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:
Recurrent de novo missense variants in GNB2 can cause syndromic intellectual disability
Natalie B. Tan, Alistair T. Pagnamenta, Matteo P. Ferla, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 5, pp. 511-516
Open Access | Times Cited: 8
Natalie B. Tan, Alistair T. Pagnamenta, Matteo P. Ferla, et al.
Journal of Medical Genetics (2021) Vol. 59, Iss. 5, pp. 511-516
Open Access | Times Cited: 8
Showing 8 citing articles:
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death
Alicia B. Byrne, Peer Arts, Thuong Ha, et al.
Nature Medicine (2023) Vol. 29, Iss. 1, pp. 180-189
Open Access | Times Cited: 34
Alicia B. Byrne, Peer Arts, Thuong Ha, et al.
Nature Medicine (2023) Vol. 29, Iss. 1, pp. 180-189
Open Access | Times Cited: 34
Venus: Elucidating the Impact of Amino Acid Variants on Protein Function Beyond Structure Destabilisation
Matteo P. Ferla, Alistair T. Pagnamenta, Leonidas Koukouflis, et al.
Journal of Molecular Biology (2022) Vol. 434, Iss. 11, pp. 167567-167567
Open Access | Times Cited: 16
Matteo P. Ferla, Alistair T. Pagnamenta, Leonidas Koukouflis, et al.
Journal of Molecular Biology (2022) Vol. 434, Iss. 11, pp. 167567-167567
Open Access | Times Cited: 16
Review of childhood genetic nephrolithiasis and nephrocalcinosis
Ashley M. Gefen, Joshua J. Zaritsky
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 3
Ashley M. Gefen, Joshua J. Zaritsky
Frontiers in Genetics (2024) Vol. 15
Open Access | Times Cited: 3
An Update of G-Protein-Coupled Receptor Signaling and Its Deregulation in Gastric Carcinogenesis
Huan Yan, Jingling Zhang, Kam Tong Leung, et al.
Cancers (2023) Vol. 15, Iss. 3, pp. 736-736
Open Access | Times Cited: 4
Huan Yan, Jingling Zhang, Kam Tong Leung, et al.
Cancers (2023) Vol. 15, Iss. 3, pp. 736-736
Open Access | Times Cited: 4
Prenatal exome sequencing, a powerful tool for improving the description of prenatal features associated with genetic disorders
Christel Thauvin‐Robinet, Aurore Garde, Julian Delanne, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 10, pp. 1179-1197
Open Access | Times Cited: 1
Christel Thauvin‐Robinet, Aurore Garde, Julian Delanne, et al.
Prenatal Diagnosis (2024) Vol. 44, Iss. 10, pp. 1179-1197
Open Access | Times Cited: 1
Genomic autopsy offers answers for pregnancy loss and perinatal death
Nature Medicine (2023) Vol. 29, Iss. 1, pp. 41-42
Closed Access | Times Cited: 1
Nature Medicine (2023) Vol. 29, Iss. 1, pp. 41-42
Closed Access | Times Cited: 1
A national diagnostic framework for patients with ultra-rare disorders: molecular genetic findings using phenotypic and sequencing data
Peter Krawitz
Research Square (Research Square) (2022)
Open Access | Times Cited: 2
Peter Krawitz
Research Square (Research Square) (2022)
Open Access | Times Cited: 2
A genomic autopsy identifies causes of perinatal death and provides options to prevent recurrence
Hamish S. Scott, Alicia B. Byrne, Peer Arts, et al.
Research Square (Research Square) (2022)
Open Access
Hamish S. Scott, Alicia B. Byrne, Peer Arts, et al.
Research Square (Research Square) (2022)
Open Access
