A citation-based method for searching scientific literature

Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig, Hoda Abdel-Hamid, Patricia Bader, Elizabeth McCracken, Dmitriy Niyazov, Kathleen Leppig, Heidi Thiese, Marybeth Hummel, Nora Alexander, Jerome Gorski, Jennifer Kussmann, Vandana Shashi, Krys Johnson, Catherine Rehder, Blake C Ballif, Lisa G Shaffer, Evan E Eichler. Nat Genet 2011
Times Cited: 778



Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
Times Cited: 603




List of shared articles



Times cited

Copy Number Variants and Polygenic Risk Scores Predict Need of Care in Autism and/or ADHD Families.
Sonja LaBianca, Jette LaBianca, Anne Katrine Pagsberg, Klaus Damgaard Jakobsen, Vivek Appadurai, Alfonso Buil, Thomas Werge. J Autism Dev Disord 2021
1


Cell-free tumour DNA analysis detects copy number alterations in gastro-oesophageal cancer patients.
Karin Wallander, Jesper Eisfeldt, Mats Lindblad, Daniel Nilsson, Kenny Billiau, Hassan Foroughi, Magnus Nordenskjöld, Agne Liedén, Emma Tham. PLoS One 2021
0

Novel MYT1 variants expose the complexity of oculo-auriculo-vertebral spectrum genetic mechanisms.
Malú Zamariolli, Bruna Burssed, Mariana Moysés-Oliveira, Mileny Colovati, Fernanda Teixeira da Silva Bellucco, Leonardo Caires Dos Santos, Ana Beatriz Alvarez Perez, Silvia Bragagnolo, Maria Isabel Melaragno. Am J Med Genet A 2021
0

Genome-wide copy number variations in a large cohort of bantu African children.
Feyza Yilmaz, Megan Null, David Astling, Hung-Chun Yu, Joanne Cole, Stephanie A Santorico, Benedikt Hallgrimsson, Mange Manyama, Richard A Spritz, Audrey E Hendricks,[...]. BMC Med Genomics 2021
0

De novo duplication on Chromosome 19 observed in nuclear family displaying neurodevelopmental disorders.
Calvin P Sjaarda, Beatrice Kaiser, Amy J M McNaughton, Melissa L Hudson, Liam Harris-Lowe, Kyle Lou, Andrea Guerin, Muhammad Ayub, Xudong Liu. Cold Spring Harb Mol Case Stud 2020
0

Mapping and characterization of structural variation in 17,795 human genomes.
Haley J Abel, David E Larson, Allison A Regier, Colby Chiang, Indraniel Das, Krishna L Kanchi, Ryan M Layer, Benjamin M Neale, William J Salerno, Catherine Reeves,[...]. Nature 2020
22

Clinical and genetic findings in Hungarian pediatric patients carrying chromosome 16p copy number variants and a review of the literature.
Anna Lengyel, Éva Pinti, Henriett Pikó, Eszter Jávorszky, Dezső David, Mariann Tihanyi, Éva Gönczi, Eszter Kiss, Zsuzsa Tóth, Kálmán Tory,[...]. Eur J Med Genet 2020
0

Copy number variation (CNV) identification, interpretation, and database from Brazilian patients.
Victória Cabral Silveira Monteiro de Godoy, Fernanda Teixeira Bellucco, Mileny Colovati, Hélio Rodrigues de Oliveira-Junior, Mariana Moysés-Oliveira, Maria Isabel Melaragno. Genet Mol Biol 2020
0

Identification of biological mechanisms underlying a multidimensional ASD phenotype using machine learning.
Muhammad Asif, Hugo F M C Martiniano, Ana Rita Marques, João Xavier Santos, Joana Vilela, Celia Rasga, Guiomar Oliveira, Francisco M Couto, Astrid M Vicente. Transl Psychiatry 2020
3

MYT1L: A systematic review of genetic variation encompassing schizophrenia and autism.
Patricia Mansfield, John N Constantino, Dustin Baldridge. Am J Med Genet B Neuropsychiatr Genet 2020
0