A citation-based method for searching scientific literature

Jokthan Guivarch, Clarisse Chatel, Jeremie Mortreux, Chantal Missirian, Nicole Philip, François Poinso. J Med Case Rep 2018
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Neuroleptic drugs in dementia: benefits and harm.
Clive Ballard, Robert Howard. Nat Rev Neurosci 2006
173
100

Psychosis in Alzheimer's disease.
Patrick S Murray, Sanjeev Kumar, Mary Ann A Demichele-Sweet, Robert A Sweet. Biol Psychiatry 2014
84
100

A rare missense variant in RCL1 segregates with depression in extended families.
N Amin, F M S de Vrij, M Baghdadi, R W W Brouwer, J G J van Rooij, O Jovanova, A G Uitterlinden, A Hofman, H L A Janssen, S Darwish Murad,[...]. Mol Psychiatry 2018
18
100

Rcl1 protein, a novel nuclease for 18 S ribosomal RNA production.
Darryl M Horn, Saundra L Mason, Katrin Karbstein. J Biol Chem 2011
46
100

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
100

A large data resource of genomic copy number variation across neurodevelopmental disorders.
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, Edwin J Young, Edward J Higginbotham, Jeffrey R MacDonald, Brett Trost, Ada J S Chan, Susan Walker, Sylvia Lamoureux,[...]. NPJ Genom Med 2019
31
100

Genome-wide association meta-analysis of neuropathologic features of Alzheimer's disease and related dementias.
Gary W Beecham, Kara Hamilton, Adam C Naj, Eden R Martin, Matt Huentelman, Amanda J Myers, Jason J Corneveaux, John Hardy, Jean-Paul Vonsattel, Steven G Younkin,[...]. PLoS Genet 2014
185
100


A data-driven investigation of relationships between bipolar psychotic symptoms and schizophrenia genome-wide significant genetic loci.
Ganna Leonenko, Arianna Di Florio, Judith Allardyce, Liz Forty, Sarah Knott, Lisa Jones, Katherine Gordon-Smith, Michael J Owen, Ian Jones, James Walters,[...]. Am J Med Genet B Neuropsychiatr Genet 2018
7
100

When ribosomes go bad: diseases of ribosome biogenesis.
Emily F Freed, Franziska Bleichert, Laura M Dutca, Susan J Baserga. Mol Biosyst 2010
112
100

Ribosomopathies: how a common root can cause a tree of pathologies.
Nadia Danilova, Hanna T Gazda. Dis Model Mech 2015
96
100

Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Ziv Gan-Or, Naima Bouslam, Nazha Birouk, Alexandra Lissouba, Daniel B Chambers, Julie Vérièpe, Alaura Androschuk, Sandra B Laurent, Daniel Rochefort, Dan Spiegelman,[...]. Am J Hum Genet 2016
56
100

16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
Kyle J Steinman, Sarah J Spence, Melissa B Ramocki, Monica B Proud, Sudha K Kessler, Elysa J Marco, LeeAnne Green Snyder, Debra D'Angelo, Qixuan Chen, Wendy K Chung,[...]. Am J Med Genet A 2016
70
100

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Catherine A Brownstein, Alan H Beggs, Nils Homer, Barry Merriman, Timothy W Yu, Katherine C Flannery, Elizabeth T DeChene, Meghan C Towne, Sarah K Savage, Emily N Price,[...]. Genome Biol 2014
73
100

A meta-analysis of nonsense mutations causing human genetic disease.
Matthew Mort, Dobril Ivanov, David N Cooper, Nadia A Chuzhanova. Hum Mutat 2008
187
100

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
516
100

Seventy-five genetic loci influencing the human red blood cell.
Pim van der Harst, Weihua Zhang, Irene Mateo Leach, Augusto Rendon, Niek Verweij, Joban Sehmi, Dirk S Paul, Ulrich Elling, Hooman Allayee, Xinzhong Li,[...]. Nature 2012
221
100

