A citation-based method for searching scientific literature

Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer, Noa Carrera, Isla Humphreys, Jessica S Johnson, Panos Roussos, Douglas D Barker, Eric Banks, Vihra Milanova, Seth G Grant, Eilis Hannon, Samuel A Rose, Kimberly Chambert, Milind Mahajan, Edward M Scolnick, Jennifer L Moran, George Kirov, Aarno Palotie, Steven A McCarroll, Peter Holmans, Pamela Sklar, Michael J Owen, Shaun M Purcell, Michael C O'Donovan. Nature 2014
Times Cited: 955



Stefan H Lelieveld, Margot R F Reijnders, Rolph Pfundt, Helger G Yntema, Erik-Jan Kamsteeg, Petra de Vries, Bert B A de Vries, Marjolein H Willemsen, Tjitske Kleefstra, Katharina Löhner, Maaike Vreeburg, Servi J C Stevens, Ineke van der Burgt, Ernie M H F Bongers, Alexander P A Stegmann, Patrick Rump, Tuula Rinne, Marcel R Nelen, Joris A Veltman, Lisenka E L M Vissers, Han G Brunner, Christian Gilissen. Nat Neurosci 2016
Times Cited: 219




List of shared articles



Times cited

A novel stop-gain CUL3 mutation in a Japanese patient with autism spectrum disorder.
Sota Iwafuchi, Atsuo Kikuchi, Wakaba Endo, Takehiko Inui, Yu Aihara, Kazuhito Satou, Tadashi Kaname, Shigeo Kure. Brain Dev 2021
0

Exploring the biological role of postzygotic and germinal de novo mutations in ASD.
A Alonso-Gonzalez, M Calaza, J Amigo, J González-Peñas, R Martínez-Regueiro, M Fernández-Prieto, M Parellada, C Arango, Cristina Rodriguez-Fontenla, A Carracedo. Sci Rep 2021
0

Cross-Disorder Analysis of De Novo Variants Increases the Power of Prioritising Candidate Genes.
Kuokuo Li, Zhengbao Ling, Tengfei Luo, Guihu Zhao, Qiao Zhou, Xiaomeng Wang, Kun Xia, Jinchen Li, Bin Li. Life (Basel) 2021
0

Targeted sequencing and integrative analysis to prioritize candidate genes in neurodevelopmental disorders.
Yi Zhang, Tao Wang, Yan Wang, Kun Xia, Jinchen Li, Zhongsheng Sun. Mol Neurobiol 2021
0

Family-Based Genome-Wide Association Study of Autism Spectrum Disorder in Middle Eastern Families.
Yasser Al-Sarraj, Eman Al-Dous, Rowaida Z Taha, Dina Ahram, Fouad Alshaban, Mohammed Tolfat, Hatem El-Shanti, Omar M E Albagha. Genes (Basel) 2021
0

Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder.
Masaki Nishioka, An-A Kazuno, Takumi Nakamura, Naomi Sakai, Takashi Hayama, Kumiko Fujii, Koji Matsuo, Atsuko Komori, Mizuho Ishiwata, Yoshinori Watanabe,[...]. Nat Commun 2021
0

JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome.
Eline A Verberne, Shuxiang Goh, Jade England, Manon van Ginkel, Louise Rafael-Croes, Saskia Maas, Abeltje Polstra, Yuri A Zarate, Katherine A Bosanko, Kieran B Pechter,[...]. Genet Med 2021
0

De novo mutations in folate-related genes associated with common developmental disorders.
Tengfei Luo, Kuokuo Li, Zhengbao Ling, Guihu Zhao, Bin Li, Zheng Wang, Xiaomeng Wang, Ying Han, Lu Xia, Yi Zhang,[...]. Comput Struct Biotechnol J 2021
0

Cross-Disorder Analysis of De Novo Mutations in Neuropsychiatric Disorders.
Kuokuo Li, Zhenghuan Fang, Guihu Zhao, Bin Li, Chao Chen, Lu Xia, Lin Wang, Tengfei Luo, Xiaomeng Wang, Zheng Wang,[...]. J Autism Dev Disord 2021
0

Gene4Denovo: an integrated database and analytic platform for de novo mutations in humans.
Guihu Zhao, Kuokuo Li, Bin Li, Zheng Wang, Zhenghuan Fang, Xiaomeng Wang, Yi Zhang, Tengfei Luo, Qiao Zhou, Lin Wang,[...]. Nucleic Acids Res 2020
16

Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.
Daniel P Howrigan, Samuel A Rose, Kaitlin E Samocha, Menachem Fromer, Felecia Cerrato, Wei J Chen, Claire Churchhouse, Kimberly Chambert, Sharon D Chandler, Mark J Daly,[...]. Nat Neurosci 2020
31