CoCites: A citation-based method for searching scientific literature

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication.

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: 168

CNVs conferring risk of autism or schizophrenia affect cognition in controls.

Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle, Heike Tost, Oliver Grimm, Solveig Kristjansdottir, Heimir Snorrason, Solveig R Davidsdottir, Larus J Gudmundsson, Gudbjorn F Jonsson, Berglind Stefansdottir, Isafold Helgadottir, Magnus Haraldsson, Birna Jonsdottir, Johan H Thygesen, Adam J Schwarz, Michael Didriksen, Tine B Stensbøl, Michael Brammer, Shitij Kapur, Jonas G Halldorsson, Stefan Hreidarsson, Evald Saemundsen, Engilbert Sigurdsson, Kari Stefansson. Nature 2014
Times Cited: 402

List of shared articles

Times cited

Metabolic effects of the schizophrenia-associated 3q29 deletion.
Rebecca M Pollak, Ryan H Purcell, Timothy P Rutkowski, Tamika Malone, Kimberly J Pachura, Gary J Bassell, Michael P Epstein, Paul A Dawson, Matthew R Smith, Dean P Jones,[...]. Transl Psychiatry 2022

Craniofacial features of 3q29 deletion syndrome: Application of next-generation phenotyping technology.
Bryan C Mak, Rossana Sanchez Russo, Michael J Gambello, Nicole Fleischer, Emily D Black, Elizabeth Leslie, Melissa M Murphy, Jennifer Gladys Mulle. Am J Med Genet A 2021

New phenotypes associated with 3q29 duplication syndrome: Results from the 3q29 registry.
Rebecca M Pollak, Michael C Zinsmeister, Melissa M Murphy, Michael E Zwick, Jennifer G Mulle. Am J Med Genet A 2020

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

Neuropsychiatric phenotypes and a distinct constellation of ASD features in 3q29 deletion syndrome: results from the 3q29 registry.
Rebecca M Pollak, Melissa M Murphy, Michael P Epstein, Michael E Zwick, Cheryl Klaiman, Celine A Saulnier, Jennifer G Mulle. Mol Autism 2019

Genetic variability in scaffolding proteins and risk for schizophrenia and autism-spectrum disorders: a systematic review.
Jordi Soler, Lourdes Fañanás, Mara Parellada, Marie-Odile Krebs, Guy A Rouleau, Mar Fatjó-Vilas. J Psychiatry Neurosci 2018

Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome.
Melissa M Murphy, T Lindsey Burrell, Joseph F Cubells, Roberto Antonio España, Michael J Gambello, Katrina C B Goines, Cheryl Klaiman, Longchuan Li, Derek M Novacek, Ava Papetti,[...]. BMC Psychiatry 2018

Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications.
Fátima Torres, Mafalda Barbosa, Patrícia Maciel. J Med Genet 2016

Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.
Megan R Glassford, Jill A Rosenfeld, Alexa A Freedman, Michael E Zwick, Jennifer G Mulle. Am J Med Genet A 2016

Genetics of autism spectrum disorder: an update on copy number variations leading to autism in the next generation sequencing era.
Maysoon AlSagob, Dilek Colak, Namik Kaya. Discov Med 2015