A citation-based method for searching scientific literature

George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll, Michael C O'Donovan, Michael J Owen. Biol Psychiatry 2014
Times Cited: 190



Evangelos Vassos, David A Collier, Simon Holden, Christine Patch, Dan Rujescu, David St Clair, Cathryn M Lewis. Hum Mol Genet 2010
Times Cited: 104




List of shared articles



Times cited

Polygenic burden has broader impact on health, cognition, and socioeconomic outcomes than most rare and high-risk copy number variants.
Elmo Christian Saarentaus, Aki Samuli Havulinna, Nina Mars, Ari Ahola-Olli, Tuomo Tapio Johannes Kiiskinen, Juulia Partanen, Sanni Ruotsalainen, Mitja Kurki, Lea Martta Urpa, Lei Chen,[...]. Mol Psychiatry 2021
0

Genetic architecture of schizophrenia: a review of major advancements.
Sophie E Legge, Marcos L Santoro, Sathish Periyasamy, Adeniran Okewole, Arsalan Arsalan, Kaarina Kowalec. Psychol Med 2021
1

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

Clinical characterization of individuals with the distal 1q21.1 microdeletion.
Stacey D Edwards, Katharina V Schulze, Jill A Rosenfeld, Lauren E Westerfield, Amanda Gerard, Bo Yuan, Elena L Grigorenko, Jennifer E Posey, Weimin Bi, Pengfei Liu. Am J Med Genet A 2021
0

16p11 Duplication Disrupts Hippocampal-Orbitofrontal-Amygdala Connectivity, Revealing a Neural Circuit Endophenotype for Schizophrenia.
Greg C Bristow, David M Thomson, Rebecca L Openshaw, Emma J Mitchell, Judith A Pratt, Neil Dawson, Brian J Morris. Cell Rep 2020
6

Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study.
Johan H Thygesen, Amelia Presman, Jasmine Harju-Seppänen, Haritz Irizar, Rebecca Jones, Karoline Kuchenbaecker, Kuang Lin, Behrooz Z Alizadeh, Isabelle Austin-Zimmerman, Agna Bartels-Velthuis,[...]. Mol Psychiatry 2020
2

NRXN1 deletion syndrome; phenotypic and penetrance data from 34 families.
Maryam Al Shehhi, Eva B Forman, Jacqueline E Fitzgerald, Veronica McInerney, Janusz Krawczyk, Sanbing Shen, David R Betts, Linda Mc Ardle, Kathleen M Gorman, Mary D King,[...]. Eur J Med Genet 2019
22

Integrating Genomics into Psychiatric Practice: Ethical and Legal Challenges for Clinicians.
Eric T Ward, Kristin M Kostick, Gabriel Lázaro-Muñoz. Harv Rev Psychiatry 2019
3

Copy Number Variation of Satellite III (1q12) in Patients With Schizophrenia.
Elizaveta S Ershova, Oksana N Agafonova, Natalia V Zakharova, Lidia V Bravve, Elizaveta M Jestkova, Vera E Golimbet, Tatiana V Lezheiko, Anna Y Morozova, Andrey V Martynov, Roman V Veiko,[...]. Front Genet 2019
2

Improved ethical guidance for the return of results from psychiatric genomics research.
G Lázaro-Muñoz, M S Farrell, J J Crowley, D M Filmyer, R A Shaughnessy, R C Josiassen, P F Sullivan. Mol Psychiatry 2018
19