A citation-based method for searching scientific literature

M Guipponi, F Santoni, M Schneider, C Gehrig, X B Bustillo, W R Kates, B Morrow, M Armando, S Vicari, F Sloan-Béna, M Gagnebin, V Shashi, S R Hooper, S Eliez, S E Antonarakis. Transl Psychiatry 2017
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome.
Daniele Merico, Mehdi Zarrei, Gregory Costain, Lucas Ogura, Babak Alipanahi, Matthew J Gazzellone, Nancy J Butcher, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Eva W C Chow,[...]. G3 (Bethesda) 2015
32
42

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
408
42

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Anne S Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W C Chow, Therese van Amelsvoort, Donna McDonald-McGinn, Raquel E Gur, Ann Swillen, Marianne Van den Bree,[...]. Am J Psychiatry 2017
42
42

Psychiatric disorders and intellectual functioning throughout development in velocardiofacial (22q11.2 deletion) syndrome.
Tamar Green, Doron Gothelf, Bronwyn Glaser, Martin Debbane, Amos Frisch, Moshe Kotler, Abraham Weizman, Stephan Eliez. J Am Acad Child Adolesc Psychiatry 2009
195
28

The GeneMANIA prediction server: biological network integration for gene prioritization and predicting gene function.
David Warde-Farley, Sylva L Donaldson, Ovi Comes, Khalid Zuberi, Rashad Badrawi, Pauline Chao, Max Franz, Chris Grouios, Farzana Kazi, Christian Tannus Lopes,[...]. Nucleic Acids Res 2010
28


Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study.
Louise K Hoeffding, Betina B Trabjerg, Line Olsen, Wiktor Mazin, Thomas Sparsø, Anders Vangkilde, Preben B Mortensen, Carsten B Pedersen, Thomas Werge. JAMA Psychiatry 2017
54
28

Schizophrenia two-hit hypothesis in velo-cardio facial syndrome.
Hywel J Williams, Stephen Monks, Kieran C Murphy, George Kirov, Michael C O'Donovan, Michael J Owen. Am J Med Genet B Neuropsychiatr Genet 2013
18
28

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
411
28

Developmental trajectories in 22q11.2 deletion.
Ann Swillen, Donna McDonald-McGinn. Am J Med Genet C Semin Med Genet 2015
83
28

Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.
Vandana Shashi, Matcheri Keshavan, Jessica Kaczorowski, Kelly Schoch, Kathryn E Lewandowski, Allyn McConkie-Rosell, Stephen R Hooper, Thomas R Kwapil. J Genet Couns 2010
19
14

Cortical gyrification in velo-cardio-facial (22q11.2 deletion) syndrome: a longitudinal study.
Arun Kunwar, Seethalakshmi Ramanathan, Joshua Nelson, Kevin M Antshel, Wanda Fremont, Anne Marie Higgins, Robert J Shprintzen, Wendy R Kates. Schizophr Res 2012
26
14

Structural abnormalities in cortical volume, thickness, and surface area in 22q11.2 microdeletion syndrome: Relationship with psychotic symptoms.
Maria Jalbrzikowski, Rachel Jonas, Damla Senturk, Arati Patel, Carolyn Chow, Michael F Green, Carrie E Bearden. Neuroimage Clin 2013
68
14

Association of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.
T M Allen, J Hersh, K Schoch, K Curtiss, S R Hooper, V Shashi. J Intellect Disabil Res 2014
9
14

Academic, Foundation, and Industry Collaboration in Finding New Therapies.
Bonnie W Ramsey, Gerald T Nepom, Sagar Lonial. N Engl J Med 2017
37
14

Mapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome.
Wendy R Kates, Ravi Bansal, Wanda Fremont, Kevin M Antshel, Xuejun Hao, Anne Marie Higgins, Jun Liu, Robert J Shprintzen, Bradley S Peterson. J Am Acad Child Adolesc Psychiatry 2011
23
14

WEB-based GEne SeT AnaLysis Toolkit (WebGestalt): update 2013.
Jing Wang, Dexter Duncan, Zhiao Shi, Bing Zhang. Nucleic Acids Res 2013
14

Neonatal DNA methylation patterns associate with gestational age.
James W Schroeder, Karen N Conneely, Joseph C Cubells, Varun Kilaru, D Jeffrey Newport, Bettina T Knight, Zachary N Stowe, Patricia A Brennan, Julia Krushkal, Frances A Tylavsky,[...]. Epigenetics 2011
71
14

Epigenetic mechanisms in neurological disease.
Mira Jakovcevski, Schahram Akbarian. Nat Med 2012
251
14

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur,[...]. J Med Genet 1997
821
14


The facial phenotype of the velo-cardio-facial syndrome.
Sydney C Butts. Int J Pediatr Otorhinolaryngol 2009
21
14


Functional interaction of megalin with the megalinbinding protein (MegBP), a novel tetratrico peptide repeat-containing adaptor molecule.
Helle Heibroch Petersen, Jan Hilpert, Daniel Militz, Valerie Zandler, Christian Jacobsen, Anton J M Roebroek, Thomas E Willnow. J Cell Sci 2003
40
14

Cardiac defects and results of cardiac surgery in 22q11.2 deletion syndrome.
Adriano Carotti, Maria Cristina Digilio, Gerardo Piacentini, Claudia Saffirio, Roberto M Di Donato, Bruno Marino. Dev Disabil Res Rev 2008
80
14

