OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!
If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.
Requested Article:
Neuron-specific signatures in the chromosomal connectome associated with schizophrenia risk
Prashanth Rajarajan, Tyler Borrman, Will Liao, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 199
Prashanth Rajarajan, Tyler Borrman, Will Liao, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 199
Showing 1-25 of 199 citing articles:
Single-cell epigenomic analyses implicate candidate causal variants at inherited risk loci for Alzheimer’s and Parkinson’s diseases
M. Ryan Corces, Anna Shcherbina, Soumya Kundu, et al.
Nature Genetics (2020) Vol. 52, Iss. 11, pp. 1158-1168
Open Access | Times Cited: 290
M. Ryan Corces, Anna Shcherbina, Soumya Kundu, et al.
Nature Genetics (2020) Vol. 52, Iss. 11, pp. 1158-1168
Open Access | Times Cited: 290
A computational tool (H-MAGMA) for improved prediction of brain-disorder risk genes by incorporating brain chromatin interaction profiles
Nancy Y. A. Sey, Benxia Hu, Won Mah, et al.
Nature Neuroscience (2020) Vol. 23, Iss. 4, pp. 583-593
Open Access | Times Cited: 260
Nancy Y. A. Sey, Benxia Hu, Won Mah, et al.
Nature Neuroscience (2020) Vol. 23, Iss. 4, pp. 583-593
Open Access | Times Cited: 260
Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction
Richard Karlsson Linnér, Travis T. Mallard, Peter B. Barr, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 10, pp. 1367-1376
Open Access | Times Cited: 238
Richard Karlsson Linnér, Travis T. Mallard, Peter B. Barr, et al.
Nature Neuroscience (2021) Vol. 24, Iss. 10, pp. 1367-1376
Open Access | Times Cited: 238
Mapping cis-regulatory chromatin contacts in neural cells links neuropsychiatric disorder risk variants to target genes
Michael Song, Xiaoyu Yang, Xingjie Ren, et al.
Nature Genetics (2019) Vol. 51, Iss. 8, pp. 1252-1262
Open Access | Times Cited: 169
Michael Song, Xiaoyu Yang, Xingjie Ren, et al.
Nature Genetics (2019) Vol. 51, Iss. 8, pp. 1252-1262
Open Access | Times Cited: 169
Changes in genome architecture and transcriptional dynamics progress independently of sensory experience during post-natal brain development
Longzhi Tan, Wenping Ma, Honggui Wu, et al.
Cell (2021) Vol. 184, Iss. 3, pp. 741-758.e17
Open Access | Times Cited: 157
Longzhi Tan, Wenping Ma, Honggui Wu, et al.
Cell (2021) Vol. 184, Iss. 3, pp. 741-758.e17
Open Access | Times Cited: 157
Robust Hi-C Maps of Enhancer-Promoter Interactions Reveal the Function of Non-coding Genome in Neural Development and Diseases
Leina Lu, Xiaoxiao Liu, Wei‐Kai Huang, et al.
Molecular Cell (2020) Vol. 79, Iss. 3, pp. 521-534.e15
Open Access | Times Cited: 139
Leina Lu, Xiaoxiao Liu, Wei‐Kai Huang, et al.
Molecular Cell (2020) Vol. 79, Iss. 3, pp. 521-534.e15
Open Access | Times Cited: 139
3D Genome of macaque fetal brain reveals evolutionary innovations during primate corticogenesis
Xin Luo, Yuting Liu, Dachang Dang, et al.
Cell (2021) Vol. 184, Iss. 3, pp. 723-740.e21
Open Access | Times Cited: 109
Xin Luo, Yuting Liu, Dachang Dang, et al.
Cell (2021) Vol. 184, Iss. 3, pp. 723-740.e21
Open Access | Times Cited: 109
Neuronal DNA double-strand breaks lead to genome structural variations and 3D genome disruption in neurodegeneration
Vishnu Dileep, Carles A. Boix, Hansruedi Mathys, et al.
Cell (2023) Vol. 186, Iss. 20, pp. 4404-4421.e20
Open Access | Times Cited: 62
Vishnu Dileep, Carles A. Boix, Hansruedi Mathys, et al.
Cell (2023) Vol. 186, Iss. 20, pp. 4404-4421.e20
Open Access | Times Cited: 62
The schizophrenia syndrome, circa 2024: What we know and how that informs its nature
Rajiv Tandon, Henry A. Nasrallah, Schahram Akbarian, et al.
Schizophrenia Research (2023) Vol. 264, pp. 1-28
Open Access | Times Cited: 57
Rajiv Tandon, Henry A. Nasrallah, Schahram Akbarian, et al.
Schizophrenia Research (2023) Vol. 264, pp. 1-28
Open Access | Times Cited: 57
Molecular cascades and cell type–specific signatures in ASD revealed by single-cell genomics
Brie Wamsley, Lucy Bicks, Yuyan Cheng, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 29
Brie Wamsley, Lucy Bicks, Yuyan Cheng, et al.
Science (2024) Vol. 384, Iss. 6698
Open Access | Times Cited: 29
Cell type-specific epigenetic links to schizophrenia risk in the brain
Isabel Mendizabal, Stefano Berto, Noriyoshi Usui, et al.
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 101
Isabel Mendizabal, Stefano Berto, Noriyoshi Usui, et al.
Genome biology (2019) Vol. 20, Iss. 1
Open Access | Times Cited: 101
Synaptic Elimination in Neurological Disorders
Pablo Leal Cardozo, Izabella B. Q. de Lima, Esther M. A. Maciel, et al.
Current Neuropharmacology (2019) Vol. 17, Iss. 11, pp. 1071-1095
Open Access | Times Cited: 96
Pablo Leal Cardozo, Izabella B. Q. de Lima, Esther M. A. Maciel, et al.
