A citation-based method for searching scientific literature

Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers, Janneke H Schuurs-Hoeijmakers, Alex Hoischen, Rolph Pfundt, Nik Krumm, Gemma L Carvill, Deana Li, David Amaral, Natasha Brown, Paul J Lockhart, Ingrid E Scheffer, Antonino Alberti, Marie Shaw, Rosa Pettinato, Raymond Tervo, Nicole de Leeuw, Margot R F Reijnders, Beth S Torchia, Hilde Peeters, Brian J O'Roak, Marco Fichera, Jayne Y Hehir-Kwa, Jay Shendure, Heather C Mefford, Eric Haan, Jozef Gécz, Bert B A de Vries, Corrado Romano, Evan E Eichler. Nat Genet 2014
Times Cited: 316



Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
Times Cited: 625




List of shared articles



Times cited

A study of normal copy number variations in Israeli population.
Idit Maya, Pola Smirin-Yosef, Sarit Kahana, Sne Morag, Shiri Yacobson, Ifaat Agmon-Fishman, Reut Matar, Elisheva Bitton, Mordechai Shohat, Lina Basel-Salmon,[...]. Hum Genet 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

CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.
Elena A Repnikova, Dmitry A Lyalin, Kimberly McDonald, Caroline Astbury, Emily Hansen-Kiss, Linda D Cooley, Ruthann Pfau, Gail E Herman, Robert E Pyatt, Scott E Hickey. Eur J Med Genet 2020
2

The genetics of intellectual disability: advancing technology and gene editing.
Muhammad Ilyas, Asif Mir, Stephanie Efthymiou, Henry Houlden. F1000Res 2020
9

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
1

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


Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity.
Gregory Costain, Susan Walker, Maria Marano, Danielle Veenma, Meaghan Snell, Meredith Curtis, Stephanie Luca, Jason Buera, Danielle Arje, Miriam S Reuter,[...]. JAMA Netw Open 2020
6

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

Clinical significance of copy number variants involving KANK1 in patients with neurodevelopmental disorders.
Rena J Vanzo, Hope Twede, Karen S Ho, Aparna Prasad, Megan M Martin, Sarah T South, E Robert Wassman. Eur J Med Genet 2019
5