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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:

Genotype and phenotype in patients with Noonan syndrome and a RIT1 mutation
Karim Kouz, Christina Lißewski, Stephanie Spranger, et al.
Genetics in Medicine (2016) Vol. 18, Iss. 12, pp. 1226-1234
Open Access | Times Cited: 94

Showing 1-25 of 94 citing articles:

Identifying facial phenotypes of genetic disorders using deep learning
Yaron Gurovich, Yair Hanani, Omri Bar, et al.
Nature Medicine (2018) Vol. 25, Iss. 1, pp. 60-64
Closed Access | Times Cited: 608
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
EP Europace (2022) Vol. 24, Iss. 8, pp. 1307-1367
Open Access | Times Cited: 258
The RASopathy Family: Consequences of Germline Activation of the RAS/MAPK Pathway
Mylène Tajan, Romain Paccoud, Sophie Branka, et al.
Endocrine Reviews (2018) Vol. 39, Iss. 5, pp. 676-700
Open Access | Times Cited: 196
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
Heart Rhythm (2022) Vol. 19, Iss. 7, pp. e1-e60
Open Access | Times Cited: 158
Noonan syndrome: improving recognition and diagnosis
Martin Zenker, Thomas Édouard, Joanne Blair, et al.
Archives of Disease in Childhood (2022) Vol. 107, Iss. 12, pp. 1073-1078
Open Access | Times Cited: 75
Severe Lymphatic Disorder Resolved With MEK Inhibition in a Patient With Noonan Syndrome and SOS1 Mutation
Yoav Dori, Christopher L. Smith, Erin Pinto, et al.
PEDIATRICS (2020) Vol. 146, Iss. 6
Open Access | Times Cited: 82
European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases
Arthur A.M. Wilde, Christopher Semsarian, Manlio F. Márquez, et al.
Journal of Arrhythmia (2022) Vol. 38, Iss. 4, pp. 491-553
Open Access | Times Cited: 41
Elucidation of MRAS-mediated Noonan syndrome with cardiac hypertrophy
Erin M. Higgins, J. Martijn Bos, Heather Mason‐Suares, et al.
JCI Insight (2017) Vol. 2, Iss. 5
Open Access | Times Cited: 83
Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome
Yline Capri, Elisabetta Flex, Oliver H.F. Krumbach, et al.
The American Journal of Human Genetics (2019) Vol. 104, Iss. 6, pp. 1223-1232
Open Access | Times Cited: 64
Genetic Basis of Human Congenital Heart Disease
Shannon N. Nees, Wendy K. Chung
Cold Spring Harbor Perspectives in Biology (2019) Vol. 12, Iss. 9, pp. a036749-a036749
Open Access | Times Cited: 60
Prenatal ultrasound findings of rasopathies in a cohort of 424 fetuses: update on genetic testing in the NGS era
Kyra E. Stuurman, Marieke Joosten, Ineke van der Burgt, et al.
Journal of Medical Genetics (2019) Vol. 56, Iss. 10, pp. 654-661
Open Access | Times Cited: 55
Genotype‐cardiac phenotype correlations in a large single‐center cohort of patients affected by RASopathies: Clinical implications and literature review
Chiara Leoni, Rita Blandino, Angelica Bibiana Delogu, et al.
American Journal of Medical Genetics Part A (2021) Vol. 188, Iss. 2, pp. 431-445
Closed Access | Times Cited: 44
Cardiovascular disease in Noonan syndrome
Mary Ella Pierpont, M. Cristina Digilio
Current Opinion in Pediatrics (2018) Vol. 30, Iss. 5, pp. 601-608
Closed Access | Times Cited: 59
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathy
Marialetizia Motta, Lena Sagi‐Dain, Oliver H.F. Krumbach, et al.
Human Molecular Genetics (2019) Vol. 29, Iss. 11, pp. 1772-1783
Closed Access | Times Cited: 43
Molecular and phenotypic spectrum of Noonan syndrome in Chinese patients
Xin Li, Ruen Yao, Xin Tan, et al.
Clinical Genetics (2019) Vol. 96, Iss. 4, pp. 290-299
Closed Access | Times Cited: 43
Lymphatic Abnormalities in Noonan Syndrome Spectrum Disorders: A Systematic Review
Julia Sleutjes, Lotte E. R. Kleimeier, Erika Leenders, et al.
Molecular Syndromology (2021) Vol. 13, Iss. 1, pp. 1-11
Open Access | Times Cited: 34
Succesful MEK-inhibition of severe hypertrophic cardiomyopathy in RIT1-related Noonan Syndrome
Anne Leegaard, Pernille A. Gregersen, Trine Østergaard Nielsen, et al.
European Journal of Medical Genetics (2022) Vol. 65, Iss. 11, pp. 104630-104630
Open Access | Times Cited: 28
MR lymphangiography of lymphatic abnormalities in children and adults with Noonan syndrome
Claus C. Pieper, Julia Wagenpfeil, Andreas Henkel, et al.
Scientific Reports (2022) Vol. 12, Iss. 1
Open Access | Times Cited: 24
Cognitive Phenotype and Psychopathology in Noonan Syndrome Spectrum Disorders through Various Ras/MAPK Pathway Associated Gene Variants
Ellen Wingbermühle, Renée L. Roelofs, Wouter Oomens, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 16, pp. 4735-4735
Open Access | Times Cited: 19
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
What Is New in Genetics of Congenital Heart Defects?
M. Cristina Digilio, Bruno Marino
Frontiers in Pediatrics (2016) Vol. 4
Open Access | Times Cited: 37
RIT1 controls actin dynamics via complex formation with RAC1/CDC42 and PAK1
Uta Meyer zum Büschenfelde, Laura Brandenstein, Leonie von Elsner, et al.
PLoS Genetics (2018) Vol. 14, Iss. 5, pp. e1007370-e1007370
Open Access | Times Cited: 34
Investigating the possible connection between cystic hygroma, nuchal translucency, and the genetic link underlying cardiac lymphatic abnormalities and congenital heart disease: is there an association?
Marios Loukas, Ishank Gupta, Brenna Wilson, et al.
Cardiology in the Young (2025), pp. 1-7
Closed Access
Update on the Clinical and Molecular Characterization of Noonan Syndrome and Other RASopathies: A Retrospective Study and Systematic Review
G.J. Reynolds, Andrea Gazzin, Diana Carli, et al.
International Journal of Molecular Sciences (2025) Vol. 26, Iss. 8, pp. 3515-3515
Open Access
DeepGestalt - Identifying Rare Genetic Syndromes Using Deep Learning
Yaron Gurovich, Yair Hanani, Omri Bar, et al.
arXiv (Cornell University) (2018)
Open Access | Times Cited: 28
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