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
398
100

Crucial role of the Rcl1p-Bms1p interaction for yeast pre-ribosomal RNA processing.
Anna Delprato, Yasmine Al Kadri, Natacha Pérébaskine, Cécile Monfoulet, Yves Henry, Anthony K Henras, Sébastien Fribourg. Nucleic Acids Res 2014
18
100

The economics of ribosome biosynthesis in yeast.
J R Warner. Trends Biochem Sci 1999
100

From genetics to biology: advancing mental health research in the Genomics ERA.
P Alexander Arguello, Anjené Addington, Susan Borja, Linda Brady, Tara Dutka, Miri Gitik, Susan Koester, Douglas Meinecke, Kathleen Merikangas, Francis J McMahon,[...]. Mol Psychiatry 2019
4
100

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kimberley M Kendall, Elliott Rees, Valentina Escott-Price, Mark Einon, Rhys Thomas, Jonathan Hewitt, Michael C O'Donovan, Michael J Owen, James T R Walters, George Kirov. Biol Psychiatry 2017
74
100

Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
Kate Wolfe, Andrew McQuillin, Viola Alesi, Elise Boudry Labis, Peter Cutajar, Bruno Dallapiccola, Maria Lisa Dentici, Anne Dieux-Coeslier, Benedicte Duban-Bedu, Tina Duelund Hjortshøj,[...]. Am J Med Genet B Neuropsychiatr Genet 2018
6
100


New gene functions in megakaryopoiesis and platelet formation.
Christian Gieger, Aparna Radhakrishnan, Ana Cvejic, Weihong Tang, Eleonora Porcu, Giorgio Pistis, Jovana Serbanovic-Canic, Ulrich Elling, Alison H Goodall, Yann Labrune,[...]. Nature 2011
279
100

Rare UNC13B variations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study.
Jun Egawa, Satoshi Hoya, Yuichiro Watanabe, Ayako Nunokawa, Masako Shibuya, Masashi Ikeda, Emiko Inoue, Shujiro Okuda, Kenji Kondo, Takeo Saito,[...]. Am J Med Genet B Neuropsychiatr Genet 2016
15
100

Homozygous CAPN1 mutations causing a spastic-ataxia phenotype in 2 families.
Cemile Kocoglu, Asli Gundogdu, Gulsen Kocaman, Pinar Kahraman-Koytak, Kayihan Uluc, Gunes Kiziltan, Ahmet Okay Caglayan, Kaya Bilguvar, Atay Vural, A Nazli Basak. Neurol Genet 2018
14
100

Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and Humans.
Yubin Wang, Joshua Hersheson, Dulce Lopez, Monia Hammer, Yan Liu, Ka-Hung Lee, Vanessa Pinto, Jeff Seinfeld, Sarah Wiethoff, Jiandong Sun,[...]. Cell Rep 2016
53
100

Expanding the clinical phenotype of CAPN1-associated mutations: A new case with congenital-onset pure spastic paraplegia.
Lorena Travaglini, Emanuele Bellacchio, Chiara Aiello, Stefano Pro, Enrico Bertini, Francesco Nicita. J Neurol Sci 2017
16
100

Five novel loci associated with antipsychotic treatment response in patients with schizophrenia: a genome-wide association study.
Hao Yu, Hao Yan, Lifang Wang, Jun Li, Liwen Tan, Wei Deng, Qi Chen, Guigang Yang, Fuquan Zhang, Tianlan Lu,[...]. Lancet Psychiatry 2018
49
100

Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are risk factors for colorectal cancer.
Richarda M de Voer, Ad Geurts van Kessel, Robbert D A Weren, Marjolijn J L Ligtenberg, Dominique Smeets, Lei Fu, Lilian Vreede, Eveline J Kamping, Eugène T P Verwiel, Marc-Manuel Hahn,[...]. Gastroenterology 2013
58
100

A framework for the investigation of rare genetic disorders in neuropsychiatry.
Stephan J Sanders, Mustafa Sahin, Joseph Hostyk, Audrey Thurm, Sebastien Jacquemont, Paul Avillach, Elise Douard, Christa L Martin, Meera E Modi, Andres Moreno-De-Luca,[...]. Nat Med 2019
28
100

