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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 26-50 of 43 citing articles:

Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations
Elliott Rees, Hugo Creeth, Hai‐Gwo Hwu, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 4
Refinement of the clinical variant interpretation framework by statistical evidence and machine learning
Atsushi Takata, Kohei Hamanaka, Naomichi Matsumoto
Med (2021) Vol. 2, Iss. 5, pp. 611-632.e9
Open Access | Times Cited: 4
Interaction studies of risk proteins in human induced neurons reveal convergent biology and novel mechanisms underlying autism spectrum disorders
Greta Pintacuda, Yu-Han H. Hsu, Kalliopi Tsafou, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 4
Neurogenomics with Application to Schizophrenia and Other Major Neuropsychiatric Diseases with Complex Heredity
Laurence Melnick
(2024), pp. 117-143
Closed Access
Exploring 15q13.3 copy number variants in iPSCs
Madelyn A. Gillentine
Elsevier eBooks (2022), pp. 333-360
Closed Access | Times Cited: 2
The contribution of X-linked coding variation to severe developmental disorders
Hilary C. Martin, Eugene J. Gardner, Kaitlin E. Samocha, et al.
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 2
Neurotrophin receptor activation rescues cognitive and synaptic abnormalities caused by mutation of the psychiatric risk geneCacna1c
Cezar M. Tigaret, Tzu‐Ching E. Lin, Edward Morrell, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 2
De NovoMutation in an Enhancer ofEBF3in simplex autism
Evin M. Padhi, Tristan J. Hayeck, Brandon J. Mannion, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 2
Schizophrenia, autism spectrum disorders and developmental disorders share specific disruptive coding mutations
Elliott Rees, Hugo Creeth, Hai‐Gwo Hwu, et al.
Research Square (Research Square) (2020)
Open Access | Times Cited: 2
Prevalence of Returnable Genetic Results Based on Recognizable Phenotypes among Children with Autism Spectrum Disorder
Somer Bishop, Audrey Thurm, Elise Robinson, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 2
Variants inPRKAR1Bcause a neurodevelopmental disorder with autism spectrum disorder,apraxia, and insensitivity to pain
Felix Marbach, Georgi Stoyanov, Florian Erger, et al.
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access | Times Cited: 1
AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders
Johann Lieberwirth, Benjamin Büttner, Chiara Klöckner, et al.
Authorea (Authorea) (2022)
Open Access | Times Cited: 1
A rare missense variant in theATP2C2gene is associated with language impairment and related measures
Angela Martinelli, Mabel L. Rice, Joel B. Talcott, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
Using brain cell-type-specific protein interactomes to interpret genetic data in schizophrenia
Yu-Han H. Hsu, Eugeniu Nacu, Ruize Liu, et al.
medRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
Over-Representation of Potential SP4 Target Genes within Schizophrenia-Risk Genes
Xianjin Zhou
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
Detecting cryptic clinically-relevant structural variation in exome sequencing data increases diagnostic yield for developmental disorders
Eugene J. Gardner, Alejandro Sifrim, Sarah Lindsay, et al.
medRxiv (Cold Spring Harbor Laboratory) (2020)
Open Access
AutoCaSc: Prioritizing candidate genes for neurodevelopmental disorders
Bernt Popp, Johann Lieberwirth, Benjamin Büttner, et al.
Authorea (Authorea) (2022)
Open Access
Integration of Functional Genomic Data in Genetic Analysis
Siying Chen
(2021)
Closed Access
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