A citation-based method for searching scientific literature

JianHua Qian, Ngoc Minh Phuong Nguyen, Maryam Rezaei, Bo Huang, YongLing Tao, XiaoFei Zhang, Qi Cheng, HanJin Yang, Ao Asangla, Jacek Majewski, Rima Slim. Eur J Hum Genet 2018
Times Cited: 31







List of co-cited articles
235 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
71
61

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
141
58

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
306
51


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
33
45

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
84
45

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
82
41

A Maternal Functional Module in the Mammalian Oocyte-To-Embryo Transition.
Xukun Lu, Zheng Gao, Dandan Qin, Lei Li. Trends Mol Med 2017
37
38

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
51
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
43
32

Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest.
Jian Mu, Wenjing Wang, Biaobang Chen, Ling Wu, Bin Li, Xiaoyan Mao, Zhihua Zhang, Jing Fu, Yanping Kuang, Xiaoxi Sun,[...]. J Med Genet 2019
31
32

The subcortical maternal complex: multiple functions for one biological structure?
D Bebbere, L Masala, D F Albertini, S Ledda. J Assist Reprod Genet 2016
33
32

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
27
33

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
21
38

Live births in women with recurrent hydatidiform mole and two NLRP7 mutations.
Elie Akoury, Neerja Gupta, Rashmi Bagga, Stephen Brown, Christine Déry, Madhulika Kabra, Radhika Srinivasan, Rima Slim. Reprod Biomed Online 2015
21
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
366
25

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
36
25

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
101
25

Report of four new patients with protein-truncating mutations in C6orf221/KHDC3L and colocalization with NLRP7.
Ramesh Reddy, Elie Akoury, Ngoc Minh Phuong Nguyen, Omar A Abdul-Rahman, Christine Dery, Neerja Gupta, William P Daley, Asangla Ao, Hanene Landolsi, Rosemary Ann Fisher,[...]. Eur J Hum Genet 2013
49
22

NLRPs, the subcortical maternal complex and genomic imprinting.
David Monk, Marta Sanchez-Delgado, Rosemary Fisher. Reproduction 2017
24
29

A KHDC3L mutation resulting in recurrent hydatidiform mole causes genome-wide DNA methylation loss in oocytes and persistent imprinting defects post-fertilisation.
Hannah Demond, Zahra Anvar, Bahia Namavar Jahromi, Angela Sparago, Ankit Verma, Maryam Davari, Luciano Calzari, Silvia Russo, Mojgan Akbarzadeh Jahromi, David Monk,[...]. Genome Med 2019
17
41

Genetics and Epigenetics of Recurrent Hydatidiform Moles: Basic Science and Genetic Counselling.
Ngoc Minh Phuong Nguyen, Rima Slim. Curr Obstet Gynecol Rep 2014
48
19

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
25
24

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
64
19

Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).
Esther Meyer, Derek Lim, Shanaz Pasha, Louise J Tee, Fatimah Rahman, John R W Yates, C Geoffrey Woods, Wolf Reik, Eamonn R Maher. PLoS Genet 2009
155
19

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
51
19

A global disorder of imprinting in the human female germ line.
Hannah Judson, Bruce E Hayward, Eamonn Sheridan, David T Bonthron. Nature 2002
166
19

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
15
40

Genomic imprinting disorders: lessons on how genome, epigenome and environment interact.
David Monk, Deborah J G Mackay, Thomas Eggermann, Eamonn R Maher, Andrea Riccio. Nat Rev Genet 2019
96
19


Peptidylarginine deiminase (PAD) 6 is essential for oocyte cytoskeletal sheet formation and female fertility.
G Esposito, A M Vitale, F P J Leijten, A M Strik, A M C B Koonen-Reemst, P Yurttas, T J A A Robben, S Coonrod, J A Gossen. Mol Cell Endocrinol 2007
85
19

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
10
60

The genetics of recurrent hydatidiform moles in China: correlations between NLRP7 mutations, molar genotypes and reproductive outcomes.
Jianhua Qian, Qi Cheng, Sharlene Murdoch, Chengming Xu, Fan Jin, Wafaa Chebaro, Xiaofei Zhang, Huijuan Gao, Yimin Zhu, Rima Slim,[...]. Mol Hum Reprod 2011
33
16

Genetic and epigenetic analysis of recurrent hydatidiform mole.
Bruce E Hayward, Michel De Vos, Nargese Talati, M Reza Abdollahi, Graham R Taylor, Esther Meyer, Denise Williams, Eamonn R Maher, Faridon Setna, Kausar Nazir,[...]. Hum Mutat 2009
84
16

What a difference an egg makes.
Rosemary A Fisher, Stuart A Lavery, Anna Carby, Shadi Abu-Hayyeh, Rebecca Swingler, Neil J Sebire, Michael J Seckl. Lancet 2011
32
16

A recurrent intragenic genomic duplication, other novel mutations in NLRP7 and imprinting defects in recurrent biparental hydatidiform moles.
Y C Kou, L Shao, H H Peng, R Rosetta, D del Gaudio, A F Wagner, T K Al-Hussaini, I B Van den Veyver. Mol Hum Reprod 2008
94
16

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
52
16


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
103
16


Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57.
Deborah J G Mackay, Jonathan L A Callaway, Sophie M Marks, Helen E White, Carlo L Acerini, Susanne E Boonen, Pinar Dayanikli, Helen V Firth, Judith A Goodship, Andreas P Haemers,[...]. Nat Genet 2008
336
16

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
27
18

Disturbed genomic imprinting and its relevance for human reproduction: causes and clinical consequences.
Miriam Elbracht, Deborah Mackay, Matthias Begemann, Karl Oliver Kagan, Thomas Eggermann. Hum Reprod Update 2020
13
38

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
8
62

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
9
55

Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance.
Maria Vittoria Cubellis, Laura Pignata, Ankit Verma, Angela Sparago, Rosita Del Prete, Maria Monticelli, Luciano Calzari, Vincenzo Antona, Daniela Melis, Romano Tenconi,[...]. Clin Epigenetics 2020
12
41

Maternal control of early mouse development.
Lei Li, Ping Zheng, Jurrien Dean. Development 2010
259
12

Expression analysis of the NLRP gene family suggests a role in human preimplantation development.
Pu Zhang, Morag Dixon, Marco Zucchelli, Fredwell Hambiliki, Lev Levkov, Outi Hovatta, Juha Kere. PLoS One 2008
90
12

Identification of 13 novel NLRP7 mutations in 20 families with recurrent hydatidiform mole; missense mutations cluster in the leucine-rich region.
C M Wang, P H Dixon, S Decordova, M D Hodges, N J Sebire, S Ozalp, M Fallahian, A Sensi, F Ashrafi, V Repiska,[...]. J Med Genet 2009
93
12

The p.L750V mutation in the NLRP7 gene is frequent in Mexican patients with recurrent molar pregnancies and is not associated with recurrent pregnancy loss.
Higinio Estrada, Beatriz Buentello, Juan Carlos Zenteno, Rachel Fiszman, Mónica Aguinaga. Prenat Diagn 2013
18
22


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.