, Julie Delaroche, Sylviane Hennebicq,[...]. Am J Hum Genet 2014
168
12

[Morphological defects of sperm flagellum implicated in human male infertility].
Denise Escalier, Aminata Touré. Med Sci (Paris) 2012
6
16


Loss of Calmodulin- and Radial-Spoke-Associated Complex Protein CFAP251 Leads to Immotile Spermatozoa Lacking Mitochondria and Infertility in Men.
Yasmina Auguste, Valérie Delague, Jean-Pierre Desvignes, Guy Longepied, Audrey Gnisci, Pierre Besnier, Nicolas Levy, Christophe Beroud, André Megarbane, Catherine Metzler-Guillemain,[...]. Am J Hum Genet 2018
36
12


Primary Ciliary Dyskinesia.
Michael R Knowles, Maimoona Zariwala, Margaret Leigh. Clin Chest Med 2016
74
12

Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice.
Weiyu Li, Huan Wu, Fuping Li, Shixiong Tian, Zine-Eddine Kherraf, Jintao Zhang, Xiaoqing Ni, Mingrong Lv, Chunyu Liu, Qing Tan,[...]. J Med Genet 2020
17
12

The CSC proteins FAP61 and FAP251 build the basal substructures of radial spoke 3 in cilia.
Paulina Urbanska, Kangkang Song, Ewa Joachimiak, Lucja Krzemien-Ojak, Piotr Koprowski, Todd Hennessey, Maria Jerka-Dziadosz, Hanna Fabczak, Jacek Gaertig, Daniela Nicastro,[...]. Mol Biol Cell 2015
32
12

Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders.
Justin O Szot, Carla Campagnolo, Ye Cao, Kavitha R Iyer, Hartmut Cuny, Thomas Drysdale, Josue A Flores-Daboub, Weimin Bi, Lauren Westerfield, Pengfei Liu,[...]. Am J Hum Genet 2020
8
12

Gene trap mutation of murine outer dense fiber protein-2 gene can result in sperm tail abnormalities in mice with high percentage chimaerism.
Heide Tarnasky, Min Cheng, Young Ou, Jacob C Thundathil, Richard Oko, Frans A van der Hoorn. BMC Dev Biol 2010
41
12

Variation in Cilia Protein Genes and Progression of Lung Disease in Cystic Fibrosis.
Elizabeth Blue, Tin L Louie, Jessica X Chong, Scott J Hebbring, Kathleen C Barnes, Nicholas M Rafaels, Michael R Knowles, Ronald L Gibson, Michael J Bamshad, Mary J Emond. Ann Am Thorac Soc 2018
12
12

Molecular chaperones, cochaperones, and ubiquitination/deubiquitination system: involvement in the production of high quality spermatozoa.
Rosaria Meccariello, Rosanna Chianese, Vincenza Ciaramella, Silvia Fasano, Riccardo Pierantoni. Biomed Res Int 2014
16
12

Networking with AKAPs: context-dependent regulation of anchored enzymes.
Emily J Welch, Brian W Jones, John D Scott. Mol Interv 2010
123
12


DNAH6 is a novel candidate gene associated with sperm head anomaly.
L Li, Y-W Sha, X Xu, L-B Mei, P-P Qiu, Z-Y Ji, S-B Lin, Z-Y Su, C Wang, C Yin,[...]. Andrologia 2018
16
12

DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia.
You Li, Hisato Yagi, Ezenwa Obi Onuoha, Rama Rao Damerla, Richard Francis, Yoshiyuki Furutani, Muhammad Tariq, Stephen M King, Gregory Hendricks, Cheng Cui,[...]. PLoS Genet 2016
48
12

Targeted disruption of the Akap4 gene causes defects in sperm flagellum and motility.
Kiyoshi Miki, William D Willis, Paula R Brown, Eugenia H Goulding, Kerry D Fulcher, Edward M Eddy. Dev Biol 2002
251
12


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.