A citation-based method for searching scientific literature

Hreinn Stefansson, Dan Rujescu, Sven Cichon, Olli P H Pietiläinen, Andres Ingason, Stacy Steinberg, Ragnheidur Fossdal, Engilbert Sigurdsson, Thordur Sigmundsson, Jacobine E Buizer-Voskamp, Thomas Hansen, Klaus D Jakobsen, Pierandrea Muglia, Clyde Francks, Paul M Matthews, Arnaldur Gylfason, Bjarni V Halldorsson, Daniel Gudbjartsson, Thorgeir E Thorgeirsson, Asgeir Sigurdsson, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Asgeir Bjornsson, Sigurborg Mattiasdottir, Thorarinn Blondal, Magnus Haraldsson, Brynja B Magnusdottir, Ina Giegling, Hans-Jürgen Möller, Annette Hartmann, Kevin V Shianna, Dongliang Ge, Anna C Need, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lonnqvist, Jaana Suvisaari, Annamarie Tuulio-Henriksson, Tiina Paunio, Timi Toulopoulou, Elvira Bramon, Marta Di Forti, Robin Murray, Mirella Ruggeri, Evangelos Vassos, Sarah Tosato, Muriel Walshe, Tao Li, Catalina Vasilescu, Thomas W Mühleisen, August G Wang, Henrik Ullum, Srdjan Djurovic, Ingrid Melle, Jes Olesen, Lambertus A Kiemeney, Barbara Franke, Chiara Sabatti, Nelson B Freimer, Jeffrey R Gulcher, Unnur Thorsteinsdottir, Augustine Kong, Ole A Andreassen, Roel A Ophoff, Alexander Georgi, Marcella Rietschel, Thomas Werge, Hannes Petursson, David B Goldstein, Markus M Nöthen, Leena Peltonen, David A Collier, David St Clair, Kari Stefansson. Nature 2008
Times Cited: 1220



Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall, Anthony Leotta, Deepa Pai, Ray Zhang, Yoon-Ha Lee, James Hicks, Sarah J Spence, Annette T Lee, Kaija Puura, Terho Lehtimäki, David Ledbetter, Peter K Gregersen, Joel Bregman, James S Sutcliffe, Vaidehi Jobanputra, Wendy Chung, Dorothy Warburton, Mary-Claire King, David Skuse, Daniel H Geschwind, T Conrad Gilliam, Kenny Ye, Michael Wigler. Science 2007
Times Cited: 1766




List of shared articles



Times cited

Genomic Variation, Evolvability, and the Paradox of Mental Illness.
Camillo Thomas Gualtieri. Front Psychiatry 2021
0



De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families.
Jonathan R Belyeu, Harrison Brand, Harold Wang, Xuefang Zhao, Brent S Pedersen, Julie Feusier, Meenal Gupta, Thomas J Nicholas, Joseph Brown, Lisa Baird,[...]. Am J Hum Genet 2021
1

Recurrent 1q21.1 deletion syndrome: report on variable expression, nonpenetrance and review of literature.
Priyanka Upadhyai, Eram Fatima Amiri, Vishal Singh Guleria, Stephanie L Bielas, Katta Mohan Girisha, Anju Shukla. Clin Dysmorphol 2020
1


Analysis of genes within the schizophrenia-linked 22q11.2 deletion identifies interaction of night owl/LZTR1 and NF1 in GABAergic sleep control.
Gianna W Maurer, Alina Malita, Stanislav Nagy, Takashi Koyama, Thomas M Werge, Kenneth A Halberg, Michael J Texada, Kim Rewitz. PLoS Genet 2020
3

Disorders Associated With Diverse, Recurrent Deletions and Duplications at 1q21.1.
Hui Pang, Xiaowei Yu, Young Mi Kim, Xianfu Wang, Jeremy K Jinkins, Jianing Yin, Shibo Li, Hongcang Gu. Front Genet 2020
1

Interactive effects between hemizygous 15q13.3 microdeletion and peripubertal stress on adult behavioral functions.
Sandra Giovanoli, Thomas M Werge, Preben B Mortensen, Michael Didriksen, Urs Meyer. Neuropsychopharmacology 2019
6

The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Priya Krithivasan, Adele Mitrotti, David A Fasel, Ekaterina Batourina, Matthew G Sampson,[...]. Nat Genet 2019
43

Functional Genomics of Epilepsy and Associated Neurodevelopmental Disorders Using Simple Animal Models: From Genes, Molecules to Brain Networks.
Richard Rosch, Dominic R W Burrows, Laura B Jones, Colin H Peters, Peter Ruben, Éric Samarut. Front Cell Neurosci 2019
3


A genome-wide characterization of copy number variations in native populations of Peninsular Malaysia.
Ruiqing Fu, Siti Shuhada Mokhtar, Maude Elvira Phipps, Boon-Peng Hoh, Shuhua Xu. Eur J Hum Genet 2018
4

Impacts of variants of uncertain significance on parental perceptions of children after prenatal chromosome microarray testing.
Preeya Desai, Hannah Haber, Jessica Bulafka, Amita Russell, Rebecca Clifton, Julia Zachary, Seonjoo Lee, Tianshu Feng, Ronald Wapner, Catherine Monk,[...]. Prenat Diagn 2018
15