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:
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?
Luca Ferrari, Eleonora Mangano, Maria Teresa Bonati, et al.
European Journal of Human Genetics (2020) Vol. 28, Iss. 10, pp. 1432-1445
Open Access | Times Cited: 13
Luca Ferrari, Eleonora Mangano, Maria Teresa Bonati, et al.
European Journal of Human Genetics (2020) Vol. 28, Iss. 10, pp. 1432-1445
Open Access | Times Cited: 13
Showing 13 citing articles:
Machine learning approaches to explore digenic inheritance
Atsuko Okazaki, Jürg Ott
Trends in Genetics (2022) Vol. 38, Iss. 10, pp. 1013-1018
Open Access | Times Cited: 29
Atsuko Okazaki, Jürg Ott
Trends in Genetics (2022) Vol. 38, Iss. 10, pp. 1013-1018
Open Access | Times Cited: 29
Preclinical evaluation of CRISPR-based therapies for Noonan syndrome caused by deep-intronic LZTR1 variants
Carolin Knauer, Henrike Haltern, Eric Schoger, et al.
Molecular Therapy — Nucleic Acids (2024) Vol. 35, Iss. 1, pp. 102123-102123
Open Access | Times Cited: 5
Carolin Knauer, Henrike Haltern, Eric Schoger, et al.
Molecular Therapy — Nucleic Acids (2024) Vol. 35, Iss. 1, pp. 102123-102123
Open Access | Times Cited: 5
Undiagnosed RASopathies in infertile men
Anna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 3
Anna-Grete Juchnewitsch, Kristjan Pomm, Avirup Dutta, et al.
Frontiers in Endocrinology (2024) Vol. 15
Open Access | Times Cited: 3
Abnormalities of pubertal development and gonadal function in Noonan syndrome
Giuseppa Patti, Marco Scaglione, Nadia Gabriella Maiorano, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 7
Giuseppa Patti, Marco Scaglione, Nadia Gabriella Maiorano, et al.
Frontiers in Endocrinology (2023) Vol. 14
Open Access | Times Cited: 7
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis
Kirsten M. Farncombe, Emily Thain, Carolina Barnett‐Tapia, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 12
Kirsten M. Farncombe, Emily Thain, Carolina Barnett‐Tapia, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 12
Phenotype–genotype analysis of 242 individuals with RASopathies : 18‐year experience of a tertiary center in Brazil
Débora Romeo Bertola, Matheus Augusto Araújo Castro, Guilherme Lopes Yamamoto, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2020) Vol. 184, Iss. 4, pp. 896-911
Closed Access | Times Cited: 18
Débora Romeo Bertola, Matheus Augusto Araújo Castro, Guilherme Lopes Yamamoto, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2020) Vol. 184, Iss. 4, pp. 896-911
Closed Access | Times Cited: 18
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Archana Rai, Jonathan Klonowski, Bo Yuan, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
New insights into the molecular basis of spinal neurofibromatosis type 1
Paola Bettinaglio, Eleonora Mangano, Viviana Tritto, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 8, pp. 931-938
Open Access | Times Cited: 2
Paola Bettinaglio, Eleonora Mangano, Viviana Tritto, et al.
European Journal of Human Genetics (2023) Vol. 31, Iss. 8, pp. 931-938
Open Access | Times Cited: 2
Genetic/epigenetic effects in NF1 microdeletion syndrome: beyond the haploinsufficiency, looking at the contribution of not deleted genes
Viviana Tritto, Paola Bettinaglio, Eleonora Mangano, et al.
Human Genetics (2024) Vol. 143, Iss. 6, pp. 775-795
Open Access
Viviana Tritto, Paola Bettinaglio, Eleonora Mangano, et al.
Human Genetics (2024) Vol. 143, Iss. 6, pp. 775-795
Open Access
Heterozygosity for loss-of-function variants in LZTR1 is associated with isolated multiple café-au-lait macules
Gioia Mastromoro, Claudia Santoro, Marialetizia Motta, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 11, pp. 101241-101241
Closed Access
Gioia Mastromoro, Claudia Santoro, Marialetizia Motta, et al.
Genetics in Medicine (2024) Vol. 26, Iss. 11, pp. 101241-101241
Closed Access
Changes of RAS Pathway Phosphorylation in Lymphoblastoid Cell Lines from Noonan Syndrome Patients Carrying Hypomorphic Variants in Two NS Genes
Viviana Tritto, Daniele Capitanio, Cecilia Gelfi, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 4035-4035
Open Access | Times Cited: 1
Viviana Tritto, Daniele Capitanio, Cecilia Gelfi, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 4035-4035
Open Access | Times Cited: 1
Structural Model for Recruitment of RIT1 to the LZTR1 E3 Ligase: Evidences from an Integrated Computational Approach
Antonella Paladino, Fulvio D’Angelo, Teresa Noviello, et al.
Journal of Chemical Information and Modeling (2021) Vol. 61, Iss. 4, pp. 1875-1888
Open Access | Times Cited: 3
Antonella Paladino, Fulvio D’Angelo, Teresa Noviello, et al.
Journal of Chemical Information and Modeling (2021) Vol. 61, Iss. 4, pp. 1875-1888
Open Access | Times Cited: 3
Andersen-Tawil syndrome: Overlapping clinical features with Noonan syndrome?
A.S. van der Werf - ’t Lam, Arie van Haeringen, T. Rinnen, et al.
European Journal of Medical Genetics (2021) Vol. 65, Iss. 1, pp. 104382-104382
Open Access
A.S. van der Werf - ’t Lam, Arie van Haeringen, T. Rinnen, et al.
European Journal of Medical Genetics (2021) Vol. 65, Iss. 1, pp. 104382-104382
Open Access
