A citation-based method for searching scientific literature

Sintia Kolbjer, Daniel A Martin, Maria Pettersson, Maria Dahlin, Britt-Marie Anderlid. Eur J Paediatr Neurol 2021
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly.
Nataliya Di Donato, Andrew E Timms, Kimberly A Aldinger, Ghayda M Mirzaa, James T Bennett, Sarah Collins, Carissa Olds, Davide Mei, Sara Chiari, Gemma Carvill,[...]. Genet Med 2018
52
33

Neuropathology of genetically defined malformations of cortical development-A systematic literature review.
Stefanie Brock, Filip Cools, Anna C Jansen. Neuropathol Appl Neurobiol 2021
6
50

Lissencephaly: Expanded imaging and clinical classification.
Nataliya Di Donato, Sara Chiari, Ghayda M Mirzaa, Kimberly Aldinger, Elena Parrini, Carissa Olds, A James Barkovich, Renzo Guerrini, William B Dobyns. Am J Med Genet A 2017
51
22

Definitions and classification of malformations of cortical development: practical guidelines.
Mariasavina Severino, Ana Filipa Geraldo, Norbert Utz, Domenico Tortora, Ivana Pogledic, Wlodzimierz Klonowski, Fabio Triulzi, Filippo Arrigoni, Kshitij Mankad, Richard J Leventer,[...]. Brain 2020
40
22

Genotypically defined lissencephalies show distinct pathologies.
Mark S Forman, Waney Squier, William B Dobyns, Jeffrey A Golden. J Neuropathol Exp Neurol 2005
78
22

A developmental and genetic classification for midbrain-hindbrain malformations.
A James Barkovich, Kathleen J Millen, William B Dobyns. Brain 2009
155
22


Epilepsy in Tubulinopathy: Personal Series and Literature Review.
Romina Romaniello, Claudio Zucca, Filippo Arrigoni, Paolo Bonanni, Elena Panzeri, Maria T Bassi, Renato Borgatti. Cells 2019
12
22

Recognizable cerebellar dysplasia associated with mutations in multiple tubulin genes.
Renske Oegema, Thomas D Cushion, Ian G Phelps, Seo-Kyung Chung, Jennifer C Dempsey, Sarah Collins, Jonathan G L Mullins, Tracy Dudding, Harinder Gill, Andrew J Green,[...]. Hum Mol Genet 2015
53
22

The clinical-phenotype continuum in DYNC1H1-related disorders-genomic profiling and proposal for a novel classification.
Lena-Luise Becker, Hormos Salimi Dafsari, Jens Schallner, Dalia Abdin, Michael Seifert, Florence Petit, Thomas Smol, Levinus Bok, Lance Rodan, Ingrid Krapels,[...]. J Hum Genet 2020
10
22

The wide spectrum of tubulinopathies: what are the key features for the diagnosis?
Nadia Bahi-Buisson, Karine Poirier, Franck Fourniol, Yoann Saillour, Stéphanie Valence, Nicolas Lebrun, Marie Hully, Catherine Fallet Bianco, Nathalie Boddaert, Caroline Elie,[...]. Brain 2014
161
22

Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly.
Catherine Fallet-Bianco, Annie Laquerrière, Karine Poirier, Ferechte Razavi, Fabien Guimiot, Patricia Dias, Laurence Loeuillet, Karine Lascelles, Cherif Beldjord, Nathalie Carion,[...]. Acta Neuropathol Commun 2014
66
22

Malformations of Cortical Development: From Postnatal to Fetal Imaging.
Tally Lerman-Sagie, Zvi Leibovitz. Can J Neurol Sci 2016
17
22

Malformations of cortical development and epilepsy.
A James Barkovich, William B Dobyns, Renzo Guerrini. Cold Spring Harb Perspect Med 2015
60
22


Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly.
Karine Poirier, Nicolas Lebrun, Loic Broix, Guoling Tian, Yoann Saillour, Cécile Boscheron, Elena Parrini, Stephanie Valence, Benjamin Saint Pierre, Madison Oger,[...]. Nat Genet 2013
262
22

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
22

Lissencephaly: Update on diagnostics and clinical management.
Matti Koenig, William B Dobyns, Nataliya Di Donato. Eur J Paediatr Neurol 2021
3
66

