A citation-based method for searching scientific literature

Sandra Jansen, Sinje Geuer, Rolph Pfundt, Rachel Brough, Priyanka Ghongane, Johanna C Herkert, Elysa J Marco, Marjolein H Willemsen, Tjitske Kleefstra, Mark Hannibal, Joseph T Shieh, Sally Ann Lynch, Frances Flinter, David R FitzPatrick, Alice Gardham, Birgitta Bernhard, Nicola Ragge, Ruth Newbury-Ecob, Raphael Bernier, Malin Kvarnung, E A Helena Magnusson, Marja W Wessels, Marjon A van Slegtenhorst, Kristin G Monaghan, Petra de Vries, Joris A Veltman, Christopher J Lord, Lisenka E L M Vissers, Bert B A de Vries. Am J Hum Genet 2017
Times Cited: 27







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



Times Cited
  Times     Co-cited
Similarity


Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
33


DVL1 frameshift mutations clustering in the penultimate exon cause autosomal-dominant Robinow syndrome.
Janson White, Juliana F Mazzeu, Alexander Hoischen, Shalini N Jhangiani, Tomasz Gambin, Michele Calijorne Alcino, Samantha Penney, Jorge M Saraiva, Hanne Hove, Flemming Skovby,[...]. Am J Hum Genet 2015
69
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

DVL3 Alleles Resulting in a -1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome.
Janson J White, Juliana F Mazzeu, Alexander Hoischen, Yavuz Bayram, Marjorie Withers, Alper Gezdirici, Virginia Kimonis, Marloes Steehouwer, Shalini N Jhangiani, Donna M Muzny,[...]. Am J Hum Genet 2016
51
18

GeneMatcher: a matching tool for connecting investigators with an interest in the same gene.
Nara Sobreira, François Schiettecatte, David Valle, Ada Hamosh. Hum Mutat 2015
589
18

Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability.
Stefan H Lelieveld, Margot R F Reijnders, Rolph Pfundt, Helger G Yntema, Erik-Jan Kamsteeg, Petra de Vries, Bert B A de Vries, Marjolein H Willemsen, Tjitske Kleefstra, Katharina Löhner,[...]. Nat Neurosci 2016
219
14

The type 2C phosphatase Wip1: an oncogenic regulator of tumor suppressor and DNA damage response pathways.
Xiongbin Lu, Thuy-Ai Nguyen, Sung-Hwan Moon, Yolanda Darlington, Matthias Sommer, Lawrence A Donehower. Cancer Metastasis Rev 2008
173
14


Wip1, a novel human protein phosphatase that is induced in response to ionizing radiation in a p53-dependent manner.
M Fiscella, H Zhang, S Fan, K Sakaguchi, S Shen, W E Mercer, G F Vande Woude, P M O'Connor, E Appella. Proc Natl Acad Sci U S A 1997
408
14

Genetic studies in intellectual disability and related disorders.
Lisenka E L M Vissers, Christian Gilissen, Joris A Veltman. Nat Rev Genet 2016
311
11


A framework for the interpretation of de novo mutation in human disease.
Kaitlin E Samocha, Elise B Robinson, Stephan J Sanders, Christine Stevens, Aniko Sabo, Lauren M McGrath, Jack A Kosmicki, Karola Rehnström, Swapan Mallick, Andrew Kirby,[...]. Nat Genet 2014
511
11

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
11

A general framework for estimating the relative pathogenicity of human genetic variants.
Martin Kircher, Daniela M Witten, Preti Jain, Brian J O'Roak, Gregory M Cooper, Jay Shendure. Nat Genet 2014
11

Genome-wide atlas of gene expression in the adult mouse brain.
Ed S Lein, Michael J Hawrylycz, Nancy Ao, Mikael Ayres, Amy Bensinger, Amy Bernard, Andrew F Boe, Mark S Boguski, Kevin S Brockway, Emi J Byrnes,[...]. Nature 2007
11

Amplification of PPM1D in human tumors abrogates p53 tumor-suppressor activity.
Dmitry V Bulavin, Oleg N Demidov, Shin'ichi Saito, Paivikki Kauraniemi, Crissy Phillips, Sally A Amundson, Concetta Ambrosino, Guido Sauter, Angel R Nebreda, Carl W Anderson,[...]. Nat Genet 2002
327
11

PPM1D dephosphorylates Chk1 and p53 and abrogates cell cycle checkpoints.
Xiongbin Lu, Bonnie Nannenga, Lawrence A Donehower. Genes Dev 2005
286
11

Oncogenic properties of PPM1D located within a breast cancer amplification epicenter at 17q23.
Jing Li, Ying Yang, Yue Peng, Richard J Austin, Winfried G van Eyndhoven, Ken C Q Nguyen, Tim Gabriele, Mila E McCurrach, Jeffrey R Marks, Timothy Hoey,[...]. Nat Genet 2002
195
11

