A citation-based method for searching scientific literature

Blake C Ballif, Aaron Theisen, Justine Coppinger, Gordon C Gowans, Joseph H Hersh, Suneeta Madan-Khetarpal, Karen R Schmidt, Raymond Tervo, Luis F Escobar, Christopher A Friedrich, Marie McDonald, Lindsey Campbell, Jeffrey E Ming, Elaine H Zackai, Bassem A Bejjani, Lisa G Shaffer. Mol Cytogenet 2008
Times Cited: 162



Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green, Orah S Platt, Douglas M Ruderfer, Christopher A Walsh, David Altshuler, Aravinda Chakravarti, Rudolph E Tanzi, Kari Stefansson, Susan L Santangelo, James F Gusella, Pamela Sklar, Bai-Lin Wu, Mark J Daly. N Engl J Med 2008
Times Cited: 1089




List of shared articles



Times cited

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.
Ana I Silva, Magnus O Ulfarsson, Hreinn Stefansson, Omar Gustafsson, G Bragi Walters, David E J Linden, Lawrence S Wilkinson, Mark Drakesmith, Michael J Owen, Jeremy Hall,[...]. Biol Psychiatry 2019
18


Excess of rare novel loss-of-function variants in synaptic genes in schizophrenia and autism spectrum disorders.
E M Kenny, P Cormican, S Furlong, E Heron, G Kenny, C Fahey, E Kelleher, S Ennis, D Tropea, R Anney,[...]. Mol Psychiatry 2014
113

Genetic studies in Drosophila and humans support a model for the concerted function of CISD2, PPT1 and CLN3 in disease.
Melanie A Jones, Sami Amr, Aerial Ferebee, Phung Huynh, Jill A Rosenfeld, Michael F Miles, Andrew G Davies, Christopher A Korey, John M Warrick, Rita Shiang,[...]. Biol Open 2014
8

Patient with dup(5)(q35.2-q35.3) reciprocal to the common Sotos syndrome deletion and review of the literature.
Olga Žilina, Tiia Reimand, Pille Tammur, Vallo Tillmann, Ants Kurg, Katrin Õunap. Eur J Med Genet 2013
7

Microdeletion syndromes.
Gemma L Carvill, Heather C Mefford. Curr Opin Genet Dev 2013
28

Genetic architecture of reciprocal CNVs.
Christelle Golzio, Nicholas Katsanis. Curr Opin Genet Dev 2013
32

Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk?
Claire Amiet, Isabelle Gourfinkel-An, Claudine Laurent, Nicolas Bodeau, Bérengère Génin, Eric Leguern, Sylvie Tordjman, David Cohen. Mol Autism 2013
25

Microdeletion and microduplication syndromes.
Lisenka E L M Vissers, Paweł Stankiewicz. Methods Mol Biol 2012
41

Proximal microdeletions and microduplications of 1q21.1 contribute to variable abnormal phenotypes.
Jill A Rosenfeld, Ryan N Traylor, G Bradley Schaefer, Elizabeth W McPherson, Blake C Ballif, Eva Klopocki, Stefan Mundlos, Lisa G Shaffer, Arthur S Aylsworth. Eur J Hum Genet 2012
63

Genomics, intellectual disability, and autism.
Heather C Mefford, Mark L Batshaw, Eric P Hoffman. N Engl J Med 2012
181


The genetic variability and commonality of neurodevelopmental disease.
Bradley P Coe, Santhosh Girirajan, Evan E Eichler. Am J Med Genet C Semin Med Genet 2012
74

Rare copy number variants in neuropsychiatric disorders: Specific phenotype or not?
Maarten J Van Den Bossche, Mandy Johnstone, Mojca Strazisar, Benjamin S Pickard, Dirk Goossens, An-Sofie Lenaerts, Sonia De Zutter, Annelie Nordin, Karl-Fredrik Norrback, Julien Mendlewicz,[...]. Am J Med Genet B Neuropsychiatr Genet 2012
26


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
357

Genomic structural variation in psychiatric disorders.
James J H Rucker, Peter McGuffin. Dev Psychopathol 2012
9


Rethinking the genetic architecture of schizophrenia.
K J Mitchell, D J Porteous. Psychol Med 2011
42


Copy number variants: a new molecular frontier in clinical psychiatry.
Daniel Moreno-De-Luca, Joseph F Cubells. Curr Psychiatry Rep 2011
7

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
Douglas F Levinson, Jubao Duan, Sang Oh, Kai Wang, Alan R Sanders, Jianxin Shi, Nancy Zhang, Bryan J Mowry, Ann Olincy, Farooq Amin,[...]. Am J Psychiatry 2011
316

Uncovering recurrent microdeletion syndromes and subtelomeric deletions/duplications through non-selective application of a MLPA-based extended prenatal panel in routine prenatal diagnosis.
Christopher Konialis, Birgitta Hagnefelt, Sophia Sevastidou, Sophia Karapanou, Katerina Pispili, Aggeliki Markaki, Constantinos Pangalos. Prenat Diagn 2011
10