The utility of exome sequencing for genetic diagnosis in a familial microcephaly epilepsy syndrome.
Laura M McDonell, Jodi Warman Chardon, Jeremy Schwartzentruber, Denise Foster, Chandree L Beaulieu, Jacek Majewski, Dennis E Bulman, Kym M Boycott. BMC Neurol 2014
9
11

Phosphorylation of SCG10/stathmin-2 determines multipolar stage exit and neuronal migration rate.
Nina Westerlund, Justyna Zdrojewska, Artur Padzik, Emilia Komulainen, Benny Björkblom, Emmy Rannikko, Tanya Tararuk, Cristina Garcia-Frigola, Jouko Sandholm, Laurent Nguyen,[...]. Nat Neurosci 2011
86
11

c-Jun N-terminal kinase 2 suppresses pancreatic cancer growth and invasion and is opposed by c-Jun N-terminal kinase 1.
Xiaodong Tian, Benno Traub, Jingwei Shi, Nadine Huber, Stefan Schreiner, Guowei Chen, Shaoxia Zhou, Doris Henne-Bruns, Uwe Knippschild, Marko Kornmann. Cancer Gene Ther 2022
4
25

Pathogenic huntingtin inhibits fast axonal transport by activating JNK3 and phosphorylating kinesin.
Gerardo A Morfini, Yi-Mei You, Sarah L Pollema, Agnieszka Kaminska, Katherine Liu, Katsuji Yoshioka, Benny Björkblom, Eleanor T Coffey, Carolina Bagnato, David Han,[...]. Nat Neurosci 2009
168
11

The JNK Signaling Pathway in Inflammatory Skin Disorders and Cancer.
Manel B Hammouda, Amy E Ford, Yuan Liu, Jennifer Y Zhang. Cells 2020
47
11

mGluR3 promotes proliferation of human embryonic cortical neural progenitor cells by activating ERK1/2 and JNK2 signaling pathway in vitro.
J Guo, X Zhou, Y Chen, M Bai, X Yang, K Zhao, W Hao, W Wei, Y Zhang. Cell Mol Biol (Noisy-le-grand) 2014
9
11

Docking interactions of the JNK scaffold protein WDR62.
Ksenya Cohen-Katsenelson, Tanya Wasserman, Samer Khateb, Alan J Whitmarsh, Ami Aronheim. Biochem J 2011
29
11


JNK supports survival in melanoma cells by controlling cell cycle arrest and apoptosis.
Vasileia-Ismini Alexaki, Delphine Javelaud, Alain Mauviel. Pigment Cell Melanoma Res 2008
48
11

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.
Timothy W Yu, Ganeshwaran H Mochida, David J Tischfield, Sema K Sgaier, Laura Flores-Sarnat, Consolato M Sergi, Meral Topçu, Marie T McDonald, Brenda J Barry, Jillian M Felie,[...]. Nat Genet 2010
205
11

The c-Jun N-terminal kinase JNK functions upstream of Aurora B to promote entry into mitosis.
Kutluk Oktay, Erkan Buyuk, Ozgur Oktem, Maja Oktay, Filippo G Giancotti. Cell Cycle 2008
42
11

WDR62 is involved in spindle assembly by interacting with CEP170 in spermatogenesis.
Yan Qin, Yang Zhou, Zhiming Shen, Binyang Xu, Min Chen, Yaqiong Li, Min Chen, Axel Behrens, Jingjing Zhou, Xin Qi,[...]. Development 2019
9
11

JNK/AP1 Pathway Regulates MYC Expression and BCR Signaling through Ig Enhancers in Burkitt Lymphoma Cells.
Xiaoling Ding, Xiaoying Wang, Xueting Zhu, Jie Zhang, Yiqing Zhu, Xiaoyi Shao, Xiaorong Zhou. J Cancer 2020
5
20

Increased levels of cerebrospinal fluid JNK3 associated with amyloid pathology: links to cognitive decline.
Sarah Gourmaud, Claire Paquet, Julien Dumurgier, Clarisse Pace, Constantin Bouras, Françoise Gray, Jean-Louis Laplanche, Eliane F Meurs, François Mouton-Liger, Jacques Hugon. J Psychiatry Neurosci 2015
56
11

