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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:

denovo-db: a compendium of humande novovariants
Tychele N. Turner, Yi Qian, Niklas Krumm, et al.
Nucleic Acids Research (2016) Vol. 45, Iss. D1, pp. D804-D811
Open Access | Times Cited: 192

Showing 1-25 of 192 citing articles:

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
Naomi R. Wray, Stephan Ripke, Manuel Mattheisen, et al.
Nature Genetics (2018) Vol. 50, Iss. 5, pp. 668-681
Open Access | Times Cited: 2824
Comparative genetic architectures of schizophrenia in East Asian and European populations
Max Lam, Chia‐Yen Chen, Zhiqiang Li, et al.
Nature Genetics (2019) Vol. 51, Iss. 12, pp. 1670-1678
Open Access | Times Cited: 584
Pharmacogenomics of GPCR Drug Targets
Alexander S. Hauser, Sreenivas Chavali, Ikuo Masuho, et al.
Cell (2017) Vol. 172, Iss. 1-2, pp. 41-54.e19
Open Access | Times Cited: 568
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Holly A.F. Stessman, Bo Xiong, Bradley P. Coe, et al.
Nature Genetics (2017) Vol. 49, Iss. 4, pp. 515-526
Open Access | Times Cited: 513
Dendritic structural plasticity and neuropsychiatric disease
Marc P. Forrest, Euan Parnell, Peter Penzes
Nature reviews. Neuroscience (2018) Vol. 19, Iss. 4, pp. 215-234
Open Access | Times Cited: 424
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity
Bradley P. Coe, Holly A.F. Stessman, Arvis Sulovari, et al.
Nature Genetics (2018) Vol. 51, Iss. 1, pp. 106-116
Open Access | Times Cited: 287
Transcriptome and epigenome landscape of human cortical development modeled in organoids
Anahita Amiri, Gianfilippo Coppola, Soraya Scuderi, et al.
Science (2018) Vol. 362, Iss. 6420
Open Access | Times Cited: 277
Genetic Control of Expression and Splicing in Developing Human Brain Informs Disease Mechanisms
Rebecca L. Walker, Gokul Ramaswami, Christopher Hartl, et al.
Cell (2019) Vol. 179, Iss. 3, pp. 750-771.e22
Open Access | Times Cited: 243
Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders
Víctor Faúndes, William G. Newman, Laura Bernardini, et al.
The American Journal of Human Genetics (2017) Vol. 102, Iss. 1, pp. 175-187
Open Access | Times Cited: 235
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: 166
RMVar: an updated database of functional variants involved in RNA modifications
Xiaotong Luo, Huiqin Li, Jiaqi Liang, et al.
Nucleic Acids Research (2020) Vol. 49, Iss. D1, pp. D1405-D1412
Open Access | Times Cited: 147
Improved pathogenicity prediction for rare human missense variants
Yingzhou Wu, Hanqing Liu, Roujia Li, et al.
The American Journal of Human Genetics (2021) Vol. 108, Iss. 10, pp. 1891-1906
Open Access | Times Cited: 116
POSTAR3: an updated platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins
Weihao Zhao, Shang Zhang, Yumin Zhu, et al.
Nucleic Acids Research (2021) Vol. 50, Iss. D1, pp. D287-D294
Open Access | Times Cited: 113
A cross-species proteomic map reveals neoteny of human synapse development
Li Wang, Kaifang Pang, Li Zhou, et al.
Nature (2023) Vol. 622, Iss. 7981, pp. 112-119
Open Access | Times Cited: 46
Hotspots of missense mutation identify neurodevelopmental disorder genes and functional domains
Madeleine R. Geisheker, Gabriel Heymann, Tianyun Wang, et al.
Nature Neuroscience (2017) Vol. 20, Iss. 8, pp. 1043-1051
Open Access | Times Cited: 165
POSTAR: a platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins
Boqin Hu, Yucheng Yang, Yiming Huang, et al.
Nucleic Acids Research (2016) Vol. 45, Iss. D1, pp. D104-D114
Open Access | Times Cited: 162
VarCards: an integrated genetic and clinical database for coding variants in the human genome
Jinchen Li, Leisheng Shi, Kun Zhang, et al.
Nucleic Acids Research (2017) Vol. 46, Iss. D1, pp. D1039-D1048
Open Access | Times Cited: 162
Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications
Amy B. Wilfert, Arvis Sulovari, Tychele N. Turner, et al.
Genome Medicine (2017) Vol. 9, Iss. 1
Open Access | Times Cited: 131
Sex-Based Analysis of De Novo Variants in Neurodevelopmental Disorders
Tychele N. Turner, Amy B. Wilfert, Trygve E. Bakken, et al.
The American Journal of Human Genetics (2019) Vol. 105, Iss. 6, pp. 1274-1285
Open Access | Times Cited: 125
A Global Map of G Protein Signaling Regulation by RGS Proteins
Ikuo Masuho, Balaji Santhanam, Brian S. Muntean, et al.
Cell (2020) Vol. 183, Iss. 2, pp. 503-521.e19
Open Access | Times Cited: 119
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes
Hui Guo, Michael H. Duyzend, Bradley P. Coe, et al.
Genetics in Medicine (2018) Vol. 21, Iss. 7, pp. 1611-1620
Open Access | Times Cited: 115
DOMINO: Using Machine Learning to Predict Genes Associated with Dominant Disorders
Mathieu Quinodoz, Béryl Royer‐Bertrand, Katarina Cisarova, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 4, pp. 623-629
Open Access | Times Cited: 113
Recapitulation and Reversal of Schizophrenia-Related Phenotypes in Setd1a-Deficient Mice
Jun Mukai, Enrico Cannavò, Gregg W. Crabtree, et al.
Neuron (2019) Vol. 104, Iss. 3, pp. 471-487.e12
Open Access | Times Cited: 113
Spatial Clustering of de Novo Missense Mutations Identifies Candidate Neurodevelopmental Disorder-Associated Genes
Stefan H. Lelieveld, Laurens Wiel, Hanka Venselaar, et al.
The American Journal of Human Genetics (2017) Vol. 101, Iss. 3, pp. 478-484
Open Access | Times Cited: 103
Human and mouse essentiality screens as a resource for disease gene discovery
Pilar Cacheiro, Violeta Muñoz‐Fuentes, Stephen A. Murray, et al.
Nature Communications (2020) Vol. 11, Iss. 1
Open Access | Times Cited: 90
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