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OpenAlex Citation Counts

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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:

Integrating healthcare and research genetic data empowers the discovery of 28 novel developmental disorders
Joanna Kaplanis, Kaitlin E. Samocha, Laurens Wiel, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Open Access | Times Cited: 43

Showing 1-25 of 43 citing articles:

Mapping genomic loci prioritises genes and implicates synaptic biology in schizophrenia
Stephan Ripke, James Walters, Michael O’Donovan
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 317
Single-cell epigenomics reveals mechanisms of human cortical development
Ryan Ziffra, Chang N. Kim, Jayden M. Ross, et al.
Nature (2021) Vol. 598, Iss. 7879, pp. 205-213
Open Access | Times Cited: 219
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
Tianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 165
Exome sequencing identifies rare coding variants in 10 genes which confer substantial risk for schizophrenia
Tarjinder Singh, Benjamin M. Neale, Mark J. Daly
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 138
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
Birte Zurek, Kornelia Ellwanger, Lisenka E.L.M. Vissers, et al.
European Journal of Human Genetics (2021) Vol. 29, Iss. 9, pp. 1325-1331
Open Access | Times Cited: 81
Genetic architecture of autism spectrum disorder: Lessons from large-scale genomic studies
Leejee Choi, Joon‐Yong An
Neuroscience & Biobehavioral Reviews (2021) Vol. 128, pp. 244-257
Open Access | Times Cited: 48
Sensitive spatial genome wide expression profiling at cellular resolution
Robert R. Stickels, Evan Murray, Pawan Kumar, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 44
De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental Delay
Lisenka E.L.M. Vissers, Sreehari Kalvakuri, Elke de Boer, et al.
The American Journal of Human Genetics (2020) Vol. 107, Iss. 1, pp. 164-172
Open Access | Times Cited: 41
Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse brain
Lindsay Liang, Siavash Fazel Darbandi, Sirisha Pochareddy, et al.
Genome Medicine (2021) Vol. 13, Iss. 1
Open Access | Times Cited: 36
New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders
Mariana Moysés‐Oliveira, Rachita Yadav, Serkan Erdin, et al.
Current Opinion in Genetics & Development (2020) Vol. 65, pp. 195-206
Closed Access | Times Cited: 38
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
PLoS Genetics (2021) Vol. 17, Iss. 7, pp. e1009679-e1009679
Open Access | Times Cited: 31
Systematic analysis of exonic germline and postzygotic de novo mutations in bipolar disorder
M. Nishioka, An‐a Kazuno, Takumi Nakamura, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 27
Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia
Jia Wen, Brett Trost, Worrawat Engchuan, et al.
Molecular Psychiatry (2022) Vol. 28, Iss. 1, pp. 475-482
Open Access | Times Cited: 20
Single cell epigenomic atlas of the developing human brain and organoids
Ryan Ziffra, Chang N. Kim, Amy B. Wilfert, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2019)
Closed Access | Times Cited: 34
Human disease genes website series: An international, open and dynamic library for up‐to‐date clinical information
Alexander J.M. Dingemans, Diante E. Stremmelaar, Lisenka E.L.M. Vissers, et al.
American Journal of Medical Genetics Part A (2021) Vol. 185, Iss. 4, pp. 1039-1046
Open Access | Times Cited: 20
Over-representation of potential SP4 target genes within schizophrenia-risk genes
Xianjin Zhou
Molecular Psychiatry (2021) Vol. 27, Iss. 2, pp. 849-854
Open Access | Times Cited: 16
de novo variant calling identifies cancer mutation signatures in the 1000 Genomes Project
Jeffrey K. Ng, Pankaj Vats, Elyn Fritz‐Waters, et al.
Human Mutation (2022) Vol. 43, Iss. 12, pp. 1979-1993
Open Access | Times Cited: 12
Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons
Catarina M. Seabra, Tatsiana Aneichyk, Serkan Erdin, et al.
Molecular Autism (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 16
Mutations in genes encoding regulators of mRNA decapping and translation initiation: links to intellectual disability
Dominique Weil, Amélie Piton, Davor Lessel, et al.
Biochemical Society Transactions (2020) Vol. 48, Iss. 3, pp. 1199-1211
Open Access | Times Cited: 12
Regulatory landscape in brain development and disease
Keeley Spiess, Hyejung Won
Current Opinion in Genetics & Development (2020) Vol. 65, pp. 53-60
Open Access | Times Cited: 9
Reduced reproductive success is associated with selective constraint on human genes
Eugene J. Gardner, Matthew D. C. Neville, Kaitlin E. Samocha, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 7
Dissecting Autism Genetic Risk Using Single-cell RNA-seq Data
Siying Chen, Xueya Zhou, Eve Byington, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 6
de novo variant calling identifies cancer mutation profiles in the 1000 Genomes Project
Jeffrey K. Ng, Pankaj Vats, Elyn Fritz‐Waters, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 6
De novo missense variants in LMBRD2 are associated with developmental and motor delays, brain structure abnormalities and dysmorphic features
Alka Malhotra, Alban Ziegler, Li Shu, et al.
Journal of Medical Genetics (2020) Vol. 58, Iss. 10, pp. 712-716
Closed Access | Times Cited: 5
Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
Enrique Audain, Anna Wilsdon, Jeroen Breckpot, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 4
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