A genetic mosaic screen identifies genes modulating Notch signaling in Drosophila.
Luming Ren, Dongqing Mo, Yunlong Li, Tong Liu, Huan Yin, Na Jiang, Junzheng Zhang. PLoS One 2018
6
16

Role of JNK in a Trp53-dependent mouse model of breast cancer.
Cristina Cellurale, Claire R Weston, Judith Reilly, David S Garlick, D Joseph Jerry, Hayla K Sluss, Roger J Davis. PLoS One 2010
34
11

Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family.
Muhammad Imran Naseer, Mahmood Rasool, Angham Abdulrahman Abdulkareem, Adeel G Chaudhary, Syed Kashif Zaidi, Mohammad H Al-Qahtani. Pak J Med Sci 2019
4
25

c-Jun N-terminal kinase signaling pathway in excitotoxic cell death following kainic acid-induced status epilepticus.
Giada Spigolon, Carlo Veronesi, Christophe Bonny, Alessandro Vercelli. Eur J Neurosci 2010
46
11

Centriolar satellites assemble centrosomal microcephaly proteins to recruit CDK2 and promote centriole duplication.
Andrew Kodani, Timothy W Yu, Jeffrey R Johnson, Divya Jayaraman, Tasha L Johnson, Lihadh Al-Gazali, Lāszló Sztriha, Jennifer N Partlow, Hanjun Kim, Alexis L Krup,[...]. Elife 2015
86
11


LINC00958 Accelerates Cell Proliferation and Migration in Non-Small Cell Lung Cancer Through JNK/c-JUN Signaling.
Zhigang Luo, Zhiyi Han, Feng Shou, Yangchao Li, Yang Chen. Hum Gene Ther Methods 2019
13
11

Regulation of primordial follicle assembly and development.
Michael K Skinner. Hum Reprod Update 2005
312
11

JNK regulates lifespan in Caenorhabditis elegans by modulating nuclear translocation of forkhead transcription factor/DAF-16.
Seung Wook Oh, Arnab Mukhopadhyay, Nenad Svrzikapa, Feng Jiang, Roger J Davis, Heidi A Tissenbaum. Proc Natl Acad Sci U S A 2005
373
11

The Role of WD40-Repeat Protein 62 (MCPH2) in Brain Growth: Diverse Molecular and Cellular Mechanisms Required for Cortical Development.
Belal Shohayeb, Nicholas Rui Lim, Uda Ho, Zhiheng Xu, Mirella Dottori, Leonie Quinn, Dominic Chi Hiung Ng. Mol Neurobiol 2018
18
11



A Novel c-Jun N-terminal Kinase (JNK) Signaling Complex Involved in Neuronal Migration during Brain Development.
Feng Zhang, Jingwen Yu, Tao Yang, Dan Xu, Zhixia Chi, Yanheng Xia, Zhiheng Xu. J Biol Chem 2016
25
11

JNK signaling regulates E-cadherin junctions in germline cysts and determines primordial follicle formation in mice.
Wanbao Niu, Ye Wang, Zhengpin Wang, Qiliang Xin, Yijing Wang, Lizhao Feng, Lihua Zhao, Jia Wen, Hua Zhang, Chao Wang,[...]. Development 2016
23
11

The Thioredoxin System is Regulated by the ASK-1/JNK/p38/Survivin Pathway During Germ Cell Apoptosis.
Nora Al-Kandari, Fatemah Fadel, Farah Al-Saleh, Farah Khashab, May Al-Maghrebi. Molecules 2019
10
11

Small peptide inhibitor of JNK3 protects dopaminergic neurons from MPTP induced injury via inhibiting the ASK1-JNK3 signaling pathway.
Jing Pan, Hui Li, Bei Zhang, Ran Xiong, Yu Zhang, Wen-Yan Kang, Wei Chen, Zong-Bo Zhao, Sheng-Di Chen. PLoS One 2015
13
11

The role of c-Jun N-terminal kinase (JNK) in Parkinson's disease.
Jun Peng, Julie K Andersen. IUBMB Life 2003
65
11

Electroacupuncture Ameliorates Cognitive Impairment by Inhibiting the JNK Signaling Pathway in a Mouse Model of Alzheimer's Disease.
Yinshan Tang, Anping Xu, Shujun Shao, You Zhou, Bing Xiong, Zhigang Li. Front Aging Neurosci 2020
11
11


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.