A citation-based method for searching scientific literature

Bin Xu, Iuliana Ionita-Laza, J Louw Roos, Braden Boone, Scarlet Woodrick, Yan Sun, Shawn Levy, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2012
Times Cited: 289



Bin Xu, J Louw Roos, Phillip Dexheimer, Braden Boone, Brooks Plummer, Shawn Levy, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2011
Times Cited: 312




List of shared articles



Times cited

Familial Psychosis Associated With a Missense Mutation at MACF1 Gene Combined With the Rare Duplications DUP3p26.3 and DUP16q23.3, Affecting the CNTN6 and CDH13 Genes.
Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Víctor Asensio, Bernat Ortega-Vila, Diego Marzese, Carme Vidal, Carmen Santos,[...]. Front Genet 2021
0

Targeted sequencing and integrative analysis of 3,195 Chinese patients with neurodevelopmental disorders prioritized 26 novel candidate genes.
Tao Wang, Yi Zhang, Liqui Liu, Yan Wang, Huiqian Chen, Tianda Fan, Jinchen Li, Kun Xia, Zhongsheng Sun. J Genet Genomics 2021
0

Prioritizing de novo autism risk variants with calibrated gene- and variant-scoring models.
Yuxiang Jiang, Jorge Urresti, Kymberleigh A Pagel, Akula Bala Pramod, Lilia M Iakoucheva, Predrag Radivojac. Hum Genet 2021
0

The abiding relevance of mouse models of rare mutations to psychiatric neuroscience and therapeutics.
Joseph A Gogos, Gregg Crabtree, Anastasia Diamantopoulou. Schizophr Res 2020
4

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
33

Novel genetic susceptibility loci identified by family based whole exome sequencing in Han Chinese schizophrenia patients.
Mo Li, Lu Shen, Luan Chen, Cong Huai, Hailiang Huang, Xi Wu, Chao Yang, Jingsong Ma, Wei Zhou, Huihui Du,[...]. Transl Psychiatry 2020
4

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families.
Andreas J Forstner, Sascha B Fischer, Lorena M Schenk, Jana Strohmaier, Anna Maaser-Hecker, Céline S Reinbold, Sugirthan Sivalingam, Julian Hecker, Fabian Streit, Franziska Degenhardt,[...]. Transl Psychiatry 2020
5

SZDB2.0: an updated comprehensive resource for schizophrenia research.
Yong Wu, Xiaoyan Li, Jiewei Liu, Xiong-Jian Luo, Yong-Gang Yao. Hum Genet 2020
7

Genes regulated by BCL11B during T-cell development are enriched for de novo mutations found in schizophrenia patients.
Laura Fahey, Gary Donohoe, Pilib Ó Broin, Derek W Morris. Am J Med Genet B Neuropsychiatr Genet 2020
0

Identification of de novo mutations in prenatal neurodevelopment-associated genes in schizophrenia in two Han Chinese patient-sibling family-based cohorts.
Shan Jiang, Daizhan Zhou, Yin-Ying Wang, Peilin Jia, Chunling Wan, Xingwang Li, Guang He, Dongmei Cao, Xiaoqian Jiang, Kenneth S Kendler,[...]. Transl Psychiatry 2020
1

Inferring the molecular and phenotypic impact of amino acid variants with MutPred2.
Vikas Pejaver, Jorge Urresti, Jose Lugo-Martinez, Kymberleigh A Pagel, Guan Ning Lin, Hyun-Jun Nam, Matthew Mort, David N Cooper, Jonathan Sebat, Lilia M Iakoucheva,[...]. Nat Commun 2020
29

Assessment of de novo copy-number variations in Italian patients with schizophrenia: Detection of putative mutations involving regulatory enhancer elements.
Giulio Piluso, Palmiero Monteleone, Silvana Galderisi, Teresa Giugliano, Alessandro Bertolino, Paola Rocca, Alessandro Rossi, Armida Mucci, Eugenio Aguglia, Ileana Andriola,[...]. World J Biol Psychiatry 2019
6

Candidate CSPG4 mutations and induced pluripotent stem cell modeling implicate oligodendrocyte progenitor cell dysfunction in familial schizophrenia.
Femke M de Vrij, Christian G Bouwkamp, Nilhan Gunhanlar, Guy Shpak, Bas Lendemeijer, Maarouf Baghdadi, Shreekara Gopalakrishna, Mehrnaz Ghazvini, Tracy M Li, Marialuisa Quadri,[...]. Mol Psychiatry 2019
21

Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort Analysis.
Jibin John, Aditya Sharma, Prachi Kukshal, Triptish Bhatia, Vishwajit L Nimgaonkar, Smita N Deshpande, B K Thelma. Schizophr Bull 2019
7


Enrichment of rare genetic variants in astrocyte gene enriched co-expression modules altered in postmortem brain samples of schizophrenia.
Javier González-Peñas, Javier Costas, María José Ginzo Villamayor, Bin Xu. Neurobiol Dis 2019
5

Exome Sequencing Identifies TENM4 as a Novel Candidate Gene for Schizophrenia in the SCZD2 Locus at 11q14-21.
Chao-Biao Xue, Zhou-Heng Xu, Jun Zhu, Yu Wu, Xi-Hang Zhuang, Qu-Liang Chen, Cai-Ru Wu, Jin-Tao Hu, Hou-Shi Zhou, Wei-Hang Xie,[...]. Front Genet 2019
5


Paternal-age-related de novo mutations and risk for five disorders.
Jacob L Taylor, Jean-Christophe P G Debost, Sarah U Morton, Emilie M Wigdor, Henrike O Heyne, Dennis Lal, Daniel P Howrigan, Alex Bloemendal, Janne T Larsen, Jack A Kosmicki,[...]. Nat Commun 2019
21

Temporal dynamics of miRNAs in human DLPFC and its association with miRNA dysregulation in schizophrenia.
Zhonghua Hu, Shouguo Gao, Daniel Lindberg, Debabrata Panja, Yoshi Wakabayashi, Keshen Li, Joel E Kleinman, Jun Zhu, Zheng Li. Transl Psychiatry 2019
9

Recapitulation and Reversal of Schizophrenia-Related Phenotypes in Setd1a-Deficient Mice.
Jun Mukai, Enrico Cannavò, Gregg W Crabtree, Ziyi Sun, Anastasia Diamantopoulou, Pratibha Thakur, Chia-Yuan Chang, Yifei Cai, Stavros Lomvardas, Atsushi Takata,[...]. Neuron 2019
20

Identification of de novo germline mutations and causal genes for sporadic diseases using trio-based whole-exome/genome sequencing.
Zi-Bing Jin, Zhongshan Li, Zhenwei Liu, Yi Jiang, Xue-Bi Cai, Jinyu Wu. Biol Rev Camb Philos Soc 2018
16

A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency.
Sandra Jansen, Alexander Hoischen, Bradley P Coe, Gemma L Carvill, Hilde Van Esch, Daniëlle G M Bosch, Ulla A Andersen, Carl Baker, Marijke Bauters, Raphael A Bernier,[...]. Eur J Hum Genet 2018
15

The Candidate Schizophrenia Risk Gene DGCR2 Regulates Early Steps of Corticogenesis.
Aude Molinard-Chenu, Alexandre Dayer. Biol Psychiatry 2018
10

Dendritic structural plasticity and neuropsychiatric disease.
Marc P Forrest, Euan Parnell, Peter Penzes. Nat Rev Neurosci 2018
146

Recent Advances in the Genetics of Schizophrenia.
Dimitrios Avramopoulos. Mol Neuropsychiatry 2018
34

De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report.
Chrystal F Mavros, Catherine A Brownstein, Roshni Thyagrajan, Casie A Genetti, Sahil Tembulkar, Kelsey Graber, Quinn Murphy, Kristin Cabral, Grace E VanNoy, Matthew Bainbridge,[...]. BMC Med Genet 2018
2

The role of genetics and genomics in clinical psychiatry.
Margret R Hoehe, Deborah J Morris-Rosendahl. Dialogues Clin Neurosci 2018
6

Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes.
M N Loviglio, M Leleu, K Männik, M Passeggeri, G Giannuzzi, I van der Werf, S M Waszak, M Zazhytska, I Roberts-Caldeira, N Gheldof,[...]. Mol Psychiatry 2017
37

Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics.
Ina Giegling, Ladislav Hosak, Rainald Mössner, Alessandro Serretti, Frank Bellivier, Stephan Claes, David A Collier, Alejo Corrales, Lynn E DeLisi, Carla Gallo,[...]. World J Biol Psychiatry 2017
29


Investigation of SHANK3 in schizophrenia.
Ana de Sena Cortabitarte, Franziska Degenhardt, Jana Strohmaier, Maren Lang, Birgit Weiss, Ralph Roeth, Ina Giegling, Stefanie Heilmann-Heimbach, Andrea Hofmann, Dan Rujescu,[...]. Am J Med Genet B Neuropsychiatr Genet 2017
18