A citation-based method for searching scientific literature

Jian Mu, Wenjing Wang, Biaobang Chen, Ling Wu, Bin Li, Xiaoyan Mao, Zhihua Zhang, Jing Fu, Yanping Kuang, Xiaoxi Sun, Qiaoli Li, Li Jin, Lin He, Qing Sang, Lei Wang. J Med Genet 2019
Times Cited: 42







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



Times Cited
  Times     Co-cited
Similarity


Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest.
Yao Xu, Yingli Shi, Jing Fu, Min Yu, Ruizhi Feng, Qing Sang, Bo Liang, Biaobang Chen, Ronggui Qu, Bin Li,[...]. Am J Hum Genet 2016
91
80

TLE6 mutation causes the earliest known human embryonic lethality.
Anas M Alazami, Salma M Awad, Serdar Coskun, Saad Al-Hassan, Hadia Hijazi, Firdous M Abdulwahab, Coralie Poizat, Fowzan S Alkuraya. Genome Biol 2015
99
78

Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest.
Xueqian Wang, Di Song, Dmytro Mykytenko, Yanping Kuang, Qifeng Lv, Bin Li, Biaobang Chen, Xiaoyan Mao, Yao Xu, Valery Zukin,[...]. Reprod Biomed Online 2018
40
57

Mutations in TUBB8 and Human Oocyte Meiotic Arrest.
Ruizhi Feng, Qing Sang, Yanping Kuang, Xiaoxi Sun, Zheng Yan, Shaozhen Zhang, Juanzi Shi, Guoling Tian, Anna Luchniak, Yusuke Fukuda,[...]. N Engl J Med 2016
118
47

Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest.
Biaobang Chen, Zhihua Zhang, Xiaoxi Sun, Yanping Kuang, Xiaoyan Mao, Xueqian Wang, Zheng Yan, Bin Li, Yao Xu, Min Yu,[...]. Am J Hum Genet 2017
60
42


A Maternal Functional Module in the Mammalian Oocyte-To-Embryo Transition.
Xukun Lu, Zheng Gao, Dandan Qin, Lei Li. Trends Mol Med 2017
45
38

Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.
Qing Sang, Bin Li, Yanping Kuang, Xueqian Wang, Zhihua Zhang, Biaobang Chen, Ling Wu, Qifeng Lyu, Yonglun Fu, Zheng Yan,[...]. Am J Hum Genet 2018
74
38

Mater, a maternal effect gene required for early embryonic development in mice.
Z B Tong, L Gold, K E Pfeifer, H Dorward, E Lee, C A Bondy, J Dean, L M Nelson. Nat Genet 2000
375
38

Identification of a human subcortical maternal complex.
Kai Zhu, Liying Yan, Xiaoxin Zhang, Xukun Lu, Tianren Wang, Jie Yan, Xinqi Liu, Jie Qiao, Lei Li. Mol Hum Reprod 2015
49
35

Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte.
David A Parry, Clare V Logan, Bruce E Hayward, Michael Shires, Hanène Landolsi, Christine Diggle, Ian Carr, Cécile Rittore, Isabelle Touitou, Laurent Philibert,[...]. Am J Hum Genet 2011
148
33

Mutations in NLRP5 are associated with reproductive wastage and multilocus imprinting disorders in humans.
Louise E Docherty, Faisal I Rezwan, Rebecca L Poole, Claire L S Turner, Emma Kivuva, Eamonn R Maher, Sarah F Smithson, Julian P Hamilton-Shield, Michal Patalan, Maria Gizewska,[...]. Nat Commun 2015
87
33

The subcortical maternal complex controls symmetric division of mouse zygotes by regulating F-actin dynamics.
Xing-Jiang Yu, Zhaohong Yi, Zheng Gao, Dandan Qin, Yanhua Zhai, Xue Chen, Yingchun Ou-Yang, Zhen-Bo Wang, Ping Zheng, Min-Sheng Zhu,[...]. Nat Commun 2014
58
33

Biallelic PADI6 variants linking infertility, miscarriages, and hydatidiform moles.
JianHua Qian, Ngoc Minh Phuong Nguyen, Maryam Rezaei, Bo Huang, YongLing Tao, XiaoFei Zhang, Qi Cheng, HanJin Yang, Ao Asangla, Jacek Majewski,[...]. Eur J Hum Genet 2018
37
35

Maternally expressed NLRP2 links the subcortical maternal complex (SCMC) to fertility, embryogenesis and epigenetic reprogramming.
Sangeetha Mahadevan, Varsha Sathappan, Budi Utama, Isabel Lorenzo, Khalied Kaskar, Ignatia B Van den Veyver. Sci Rep 2017
41
31

Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring.
Matthias Begemann, Faisal I Rezwan, Jasmin Beygo, Louise E Docherty, Julia Kolarova, Christopher Schroeder, Karin Buiting, Kamal Chokkalingam, Franziska Degenhardt, Emma L Wakeling,[...]. J Med Genet 2018
59
30

Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos.
Ruizhi Feng, Zheng Yan, Bin Li, Min Yu, Qing Sang, Guoling Tian, Yao Xu, Biaobang Chen, Ronggui Qu, Zhaogui Sun,[...]. J Med Genet 2016
60
28

Female Infertility Caused by Mutations in the Oocyte-Specific Translational Repressor PATL2.
Sateesh Maddirevula, Serdar Coskun, Saad Alhassan, Atif Elnour, Hessa S Alsaif, Niema Ibrahim, Firdous Abdulwahab, Stefan T Arold, Fowzan S Alkuraya. Am J Hum Genet 2017
33
36

Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
Sharlene Murdoch, Ugljesa Djuric, Batool Mazhar, Muheiddine Seoud, Rabia Khan, Rork Kuick, Rashmi Bagga, Renate Kircheisen, Asangla Ao, Bhawna Ratti,[...]. Nat Genet 2006
313
26

A novel homozygous variant in NLRP5 is associate with human early embryonic arrest in a consanguineous Chinese family.
Yao Xu, Ying Qian, Yu Liu, Qiaofeng Wang, Rongxiang Wang, Yiwen Zhou, Caixia Zhang, Zhi Pang, Hongjuan Ye, Songguo Xue,[...]. Clin Genet 2020
14
78

Role for PADI6 and the cytoplasmic lattices in ribosomal storage in oocytes and translational control in the early mouse embryo.
Piraye Yurttas, Alejandra M Vitale, Robert J Fitzhenry, Leona Cohen-Gould, Wenzhu Wu, Jan A Gossen, Scott A Coonrod. Development 2008
111
23

Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility.
Ling Wu, Hua Chen, Da Li, Di Song, Biaobang Chen, Zheng Yan, Qifeng Lyu, Lei Wang, Yanping Kuang, Bin Li,[...]. J Hum Genet 2019
18
55

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility.
Biaobang Chen, Wenjing Wang, Xiandong Peng, Huafeng Jiang, Shaozhen Zhang, Da Li, Bin Li, Jing Fu, Yanping Kuang, Xiaoxi Sun,[...]. Eur J Hum Genet 2019
33
30

The subcortical maternal complex: multiple functions for one biological structure?
D Bebbere, L Masala, D F Albertini, S Ledda. J Assist Reprod Genet 2016
38
26

Expanding the genetic and phenotypic spectrum of female infertility caused by TLE6 mutations.
Jing Lin, Hua Xu, Biaobang Chen, Wenjing Wang, Lei Wang, Xiaoxi Sun, Qing Sang. J Assist Reprod Genet 2020
13
76

Bi-allelic Missense Pathogenic Variants in TRIP13 Cause Female Infertility Characterized by Oocyte Maturation Arrest.
Zhihua Zhang, Bin Li, Jing Fu, Rong Li, Feiyang Diao, Caihong Li, Biaobang Chen, Jing Du, Zhou Zhou, Jian Mu,[...]. Am J Hum Genet 2020
22
45

Novel mutations in PATL2 cause female infertility with oocyte germinal vesicle arrest.
Lingli Huang, Xianhong Tong, Fengsong Wang, Lihua Luo, Rentao Jin, Yingyun Fu, Guixiang Zhou, Daojing Li, Gaojie Song, Yusheng Liu,[...]. Hum Reprod 2018
22
40

A genomics approach to females with infertility and recurrent pregnancy loss.
Sateesh Maddirevula, Khalid Awartani, Serdar Coskun, Latifa F AlNaim, Niema Ibrahim, Firdous Abdulwahab, Mais Hashem, Saad Alhassan, Fowzan S Alkuraya. Hum Genet 2020
20
45

New biallelic mutations in PADI6 cause recurrent preimplantation embryonic arrest characterized by direct cleavage.
Wei Zheng, Longbin Chen, Jing Dai, Can Dai, Jing Guo, Changfu Lu, Fei Gong, Guangxiu Lu, Ge Lin. J Assist Reprod Genet 2020
17
52

Causative Mutations and Mechanism of Androgenetic Hydatidiform Moles.
Ngoc Minh Phuong Nguyen, Zhao-Jia Ge, Ramesh Reddy, Somayyeh Fahiminiya, Philippe Sauthier, Rashmi Bagga, Feride Iffet Sahin, Sangeetha Mahadevan, Matthew Osmond, Magali Breguet,[...]. Am J Hum Genet 2018
31
25



The human knockout phenotype of PADI6 is female sterility caused by cleavage failure of their fertilized eggs.
S Maddirevula, S Coskun, K Awartani, H Alsaif, F M Abdulwahab, F S Alkuraya. Clin Genet 2017
20
40


