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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:

When to test fetuses for RASopathies? Proposition from a systematic analysis of 352 multicenter cases and a postnatal cohort
Alexandra MS Scott, Niccolò Di Giosaffatte, Valentina Pinna, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 6, pp. 1116-1124
Open Access | Times Cited: 31

Showing 1-25 of 31 citing articles:

The RASopathies: from pathogenetics to therapeutics
Katie E. Hebron, Edjay R. Hernandez, Marielle E. Yohe
Disease Models & Mechanisms (2022) Vol. 15, Iss. 2
Open Access | Times Cited: 117
Clinical overview on RASopathies
Martin Zenker
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 414-424
Open Access | Times Cited: 51
Trametinib as a targeted treatment in cardiac and lymphatic presentations of Noonan syndrome
Isabel De Brouchoven, Juan Lorand, Léon Bofferding, et al.
Frontiers in Pediatrics (2025) Vol. 13
Open Access | Times Cited: 1
Defining the variant-phenotype correlation in patients affected by Noonan syndrome with the RAF1:c.770C>T p.(Ser257Leu) variant
Andrea Gazzin, Federico Fornari, Marcello Niceta, et al.
European Journal of Human Genetics (2024) Vol. 32, Iss. 8, pp. 964-971
Closed Access | Times Cited: 5
The heart in RASopathies
Angelica Bibiana Delogu, Giuseppe Limongelli, Paolo Versacci, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 440-451
Closed Access | Times Cited: 19
Prenatal diagnosis by trio exome sequencing in fetuses with ultrasound anomalies: A powerful diagnostic tool
Frédéric Tran Mau‐Them, Julian Delanne, Anne‐Sophie Denommé‐Pichon, et al.
Frontiers in Genetics (2023) Vol. 14
Open Access | Times Cited: 12
RASopathies and cardiac manifestations
Nazia Hilal, Zi Chen, Ming Hui Chen, et al.
Frontiers in Cardiovascular Medicine (2023) Vol. 10
Open Access | Times Cited: 12
Fetal Hydrops: Genetic Dissection of an Unspecific Sonographic Finding—A Comprehensive Review
Gioia Mastromoro, Daniele Guadagnolo, Alessandro De Luca, et al.
Diagnostics (2025) Vol. 15, Iss. 4, pp. 465-465
Open Access
Whole Genome Sequencing in Prenatal Diagnostics: The Danish Approach to Guideline Formation and Implementation Within Public Healthcare
Ida Vogel, Lotte Andreasen, Marie Balslev‐Harder, et al.
Prenatal Diagnosis (2025)
Open Access
Cardiovascular aspects of Noonan syndrome and related disorders
Martin Zenker, Cordula M. Wolf
Medizinische Genetik (2025) Vol. 37, Iss. 2, pp. 113-124
Closed Access
RASopathies: Evolving Concepts in Pathogenetics, Clinical Features, and Management
Jigna Padhiyar, Rahul Mahajan, Maitreyee Panda
Indian Dermatology Online Journal (2024) Vol. 15, Iss. 3, pp. 392-404
Open Access | Times Cited: 2
Increased nuchal translucency after low‐risk noninvasive prenatal testing: What should we tell prospective parents?
Joanne Kelley, George McGillivray, Simon Meagher, et al.
Prenatal Diagnosis (2021) Vol. 41, Iss. 10, pp. 1305-1315
Open Access | Times Cited: 15
Lymphatic anomalies during lifetime in patients with Noonan syndrome: Retrospective cohort study
Jessie W. Swarts, Lotte E. R. Kleimeier, Erika Leenders, et al.
American Journal of Medical Genetics Part A (2022) Vol. 188, Iss. 11, pp. 3242-3261
Open Access | Times Cited: 11
A Pain in the Neck: Lessons Learnt from Genetic Testing in Fetuses Detected with Nuchal Fluid Collections, Increased Nuchal Translucency versus Cystic Hygroma—Systematic Review of the Literature, Meta-Analysis and Case Series
Gioia Mastromoro, Daniele Guadagnolo, Nader Khaleghi Hashemian, et al.
Diagnostics (2022) Vol. 13, Iss. 1, pp. 48-48
Open Access | Times Cited: 11
Prenatal Diagnosis by Trio Clinical Exome Sequencing: Single Center Experience
Katia Margiotti, Marco Fabiani, Antonella Cima, et al.
Current Issues in Molecular Biology (2024) Vol. 46, Iss. 4, pp. 3209-3217
Open Access | Times Cited: 1
Outcomes of pregnancies with varying levels of nuchal translucency measurements: A population‐based retrospective study in Ontario, Canada
Kara Bellai‐Dussault, Shelley Dougan, Deshayne B. Fell, et al.
Acta Obstetricia Et Gynecologica Scandinavica (2024) Vol. 103, Iss. 12, pp. 2499-2510
Open Access | Times Cited: 1
The RRAS2 pathogenic variant p.Q72L produces severe Noonan syndrome with hydrocephalus: A case report
Nadav I. Weinstock, Laurie S. Sadler
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 1, pp. 364-368
Closed Access | Times Cited: 8
Prenatal Diagnosis of Euploid Increased Nuchal Translucency on Fetal Ultrasound (II)
Chih‐Ping Chen
Journal of Medical Ultrasound (2023) Vol. 31, Iss. 1, pp. 13-16
Open Access | Times Cited: 3
Prenatal whole‐exome sequencing in fetuses with increased nuchal translucency
C Cao, Fang Liu, Yan Yang, et al.
Molecular Genetics & Genomic Medicine (2023) Vol. 11, Iss. 11
Open Access | Times Cited: 3
Prenatal diagnosis of autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants presented with thick nuchal translucency and cardiac abnormalities
Qiuxia Yu, Zhen Li, Xiao‐Mei Lin, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 13, pp. 1662-1665
Closed Access | Times Cited: 2
RASopathies due to de novo pathogenic variants: clinical features, genetic findings and outcomes in nine neonates born with congenital heart defects
Simin Zheng, Huanyang Huang, Li Ma, et al.
BMC Medical Genomics (2022) Vol. 15, Iss. 1
Open Access | Times Cited: 4
European Medical Education Initiative on Noonan syndrome: A clinical practice survey assessing the diagnosis and clinical management of individuals with Noonan syndrome across Europe
Sixto García‐Miñaúr, Emma Burkitt‐Wright, Alain Verloès, et al.
European Journal of Medical Genetics (2021) Vol. 65, Iss. 1, pp. 104371-104371
Open Access | Times Cited: 5
Obstetrical and neonatal outcomes of cardio‐facio‐cutaneous syndrome: Prenatal consequences of Ras/MAPK dysregulation
Angie C. Jelin, Amanda Mahle, Susan H Tran, et al.
American Journal of Medical Genetics Part A (2022) Vol. 191, Iss. 2, pp. 323-331
Open Access | Times Cited: 3
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
New Insights Into the Spectrum of RASopathies: Clinical and Genetic Data in a Cohort of 121 Spanish Patients
Ana Isabel Sánchez Barbero, Irene Valenzuela, Paula Fernández‐Álvarez, et al.
American Journal of Medical Genetics Part A (2024)
Open Access
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