A genotype-first approach to defining the subtypes of a complex disease.
Holly A Stessman, Raphael Bernier, Evan E Eichler. Cell 2014
135
100

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.
Khader Shameer, Joshua C Denny, Keyue Ding, Hayan Jouni, David R Crosslin, Mariza de Andrade, Christopher G Chute, Peggy Peissig, Jennifer A Pacheco, Rongling Li,[...]. Hum Genet 2014
92
100

A Genocentric Approach to Discovery of Mendelian Disorders.
Adam W Hansen, Mullai Murugan, He Li, Michael M Khayat, Liwen Wang, Jill Rosenfeld, B Kim Andrews, Shalini N Jhangiani, Zeynep H Coban Akdemir, Fritz J Sedlazeck,[...]. Am J Hum Genet 2019
12
100

Gene expression elucidates functional impact of polygenic risk for schizophrenia.
Menachem Fromer, Panos Roussos, Solveig K Sieberts, Jessica S Johnson, David H Kavanagh, Thanneer M Perumal, Douglas M Ruderfer, Edwin C Oh, Aaron Topol, Hardik R Shah,[...]. Nat Neurosci 2016
447
100

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
506
100

A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Panos Roussos, Colm O'Dushlaine, Kimberly Chambert, Sarah E Bergen, Anna Kähler,[...]. Nature 2014
875
100

Identification of 315 genes essential for early zebrafish development.
Adam Amsterdam, Robert M Nissen, Zhaoxia Sun, Eric C Swindell, Sarah Farrington, Nancy Hopkins. Proc Natl Acad Sci U S A 2004
587
100


The Allen Brain Atlas: 5 years and beyond.
Allan R Jones, Caroline C Overly, Susan M Sunkin. Nat Rev Neurosci 2009
170
100


Examining the association between genetic liability for schizophrenia and psychotic symptoms in Alzheimer's disease.
Byron Creese, Evangelos Vassos, Sverre Bergh, Lavinia Athanasiu, Iskandar Johar, Arvid Rongve, Ingrid Tøndel Medbøen, Miguel Vasconcelos Da Silva, Eivind Aakhus, Fred Andersen,[...]. Transl Psychiatry 2019
12
100

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.
Tarjinder Singh, Mitja I Kurki, David Curtis, Shaun M Purcell, Lucy Crooks, Jeremy McRae, Jaana Suvisaari, Himanshu Chheda, Douglas Blackwood, Gerome Breen,[...]. Nat Neurosci 2016
213
100

Schizophrenia risk from complex variation of complement component 4.
Aswin Sekar, Allison R Bialas, Heather de Rivera, Avery Davis, Timothy R Hammond, Nolan Kamitaki, Katherine Tooley, Jessy Presumey, Matthew Baum, Vanessa Van Doren,[...]. Nature 2016
100

The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease.
William J Astle, Heather Elding, Tao Jiang, Dave Allen, Dace Ruklisa, Alice L Mann, Daniel Mead, Heleen Bouman, Fernando Riveros-Mckay, Myrto A Kostadima,[...]. Cell 2016
429
100

Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases.
Masahiro Kanai, Masato Akiyama, Atsushi Takahashi, Nana Matoba, Yukihide Momozawa, Masashi Ikeda, Nakao Iwata, Shiro Ikegawa, Makoto Hirata, Koichi Matsuda,[...]. Nat Genet 2018
206
100

Sodium Channel SCN3A (NaV1.3) Regulation of Human Cerebral Cortical Folding and Oral Motor Development.
Richard S Smith, Connor J Kenny, Vijay Ganesh, Ahram Jang, Rebeca Borges-Monroy, Jennifer N Partlow, R Sean Hill, Taehwan Shin, Allen Y Chen, Ryan N Doan,[...]. Neuron 2018
47
100


Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
100


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.