Mutant ZP1 in familial infertility.
Hua-Lin Huang, Chao Lv, Ying-Chun Zhao, Wen Li, Xue-Mei He, Ping Li, Ai-Guo Sha, Xiao Tian, Christopher J Papasian, Hong-Wen Deng,[...]. N Engl J Med 2014
64
16

Maternal control of early mouse development.
Lei Li, Ping Zheng, Jurrien Dean. Development 2010
269
16

PATL2 is a key actor of oocyte maturation whose invalidation causes infertility in women and mice.
Marie Christou-Kent, Zine-Eddine Kherraf, Amir Amiri-Yekta, Emilie Le Blévec, Thomas Karaouzène, Béatrice Conne, Jessica Escoffier, Said Assou, Audrey Guttin, Emeline Lambert,[...]. EMBO Mol Med 2018
27
25

Homozygous Mutations in BTG4 Cause Zygotic Cleavage Failure and Female Infertility.
Wei Zheng, Zhou Zhou, Qianqian Sha, Xiangli Niu, Xiaoxi Sun, Juanzi Shi, Lei Zhao, Shuoping Zhang, Jing Dai, Sufen Cai,[...]. Am J Hum Genet 2020
16
43

Maternal heterozygous NLRP7 variant results in recurrent reproductive failure and imprinting disturbances in the offspring.
Lukas Soellner, Matthias Begemann, Franziska Degenhardt, Annegret Geipel, Thomas Eggermann, Elisabeth Mangold. Eur J Hum Genet 2017
26
23

A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility.
Tailai Chen, Yuehong Bian, Xiaoman Liu, Shigang Zhao, Keliang Wu, Lei Yan, Mei Li, Zhenglin Yang, Hongbin Liu, Han Zhao,[...]. Am J Hum Genet 2017
53
14

A pannexin 1 channelopathy causes human oocyte death.
Qing Sang, Zhihua Zhang, Juanzi Shi, Xiaoxi Sun, Bin Li, Zheng Yan, Songguo Xue, Ai Ai, Qifeng Lyu, Wei Li,[...]. Sci Transl Med 2019
38
15

NLRPs, the subcortical maternal complex and genomic imprinting.
David Monk, Marta Sanchez-Delgado, Rosemary Fisher. Reproduction 2017
30
20

Maternal-effect gene Ces5/Ooep/Moep19/Floped is essential for oocyte cytoplasmic lattice formation and embryonic development at the maternal-zygotic stage transition.
Fumi Tashiro, Masami Kanai-Azuma, Satsuki Miyazaki, Masahiro Kato, Tomofumi Tanaka, Shuichi Toyoda, Eiji Yamato, Hayato Kawakami, Tatsushi Miyazaki, Jun-Ichi Miyazaki. Genes Cells 2010
46
14

Genetics of human female infertility†.
Svetlana A Yatsenko, Aleksandar Rajkovic. Biol Reprod 2019
41
14

Mutation analysis of the TUBB8 gene in nine infertile women with oocyte maturation arrest.
Lingli Huang, Xianhong Tong, Lihua Luo, Shengxia Zheng, Rentao Jin, Yingyun Fu, Guixiang Zhou, Daojing Li, Yusheng Liu. Reprod Biomed Online 2017
34
17

Dynamics and clinical relevance of maternal mRNA clearance during the oocyte-to-embryo transition in humans.
Qian-Qian Sha, Wei Zheng, Yun-Wen Wu, Sen Li, Lei Guo, Shuoping Zhang, Ge Lin, Xiang-Hong Ou, Heng-Yu Fan. Nat Commun 2020
23
26

Mutant cohesin in premature ovarian failure.
Sandrine Caburet, Valerie A Arboleda, Elena Llano, Paul A Overbeek, Jose Luis Barbero, Kazuhiro Oka, Wilbur Harrison, Daniel Vaiman, Ziva Ben-Neriah, Ignacio García-Tuñón,[...]. N Engl J Med 2014
176
11

The genetics of recurrent hydatidiform moles: new insights and lessons from a comprehensive analysis of 113 patients.
Ngoc Minh Phuong Nguyen, Yassemine Khawajkie, Nawel Mechtouf, Maryam Rezaei, Magali Breguet, Elvira Kurvinen, Sujatha Jagadeesh, Asli Ece Solmaz, Monica Aguinaga, Reda Hemida,[...]. Mod Pathol 2018
32
15

Human oocyte developmental potential is predicted by mechanical properties within hours after fertilization.
Livia Z Yanez, Jinnuo Han, Barry B Behr, Renee A Reijo Pera, David B Camarillo. Nat Commun 2016
81
11

New biallelic mutations in WEE2: expanding the spectrum of mutations that cause fertilization failure or poor fertilization.
Jing Dai, Wei Zheng, Can Dai, Jing Guo, Changfu Lu, Fei Gong, Yan Li, Qinwei Zhou, Guangxiu Lu, Ge Lin. Fertil Steril 2019
18
27


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.