A citation-based method for searching scientific literature

Rachel M Jones, Gemma Cadby, John Blangero, Lawrence J Abraham, Andrew J O Whitehouse, Eric K Moses. Psychiatr Genet 2014
Times Cited: 42







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



Times Cited
  Times     Co-cited
Similarity


A genome-wide scan for common alleles affecting risk for autism.
Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams, Nuala Sykes, Alistair T Pagnamenta,[...]. Hum Mol Genet 2010
418
50

Macrodomain-containing proteins are new mono-ADP-ribosylhydrolases.
Florian Rosenthal, Karla L H Feijs, Emilie Frugier, Mario Bonalli, Alexandra H Forst, Ralph Imhof, Hans C Winkler, David Fischer, Amedeo Caflisch, Paul O Hassa,[...]. Nat Struct Mol Biol 2013
230
28

MACROD2 overexpression mediates estrogen independent growth and tamoxifen resistance in breast cancers.
Morassa Mohseni, Justin Cidado, Sarah Croessmann, Karen Cravero, Ashley Cimino-Mathews, Hong Yuen Wong, Rob Scharpf, Daniel J Zabransky, Abde M Abukhdeir, Joseph P Garay,[...]. Proc Natl Acad Sci U S A 2014
48
28

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Anath C Lionel, Jennifer Crosbie, Nicole Barbosa, Tara Goodale, Bhooma Thiruvahindrapuram, Jessica Rickaby, Matthew Gazzellone, Andrew R Carson, Jennifer L Howe, Zhuozhi Wang,[...]. Sci Transl Med 2011
243
23

A family of macrodomain proteins reverses cellular mono-ADP-ribosylation.
Gytis Jankevicius, Markus Hassler, Barbara Golia, Vladimir Rybin, Martin Zacharias, Gyula Timinszky, Andreas G Ladurner. Nat Struct Mol Biol 2013
228
21

The C20orf133 gene is disrupted in a patient with Kabuki syndrome.
Nicole M C Maas, Tom Van de Putte, Cindy Melotte, Annick Francis, Constance T R M Schrander-Stumpel, Damien Sanlaville, David Genevieve, Stanislas Lyonnet, Boyan Dimitrov, Koenraad Devriendt,[...]. J Med Genet 2007
48
16

Deficiency of terminal ADP-ribose protein glycohydrolase TARG1/C6orf130 in neurodegenerative disease.
Reza Sharifi, Rosa Morra, C Denise Appel, Michael Tallis, Barry Chioza, Gytis Jankevicius, Michael A Simpson, Ivan Matic, Ege Ozkan, Barbara Golia,[...]. EMBO J 2013
211
16

PLINK: a tool set for whole-genome association and population-based linkage analyses.
Shaun Purcell, Benjamin Neale, Kathe Todd-Brown, Lori Thomas, Manuel A R Ferreira, David Bender, Julian Maller, Pamela Sklar, Paul I W de Bakker, Mark J Daly,[...]. Am J Hum Genet 2007
16

No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder.
Sarah Curran, Patrick Bolton, Kinga Rozsnyai, Andreas Chiocchetti, Sabine M Klauck, Eftichia Duketis, Fritz Poustka, Sabine Schlitt, Christine M Freitag, Irene Lee,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
26
26

Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bucan, Joseph T Glessner, Brett S Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P Bradfield, Patrick M A Sleiman,[...]. Nature 2009
689
14

Most genetic risk for autism resides with common variation.
Trent Gaugler, Lambertus Klei, Stephan J Sanders, Corneliu A Bodea, Arthur P Goldberg, Ann B Lee, Milind Mahajan, Dina Manaa, Yudi Pawitan, Jennifer Reichert,[...]. Nat Genet 2014
649
14

Hotspots of large rare deletions in the human genome.
W Edward C Bradley, John V Raelson, Daniel Y Dubois, Eric Godin, Hélène Fournier, Charles Privé, René Allard, Vadym Pinchuk, Micheline Lapalme, René J A Paulussen,[...]. PLoS One 2010
44
14


Identification of macrodomain proteins as novel O-acetyl-ADP-ribose deacetylases.
Dawei Chen, Melanie Vollmar, Marianna N Rossi, Claire Phillips, Rolf Kraehenbuehl, Dea Slade, Pawan V Mehrotra, Frank von Delft, Susan K Crosthwaite, Opher Gileadi,[...]. J Biol Chem 2011
121
14