Two unrelated girls with intellectual disability associated with a truncating mutation in the PPM1D penultimate exon.
Yukiko Kuroda, Hiroaki Murakami, Takayuki Yokoi, Tatsuro Kumaki, Yumi Enomoto, Yoshinori Tsurusaki, Kenji Kurosawa. Brain Dev 2019
4
75

Novel truncating PPM1D mutation in a patient with intellectual disability.
Joseph Porrmann, Andreas Rump, Karl Hackmann, Nataliya Di Donato, Anne-Karin Kahlert, Johannes Wagner, Arne Jahn, Ines Eger, Monika Flury, Evelin Schrock,[...]. Eur J Med Genet 2019
3
100

Gain-of-function mutations of PPM1D/Wip1 impair the p53-dependent G1 checkpoint.
Petra Kleiblova, Indra A Shaltiel, Jan Benada, Jan Ševčík, Soňa Pecháčková, Petr Pohlreich, Emile E Voest, Pavel Dundr, Jiri Bartek, Zdenek Kleibl,[...]. J Cell Biol 2013
87
11

Spatial and temporal homogeneity of driver mutations in diffuse intrinsic pontine glioma.
Hamid Nikbakht, Eshini Panditharatna, Leonie G Mikael, Rui Li, Tenzin Gayden, Matthew Osmond, Cheng-Ying Ho, Madhuri Kambhampati, Eugene I Hwang, Damien Faury,[...]. Nat Commun 2016
124
11

p53-inducible wip1 phosphatase mediates a negative feedback regulation of p38 MAPK-p53 signaling in response to UV radiation.
M Takekawa, M Adachi, A Nakahata, I Nakayama, F Itoh, H Tsukuda, Y Taya, K Imai. EMBO J 2000
324
11

Exome sequencing identifies somatic gain-of-function PPM1D mutations in brainstem gliomas.
Liwei Zhang, Lee H Chen, Hong Wan, Rui Yang, Zhaohui Wang, Jie Feng, Shaohua Yang, Siân Jones, Sizhen Wang, Weixin Zhou,[...]. Nat Genet 2014
95
11

Allosteric Wip1 phosphatase inhibition through flap-subdomain interaction.
Aidan G Gilmartin, Thomas H Faitg, Mark Richter, Arthur Groy, Mark A Seefeld, Michael G Darcy, Xin Peng, Kelly Federowicz, Jingsong Yang, Shu-Yun Zhang,[...]. Nat Chem Biol 2014
116
11

Mice deficient for the wild-type p53-induced phosphatase gene (Wip1) exhibit defects in reproductive organs, immune function, and cell cycle control.
Jene Choi, Bonnie Nannenga, Oleg N Demidov, Dmitry V Bulavin, Austin Cooney, Cory Brayton, Yongxin Zhang, Innocent N Mbawuike, Allan Bradley, Ettore Appella,[...]. Mol Cell Biol 2002
135
11

WIP1 phosphatase as pharmacological target in cancer therapy.
Soňa Pecháčková, Kamila Burdová, Libor Macurek. J Mol Med (Berl) 2017
25
12

Phosphatase Wip1 controls antigen-independent B-cell development in a p53-dependent manner.
Weiwei Yi, Xuelian Hu, Zhiyang Chen, Leiming Liu, Yuan Tian, Hui Chen, Yu-Sheng Cong, Fan Yang, Lianfeng Zhang, Karl Lenhard Rudolph,[...]. Blood 2015
24
12

Chemical inhibition of Wip1 phosphatase contributes to suppression of tumorigenesis.
Galina I Belova, Oleg N Demidov, Albert J Fornace, Dmitry V Bulavin. Cancer Biol Ther 2005
60
11

Wip1-dependent regulation of autophagy, obesity, and atherosclerosis.
Xavier Le Guezennec, Anna Brichkina, Yi-Fu Huang, Elena Kostromina, Weiping Han, Dmitry V Bulavin. Cell Metab 2012
97
11

WIP1 phosphatase is a negative regulator of NF-kappaB signalling.
Joanne Chew, Subhra Biswas, Sathyavageeswaran Shreeram, Mahathir Humaidi, Ee Tsin Wong, Manprit Kaur Dhillion, Hsiangling Teo, Amit Hazra, Cheok Chit Fang, Eduardo López-Collazo,[...]. Nat Cell Biol 2009
121
11

Inactivation of the Wip1 phosphatase inhibits mammary tumorigenesis through p38 MAPK-mediated activation of the p16(Ink4a)-p19(Arf) pathway.
Dmitry V Bulavin, Crissy Phillips, Bonnie Nannenga, Oleg Timofeev, Larry A Donehower, Carl W Anderson, Ettore Appella, Albert J Fornace. Nat Genet 2004
332
11

Wip1 deficiency impairs haematopoietic stem cell function via p53 and mTORC1 pathways.
Zhiyang Chen, Weiwei Yi, Yohei Morita, Hu Wang, Yusheng Cong, Jun-Ping Liu, Zhicheng Xiao, K Lenhard Rudolph, Tao Cheng, Zhenyu Ju. Nat Commun 2015
34
11