The ubiquitin E3 ligase NOSIP modulates protein phosphatase 2A activity in craniofacial development.
Meike Hoffmeister, Carola Prelle, Philipp Küchler, Igor Kovacevic, Markus Moser, Werner Müller-Esterl, Stefanie Oess. PLoS One 2014
13
14

The Danish 22q11 research initiative.
Henriette Schmock, Anders Vangkilde, Kit Melissa Larsen, Elvira Fischer, Michelle Rosgaard Birknow, Jens Richardt Møllegaard Jepsen, Charlotte Olesen, Flemming Skovby, Kerstin Jessica Plessen, Morten Mørup,[...]. BMC Psychiatry 2015
9
14

DNA methylation arrays as surrogate measures of cell mixture distribution.
Eugene Andres Houseman, William P Accomando, Devin C Koestler, Brock C Christensen, Carmen J Marsit, Heather H Nelson, John K Wiencke, Karl T Kelsey. BMC Bioinformatics 2012
14

Methylomic trajectories across human fetal brain development.
Helen Spiers, Eilis Hannon, Leonard C Schalkwyk, Rebecca Smith, Chloe C Y Wong, Michael C O'Donovan, Nicholas J Bray, Jonathan Mill. Genome Res 2015
158
14

Brain-specific epigenetic markers of schizophrenia.
L F Wockner, C P Morris, E P Noble, B R Lawford, V L J Whitehall, R M Young, J Voisey. Transl Psychiatry 2015
29
14


Localization of the active type I DNA topoisomerase gene on human chromosome 20q11.2-13.1, and two pseudogenes on chromosomes 1q23-24 and 22q11.2-13.1.
N Kunze, G C Yang, Z Y Jiang, H Hameister, S Adolph, K H Wiedorn, A Richter, R Knippers. Hum Genet 1989
62
14


Adjusting batch effects in microarray expression data using empirical Bayes methods.
W Evan Johnson, Cheng Li, Ariel Rabinovic. Biostatistics 2007
14

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
343
14

Nitric oxide synthase (NOS)-interacting protein interacts with neuronal NOS and regulates its distribution and activity.
Jacqueline Dreyer, Michael Schleicher, Anke Tappe, Kirstin Schilling, Thomas Kuner, Grace Kusumawidijaja, Werner Müller-Esterl, Stefanie Oess, Rohini Kuner. J Neurosci 2004
53
14

Schizophrenia-associated methylomic variation: molecular signatures of disease and polygenic risk burden across multiple brain regions.
Joana Viana, Eilis Hannon, Emma Dempster, Ruth Pidsley, Ruby Macdonald, Olivia Knox, Helen Spiers, Claire Troakes, Safa Al-Saraj, Gustavo Turecki,[...]. Hum Mol Genet 2017
55
14


The velo-cardio-facial syndrome: the spectrum of psychiatric problems and cognitive deterioration at adult age.
L J M Evers, C E M De Die-Smulders, E E J Smeets, M G M Clerkx, L M G Curfs. Genet Couns 2009
16
14

The Danish Psychiatric Central Research Register.
Ole Mors, Gurli P Perto, Preben Bo Mortensen. Scand J Public Health 2011
871
14

The annual incidence of DiGeorge/velocardiofacial syndrome.
K Devriendt, J P Fryns, G Mortier, M N van Thienen, K Keymolen. J Med Genet 1998
257
14

Nucleated red blood cell counts in the first week of life: a critical appraisal of relationships with perinatal outcome in preterm growth-restricted neonates.
Ahmet A Baschat, Sadettin Gungor, Michelle L Kush, Christoph Berg, Ulrich Gembruch, Christopher R Harman. Am J Obstet Gynecol 2007
27
14

ChAMP: 450k Chip Analysis Methylation Pipeline.
Tiffany J Morris, Lee M Butcher, Andrew Feber, Andrew E Teschendorff, Ankur R Chakravarthy, Tomasz K Wojdacz, Stephan Beck. Bioinformatics 2014
416
14


Copy number variation in schizophrenia in Sweden.
J P Szatkiewicz, C O'Dushlaine, G Chen, K Chambert, J L Moran, B M Neale, M Fromer, D Ruderfer, S Akterin, S E Bergen,[...]. Mol Psychiatry 2014
164
14

Mutations in LRP2, which encodes the multiligand receptor megalin, cause Donnai-Barrow and facio-oculo-acoustico-renal syndromes.
Sibel Kantarci, Lihadh Al-Gazali, R Sean Hill, Dian Donnai, Graeme C M Black, Eric Bieth, Nicolas Chassaing, Didier Lacombe, Koen Devriendt, Ahmad Teebi,[...]. Nat Genet 2007
204
14

Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability.
Nasim Vasli, Iltaf Ahmed, Kirti Mittal, Mehrnaz Ohadi, Anna Mikhailov, Muhammad A Rafiq, Attya Bhatti, Melissa T Carter, Danielle M Andrade, Muhammad Ayub,[...]. Psychiatr Genet 2016
11
14


Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23.
Emma Strong, Darci T Butcher, Rajat Singhania, Carolyn B Mervis, Colleen A Morris, Daniel De Carvalho, Rosanna Weksberg, Lucy R Osborne. Am J Hum Genet 2015
40
14

Methylomic profiling of human brain tissue supports a neurodevelopmental origin for schizophrenia.
Ruth Pidsley, Joana Viana, Eilis Hannon, Helen Spiers, Claire Troakes, Safa Al-Saraj, Naguib Mechawar, Gustavo Turecki, Leonard C Schalkwyk, Nicholas J Bray,[...]. Genome Biol 2014
95
14


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.