Macrodomain-containing proteins: regulating new intracellular functions of mono(ADP-ribosyl)ation.
Karla L H Feijs, Alexandra H Forst, Patricia Verheugd, Bernhard Lüscher. Nat Rev Mol Cell Biol 2013
111
14

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
14

MACROD2 Haploinsufficiency Impairs Catalytic Activity of PARP1 and Promotes Chromosome Instability and Growth of Intestinal Tumors.
Anuratha Sakthianandeswaren, Marie J Parsons, Dmitri Mouradov, Ruth N MacKinnon, Bruno Catimel, Sheng Liu, Michelle Palmieri, Christopher Love, Robert N Jorissen, Shan Li,[...]. Cancer Discov 2018
28
21

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
11

A genome-wide linkage and association scan reveals novel loci for autism.
Lauren A Weiss, Dan E Arking, Mark J Daly, Aravinda Chakravarti. Nature 2009
428
11

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
11

Discovery and Replication of Gene Influences on Brain Structure Using LASSO Regression.
Omid Kohannim, Derrek P Hibar, Jason L Stein, Neda Jahanshad, Xue Hua, Priya Rajagopalan, Arthur W Toga, Clifford R Jack, Michael W Weiner, Greig I de Zubicaray,[...]. Front Neurosci 2012
64
11

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
595
11

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
11


Family-wide analysis of poly(ADP-ribose) polymerase activity.
Sejal Vyas, Ivan Matic, Lilen Uchima, Jenny Rood, Roko Zaja, Ronald T Hay, Ivan Ahel, Paul Chang. Nat Commun 2014
303
11

The structure and catalytic mechanism of a poly(ADP-ribose) glycohydrolase.
Dea Slade, Mark S Dunstan, Eva Barkauskaite, Ria Weston, Pierre Lafite, Neil Dixon, Marijan Ahel, David Leys, Ivan Ahel. Nature 2011
256
11

Loss of poly(ADP-ribose) glycohydrolase causes progressive neurodegeneration in Drosophila melanogaster.
Shuji Hanai, Masayuki Kanai, Sayaka Ohashi, Keiji Okamoto, Mitsunori Yamada, Hitoshi Takahashi, Masanao Miwa. Proc Natl Acad Sci U S A 2004
162
11

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
11

Elucidating the genetic architecture of familial schizophrenia using rare copy number variant and linkage scans.
Bin Xu, Abigail Woodroffe, Laura Rodriguez-Murillo, J Louw Roos, Elizabeth J van Rensburg, Gonçalo R Abecasis, Joseph A Gogos, Maria Karayiorgou. Proc Natl Acad Sci U S A 2009
106
11

A genome-wide survey of transgenerational genetic effects in autism.
Kathryn M Tsang, Lisa A Croen, Anthony R Torres, Martin Kharrazi, Gerald N Delorenze, Gayle C Windham, Cathleen K Yoshida, Ousseny Zerbo, Lauren A Weiss. PLoS One 2013
39
12

Serine ADP-ribosylation reversal by the hydrolase ARH3.
Pietro Fontana, Juan José Bonfiglio, Luca Palazzo, Edward Bartlett, Ivan Matic, Ivan Ahel. Elife 2017
130
11

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
780
11

A noncoding RNA antisense to moesin at 5p14.1 in autism.
Tara Kerin, Anita Ramanathan, Kasey Rivas, Nicole Grepo, Gerhard A Coetzee, Daniel B Campbell. Sci Transl Med 2012
96
9

Genome-wide association studies of MRI-defined brain infarcts: meta-analysis from the CHARGE Consortium.
Stéphanie Debette, Joshua C Bis, Myriam Fornage, Helena Schmidt, M Arfan Ikram, Sigurdur Sigurdsson, Gerardo Heiss, Maksim Struchalin, Albert V Smith, Aad van der Lugt,[...]. Stroke 2010
66
9

Analysis of CHRNA7 rare variants in autism spectrum disorder susceptibility.
Elena Bacchelli, Agatino Battaglia, Cinzia Cameli, Silvia Lomartire, Raffaella Tancredi, Susanne Thomson, James S Sutcliffe, Elena Maestrini. Am J Med Genet A 2015
33
12