Regulation of the antioncogenic Chk2 kinase by the oncogenic Wip1 phosphatase.
H Fujimoto, N Onishi, N Kato, M Takekawa, X Z Xu, A Kosugi, T Kondo, M Imamura, I Oishi, A Yoda,[...]. Cell Death Differ 2006
148
11

A chemical inhibitor of PPM1D that selectively kills cells overexpressing PPM1D.
S Rayter, R Elliott, J Travers, M G Rowlands, T B Richardson, K Boxall, K Jones, S Linardopoulos, P Workman, W Aherne,[...]. Oncogene 2008
66
11

Phosphatase Wip1 negatively regulates neutrophil migration and inflammation.
Bo Sun, Xuelian Hu, Guangwei Liu, Bo Ma, Yamei Xu, Tao Yang, Jianfeng Shi, Fan Yang, Hongran Li, Lianfeng Zhang,[...]. J Immunol 2014
50
11

Optimization of a cyclic peptide inhibitor of Ser/Thr phosphatase PPM1D (Wip1).
Ryo Hayashi, Kan Tanoue, Stewart R Durell, Deb K Chatterjee, Lisa M Miller Jenkins, Daniel H Appella, Ettore Appella. Biochemistry 2011
29
11

CSNK2B splice site mutations in patients cause intellectual disability with or without myoclonic epilepsy.
Karine Poirier, Laurence Hubert, Géraldine Viot, Marlène Rio, Pierre Billuart, Claude Besmond, Thierry Bienvenu. Hum Mutat 2017
16
12

Haploinsufficiency of MeCP2-interacting transcriptional co-repressor SIN3A causes mild intellectual disability by affecting the development of cortical integrity.
Josefine S Witteveen, Marjolein H Willemsen, Thaís C D Dombroski, Nick H M van Bakel, Willy M Nillesen, Josephus A van Hulten, Eric J R Jansen, Dave Verkaik, Hermine E Veenstra-Knol, Conny M A van Ravenswaaij-Arts,[...]. Nat Genet 2016
35
7

REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis.
Yavuz Bayram, Janson J White, Nursel Elcioglu, Megan T Cho, Neda Zadeh, Asuman Gedikbasi, Sukru Palanduz, Sukru Ozturk, Kivanc Cefle, Ozgur Kasapcopur,[...]. Am J Hum Genet 2017
19
10

Nonsense-mediated mRNA decay in humans at a glance.
Tatsuaki Kurosaki, Lynne E Maquat. J Cell Sci 2016
174
7

Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations.
Ken Inoue, Mehrdad Khajavi, Tomoko Ohyama, Shin-ichi Hirabayashi, John Wilson, James D Reggin, Pedro Mancias, Ian J Butler, Miles F Wilkinson, Michael Wegner,[...]. Nat Genet 2004
300
7

Dominant versus recessive traits conveyed by allelic mutations - to what extent is nonsense-mediated decay involved?
S Ben-Shachar, M Khajavi, M A Withers, C A Shaw, H van Bokhoven, H G Brunner, J R Lupski. Clin Genet 2009
21
9

Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples.
Jack A Kosmicki, Kaitlin E Samocha, Daniel P Howrigan, Stephan J Sanders, Kamil Slowikowski, Monkol Lek, Konrad J Karczewski, David J Cutler, Bernie Devlin, Kathryn Roeder,[...]. Nat Genet 2017
152
7

Heterozygous Truncating Variants in POMP Escape Nonsense-Mediated Decay and Cause a Unique Immune Dysregulatory Syndrome.
M Cecilia Poli, Frédéric Ebstein, Sarah K Nicholas, Marietta M de Guzman, Lisa R Forbes, Ivan K Chinn, Emily M Mace, Tiphanie P Vogel, Alexandre F Carisey, Felipe Benavides,[...]. Am J Hum Genet 2018
52
7

The rules and impact of nonsense-mediated mRNA decay in human cancers.
Rik G H Lindeboom, Fran Supek, Ben Lehner. Nat Genet 2016
154
7

NMD: a multifaceted response to premature translational termination.
Stephanie Kervestin, Allan Jacobson. Nat Rev Mol Cell Biol 2012
358
7

De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability.
Sébastien Küry, Geeske M van Woerden, Thomas Besnard, Martina Proietti Onori, Xénia Latypova, Meghan C Towne, Megan T Cho, Trine E Prescott, Melissa A Ploeg, Stephan Sanders,[...]. Am J Hum Genet 2017
53
7

denovo-db: a compendium of human de novo variants.
Tychele N Turner, Qian Yi, Niklas Krumm, John Huddleston, Kendra Hoekzema, Holly A F Stessman, Anna-Lisa Doebley, Raphael A Bernier, Deborah A Nickerson, Evan E Eichler. Nucleic Acids Res 2017
89
7


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.