Current Neuropharmacology (2019) Vol. 17, Iss. 11, pp. 1071-1095
Open Access | Times Cited: 96
Allele-specific open chromatin in human iPSC neurons elucidates functional disease variants
Siwei Zhang, Hanwen Zhang, Yifan Zhou, et al.
Science (2020) Vol. 369, Iss. 6503, pp. 561-565
Open Access | Times Cited: 96
Siwei Zhang, Hanwen Zhang, Yifan Zhou, et al.
Science (2020) Vol. 369, Iss. 6503, pp. 561-565
Open Access | Times Cited: 96
Massively parallel discovery of human-specific substitutions that alter enhancer activity
Severin Uebbing, Jake Gockley, Steven K. Reilly, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 118, Iss. 2
Open Access | Times Cited: 96
Severin Uebbing, Jake Gockley, Steven K. Reilly, et al.
Proceedings of the National Academy of Sciences (2020) Vol. 118, Iss. 2
Open Access | Times Cited: 96
Neurobiological functions of transcriptional enhancers
Alex S. Nord, Anne E. West
Nature Neuroscience (2019) Vol. 23, Iss. 1, pp. 5-14
Open Access | Times Cited: 87
Alex S. Nord, Anne E. West
Nature Neuroscience (2019) Vol. 23, Iss. 1, pp. 5-14
Open Access | Times Cited: 87
Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders
Benxia Hu, Hyejung Won, Won Mah, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 86
Benxia Hu, Hyejung Won, Won Mah, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 86
Bondita Dehingia, Małgorzata Milewska, Marcin Janowski, et al.
EMBO Reports (2022) Vol. 23, Iss. 9
Open Access | Times Cited: 66
A multi-ancestry genetic study of pain intensity in 598,339 veterans
Sylvanus Toikumo, Rachel Vickers‐Smith, Zeal Jinwala, et al.
Nature Medicine (2024) Vol. 30, Iss. 4, pp. 1075-1084
Open Access | Times Cited: 14
Sylvanus Toikumo, Rachel Vickers‐Smith, Zeal Jinwala, et al.
Nature Medicine (2024) Vol. 30, Iss. 4, pp. 1075-1084
Open Access | Times Cited: 14
Monozygotic twins discordant for schizophrenia differ in maturation and synaptic transmission
Shani Stern, Lei Zhang, Meiyan Wang, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 10, pp. 3208-3222
Open Access | Times Cited: 11
Shani Stern, Lei Zhang, Meiyan Wang, et al.
Molecular Psychiatry (2024) Vol. 29, Iss. 10, pp. 3208-3222
Open Access | Times Cited: 11
Massively parallel disruption of enhancers active in human neural stem cells
Evan Geller, Mark Noble, Matheo Morales, et al.
Cell Reports (2024) Vol. 43, Iss. 2, pp. 113693-113693
Open Access | Times Cited: 10
Evan Geller, Mark Noble, Matheo Morales, et al.
Cell Reports (2024) Vol. 43, Iss. 2, pp. 113693-113693
Open Access | Times Cited: 10
Schizophrenia genomics: genetic complexity and functional insights
Patrick F. Sullivan, Shuyang Yao, Jens Hjerling‐Leffler
Nature reviews. Neuroscience (2024) Vol. 25, Iss. 9, pp. 611-624
Closed Access | Times Cited: 10
Patrick F. Sullivan, Shuyang Yao, Jens Hjerling‐Leffler
Nature reviews. Neuroscience (2024) Vol. 25, Iss. 9, pp. 611-624
Closed Access | Times Cited: 10
SATB2 organizes the 3D genome architecture of cognition in cortical neurons
Nico Wahl, Sergio Espeso‐Gil, Paola Chietera, et al.
Molecular Cell (2024) Vol. 84, Iss. 4, pp. 621-639.e9
Open Access | Times Cited: 8
Nico Wahl, Sergio Espeso‐Gil, Paola Chietera, et al.
Molecular Cell (2024) Vol. 84, Iss. 4, pp. 621-639.e9
Open Access | Times Cited: 8
Research Domain Criteria: Strengths, Weaknesses, and Potential Alternatives for Future Psychiatric Research
Christopher A. Ross, Russell L. Margolis
Complex Psychiatry (2019) Vol. 5, Iss. 4, pp. 218-236
Open Access | Times Cited: 72
Christopher A. Ross, Russell L. Margolis
Complex Psychiatry (2019) Vol. 5, Iss. 4, pp. 218-236
Open Access | Times Cited: 72
The genome-wide risk alleles for psychiatric disorders at 3p21.1 show convergent effects on mRNA expression, cognitive function, and mushroom dendritic spine
Zhihui Yang, Danyang Zhou, Huijuan Li, et al.
Molecular Psychiatry (2019) Vol. 25, Iss. 1, pp. 48-66
Closed Access | Times Cited: 71
Zhihui Yang, Danyang Zhou, Huijuan Li, et al.
Molecular Psychiatry (2019) Vol. 25, Iss. 1, pp. 48-66
Closed Access | Times Cited: 71
Fifty Years of Research on Schizophrenia: The Ascendance of the Glutamatergic Synapse
Joseph T. Coyle, W. Brad Ruzicka, Darrick T. Balu
American Journal of Psychiatry (2020) Vol. 177, Iss. 12, pp. 1119-1128
Open Access | Times Cited: 59
Joseph T. Coyle, W. Brad Ruzicka, Darrick T. Balu
American Journal of Psychiatry (2020) Vol. 177, Iss. 12, pp. 1119-1128
Open Access | Times Cited: 59