The macro domain is an ADP-ribose binding module.
Georgios I Karras, Georg Kustatscher, Heeran R Buhecha, Mark D Allen, Céline Pugieux, Fiona Sait, Mark Bycroft, Andreas G Ladurner. EMBO J 2005
372
9

The single-macro domain protein LRP16 is an essential cofactor of androgen receptor.
J Yang, Y-L Zhao, Z-Q Wu, Y-L Si, Y-G Meng, X-B Fu, Y-M Mu, W-D Han. Endocr Relat Cancer 2009
39
10

SIRT4 inhibits glutamate dehydrogenase and opposes the effects of calorie restriction in pancreatic beta cells.
Marcia C Haigis, Raul Mostoslavsky, Kevin M Haigis, Kamau Fahie, Danos C Christodoulou, Andrew J Murphy, David M Valenzuela, George D Yancopoulos, Margaret Karow, Gil Blander,[...]. Cell 2006
848
9

A macrodomain-containing histone rearranges chromatin upon sensing PARP1 activation.
Gyula Timinszky, Susanne Till, Paul O Hassa, Michael Hothorn, Georg Kustatscher, Bianca Nijmeijer, Julien Colombelli, Matthias Altmeyer, Ernst H K Stelzer, Klaus Scheffzek,[...]. Nat Struct Mol Biol 2009
341
9

Rapid evolution of PARP genes suggests a broad role for ADP-ribosylation in host-virus conflicts.
Matthew D Daugherty, Janet M Young, Julie A Kerns, Harmit S Malik. PLoS Genet 2014
106
9

Toward a unified nomenclature for mammalian ADP-ribosyltransferases.
Michael O Hottiger, Paul O Hassa, Bernhard Lüscher, Herwig Schüler, Friedrich Koch-Nolte. Trends Biochem Sci 2010
611
9

Substrate-assisted catalysis by PARP10 limits its activity to mono-ADP-ribosylation.
Henning Kleine, Elzbieta Poreba, Krzysztof Lesniewicz, Paul O Hassa, Michael O Hottiger, David W Litchfield, Brian H Shilton, Bernhard Lüscher. Mol Cell 2008
253
9

LRP16 integrates into NF-κB transcriptional complex and is required for its functional activation.
Zhiqiang Wu, Yazhuo Li, Xiaolei Li, Dongdong Ti, Yali Zhao, Yiling Si, Qian Mei, Po Zhao, Xiaobing Fu, Weidong Han. PLoS One 2011
33
12

Processing of protein ADP-ribosylation by Nudix hydrolases.
Luca Palazzo, Benjamin Thomas, Ann-Sofie Jemth, Thomas Colby, Orsolya Leidecker, Karla L H Feijs, Roko Zaja, Olga Loseva, Jordi Carreras Puigvert, Ivan Matic,[...]. Biochem J 2015
94
9

ARTD10 substrate identification on protein microarrays: regulation of GSK3β by mono-ADP-ribosylation.
Karla Lh Feijs, Henning Kleine, Anne Braczynski, Alexandra H Forst, Nicolas Herzog, Patricia Verheugd, Ulrike Linzen, Elisabeth Kremmer, Bernhard Lüscher. Cell Commun Signal 2013
97
9

Poly(ADP-ribose) regulates stress responses and microRNA activity in the cytoplasm.
Anthony K L Leung, Sejal Vyas, Jennifer E Rood, Arjun Bhutkar, Phillip A Sharp, Paul Chang. Mol Cell 2011
310
9

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
9

An eQTL mapping approach reveals that rare variants in the SEMA5A regulatory network impact autism risk.
Ye Cheng, Jeffrey Francis Quinn, Lauren Anne Weiss. Hum Mol Genet 2013
40
10

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population.
Elise B Robinson, Beate St Pourcain, Verneri Anttila, Jack A Kosmicki, Brendan Bulik-Sullivan, Jakob Grove, Julian Maller, Kaitlin E Samocha, Stephan J Sanders, Stephan Ripke,[...]. Nat Genet 2016
231
9

Macrodomains: Structure, Function, Evolution, and Catalytic Activities.
Johannes Gregor Matthias Rack, Dragutin Perina, Ivan Ahel. Annu Rev Biochem 2016
139
9


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.