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:
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome
Roser Ufartes, Hanna Berger, Katharina Till, et al.
Human Genetics (2020) Vol. 139, Iss. 11, pp. 1363-1379
Open Access | Times Cited: 15
Roser Ufartes, Hanna Berger, Katharina Till, et al.
Human Genetics (2020) Vol. 139, Iss. 11, pp. 1363-1379
Open Access | Times Cited: 15
Showing 15 citing articles:
AUTS2 Syndrome: Molecular Mechanisms and Model Systems
Alecia Biel, Anthony S. Castanza, Ryan Rutherford, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 33
Alecia Biel, Anthony S. Castanza, Ryan Rutherford, et al.
Frontiers in Molecular Neuroscience (2022) Vol. 15
Open Access | Times Cited: 33
The H2A.Z and NuRD associated protein HMG20A controls early head and heart developmental transcription programs
Andreas Herchenröther, Stefanie Gossen, Tobias Friedrich, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 17
Andreas Herchenröther, Stefanie Gossen, Tobias Friedrich, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 17
NRF1 association with AUTS2-Polycomb mediates specific gene activation in the brain
Sanxiong Liu, Kimberly A. Aldinger, Chi Vicky Cheng, et al.
Molecular Cell (2021) Vol. 81, Iss. 22, pp. 4663-4676.e8
Open Access | Times Cited: 37
Sanxiong Liu, Kimberly A. Aldinger, Chi Vicky Cheng, et al.
Molecular Cell (2021) Vol. 81, Iss. 22, pp. 4663-4676.e8
Open Access | Times Cited: 37
Polycomb-dependent histone H2A ubiquitination links developmental disorders with cancer
Simone Tamburri, Eric Conway, Diego Pasini
Trends in Genetics (2021) Vol. 38, Iss. 4, pp. 333-352
Closed Access | Times Cited: 36
Simone Tamburri, Eric Conway, Diego Pasini
Trends in Genetics (2021) Vol. 38, Iss. 4, pp. 333-352
Closed Access | Times Cited: 36
Multidimensional mechanisms of anxiety and depression in Parkinson’s Disease: integrating neuroimaging, neurocircuits, and molecular pathways
Jihu Zhao, Huafang Jia, Pengju Ma, et al.
Pharmacological Research (2025), pp. 107717-107717
Open Access
Jihu Zhao, Huafang Jia, Pengju Ma, et al.
Pharmacological Research (2025), pp. 107717-107717
Open Access
Fbrsl1 is required for heart development in Xenopus laevis and de novo variants in FBRSL1 can cause human heart defects
Hanna Berger, Sarah Gerstner, Marc-Frederik Horstmann, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 3
Hanna Berger, Sarah Gerstner, Marc-Frederik Horstmann, et al.
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access | Times Cited: 3
De Novo Pathogenic Variant in FBRSL1, Non OMIM Gene Paralogue AUTS2, Causes a Novel Recognizable Syndromic Manifestation with Intellectual Disability; An Additional Patient and Review of the Literature
Nenad Bukvić, Marta De Rinaldis, Massimiliano Chetta, et al.
Genes (2024) Vol. 15, Iss. 7, pp. 826-826
Open Access | Times Cited: 1
Nenad Bukvić, Marta De Rinaldis, Massimiliano Chetta, et al.
Genes (2024) Vol. 15, Iss. 7, pp. 826-826
Open Access | Times Cited: 1
Comparing a Novel Malformation Syndrome Caused by Pathogenic Variants in FBRSL1 to AUTS2 Syndrome
Silke Pauli, Hanna Berger, Roser Ufartes, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 6
Silke Pauli, Hanna Berger, Roser Ufartes, et al.
Frontiers in Cell and Developmental Biology (2021) Vol. 9
Open Access | Times Cited: 6
Elizabeth E. Palmer, Chloe Whitton, Mais Hashem, et al.
Clinical Genetics (2021) Vol. 100, Iss. 4, pp. 468-477
Closed Access | Times Cited: 5
CHARGE syndrome and related disorders: a mechanistic link
Roser Ufartes, Regina Grün, Gabriela Salinas, et al.
Human Molecular Genetics (2021) Vol. 30, Iss. 23, pp. 2215-2224
Open Access | Times Cited: 5
Roser Ufartes, Regina Grün, Gabriela Salinas, et al.
Human Molecular Genetics (2021) Vol. 30, Iss. 23, pp. 2215-2224
Open Access | Times Cited: 5
First person – Hanna Berger and Sarah Gerstner
Hanna Berger, Sarah Gerstner
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access
Hanna Berger, Sarah Gerstner
Disease Models & Mechanisms (2024) Vol. 17, Iss. 6
Open Access
The H2A.Z.1/PWWP2A/NuRD-associated protein HMG20A controls early head and heart developmental transcription programs
Andreas Herchenröther, Stefanie Gossen, Tobias Friedrich, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 2
Andreas Herchenröther, Stefanie Gossen, Tobias Friedrich, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 2
NRF1 Association with AUTS2-Polycomb Mediates Specific Gene Activation in the Brain
Sanxiong Liu, Kimberly A. Aldinger, Chi Vicky Cheng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
Sanxiong Liu, Kimberly A. Aldinger, Chi Vicky Cheng, et al.
bioRxiv (Cold Spring Harbor Laboratory) (2021)
Open Access | Times Cited: 1
