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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:

Noonan syndrome
Amy E. Roberts, Judith Allanson, Marco Tartaglia, et al.
The Lancet (2013) Vol. 381, Iss. 9863, pp. 333-342
Open Access | Times Cited: 691

Showing 1-25 of 691 citing articles:

2023 ESC Guidelines for the management of cardiomyopathies
Elena Arbelo, Alexandros Protonotarios, Juan R. Gimeno, et al.
European Heart Journal (2023) Vol. 44, Iss. 37, pp. 3503-3626
Open Access | Times Cited: 1038
Compromised MAPK signaling in human diseases: an update
Eun‐Kyung Kim, Eui‐Ju Choi
Archives of Toxicology (2015) Vol. 89, Iss. 6, pp. 867-882
Closed Access | Times Cited: 916
Targeting RAF kinases for cancer therapy: BRAF-mutated melanoma and beyond
Matthew Holderfield, Marian M. Deuker, Frank McCormick, et al.
Nature reviews. Cancer (2014) Vol. 14, Iss. 7, pp. 455-467
Open Access | Times Cited: 768
Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association
Mary Ella Pierpont, Martina Brueckner, Wendy K. Chung, et al.
Circulation (2018) Vol. 138, Iss. 21
Open Access | Times Cited: 525
Using high-resolution variant frequencies to empower clinical genome interpretation
Nicola Whiffin, Eric Vallabh Minikel, Roddy Walsh, et al.
Genetics in Medicine (2017) Vol. 19, Iss. 10, pp. 1151-1158
Open Access | Times Cited: 408
Pilocytic astrocytoma: pathology, molecular mechanisms and markers
V. Peter Collins, David Jones, Caterina Giannini
Acta Neuropathologica (2015) Vol. 129, Iss. 6, pp. 775-788
Open Access | Times Cited: 403
Portrait of the PI3K/AKT pathway in colorectal cancer
Stine A. Danielsen, Peter W. Eide, Arild Nesbakken, et al.
Biochimica et Biophysica Acta (BBA) - Reviews on Cancer (2014) Vol. 1855, Iss. 1, pp. 104-121
Closed Access | Times Cited: 302
Cardiomyopathy in Children: Classification and Diagnosis: A Scientific Statement From the American Heart Association
Steven E. Lipshultz, Yuk M. Law, Alfred Asante‐Korang, et al.
Circulation (2019) Vol. 140, Iss. 1
Open Access | Times Cited: 292
Short and tall stature: a new paradigm emerges
Jeffrey Baron, Lars Sävendahl, Francesco De Luca, et al.
Nature Reviews Endocrinology (2015) Vol. 11, Iss. 12, pp. 735-746
Open Access | Times Cited: 266
Role of multimodality cardiac imaging in the management of patients with hypertrophic cardiomyopathy: an expert consensus of the European Association of Cardiovascular Imaging Endorsed by the Saudi Heart Association
Nuno Cardim, Maurizio Galderisi, Thor Edvardsen, et al.
European Heart Journal - Cardiovascular Imaging (2015) Vol. 16, Iss. 3, pp. 280-280
Open Access | Times Cited: 256
Leukaemogenic effects of Ptpn11 activating mutations in the stem cell microenvironment
Lei Dong, Wen-Mei Yu, Hong Zheng, et al.
Nature (2016) Vol. 539, Iss. 7628, pp. 304-308
Open Access | Times Cited: 234
SHP2 sails from physiology to pathology
Mylène Tajan, Audrey de Rocca Serra, Philippe Valet, et al.
European Journal of Medical Genetics (2015) Vol. 58, Iss. 10, pp. 509-525
Closed Access | Times Cited: 214
<p>Some of the Factors Involved in Male Infertility: A Prospective Review</p>
Emad Babakhanzadeh, Majid Nazari, Sina Ghasemifar, et al.
International Journal of General Medicine (2020) Vol. Volume 13, pp. 29-41
Open Access | Times Cited: 211
Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA
Jinglan Zhang, Jianli Li, Jennifer Saucier, et al.
Nature Medicine (2019) Vol. 25, Iss. 3, pp. 439-447
Closed Access | Times Cited: 205
Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes
Christian P. Kratz, Lude Franke, Harm Peters, et al.
British Journal of Cancer (2015) Vol. 112, Iss. 8, pp. 1392-1397
Open Access | Times Cited: 197
HSF1: Guardian of Proteostasis in Cancer
Chengkai Dai, Stephen B. Sampson
Trends in Cell Biology (2015) Vol. 26, Iss. 1, pp. 17-28
Open Access | Times Cited: 197
Intestinal lymphatic vasculature: structure, mechanisms and functions
Jeremiah Bernier‐Latmani, Tatiana V. Petrova
Nature Reviews Gastroenterology & Hepatology (2017) Vol. 14, Iss. 9, pp. 510-526
Closed Access | Times Cited: 191
The Diagnosis and Management of Neurofibromatosis Type 1
Ina Ly, Jaishri O. Blakeley
Medical Clinics of North America (2019) Vol. 103, Iss. 6, pp. 1035-1054
Closed Access | Times Cited: 177
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
Next-generation sequencing identifies rare variants associated with Noonan syndrome
Peng‐Chieh Chen, Jiani C. Yin, Hui-Wen Yu, et al.
Proceedings of the National Academy of Sciences (2014) Vol. 111, Iss. 31, pp. 11473-11478
Open Access | Times Cited: 175
MECHANISMS IN ENDOCRINOLOGY: Novel genetic causes of short stature
Jan M. Wit, Wilma Oostdijk, Monique Losekoot, et al.
European Journal of Endocrinology (2015) Vol. 174, Iss. 4, pp. R145-R173
Open Access | Times Cited: 163
Functional Dysregulation of CDC42 Causes Diverse Developmental Phenotypes
Simone Martinelli, Oliver H.F. Krumbach, Francesca Pantaleoni, et al.
The American Journal of Human Genetics (2018) Vol. 102, Iss. 2, pp. 309-320
Open Access | Times Cited: 157
ClinGen’s RASopathy Expert Panel consensus methods for variant interpretation
Bruce D. Gelb, Hélène Cavé, Mitchell W. Dillon, et al.
Genetics in Medicine (2018) Vol. 20, Iss. 11, pp. 1334-1345
Open Access | Times Cited: 147
A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair
Karen W. Gripp, Kimberly A. Aldinger, James T. Bennett, et al.
American Journal of Medical Genetics Part A (2016) Vol. 170, Iss. 9, pp. 2237-2247
Open Access | Times Cited: 138
Cardiovascular disease in Noonan syndrome
Terence Prendiville, K. Gauvreau, Erica Tworog‐Dube, et al.
Archives of Disease in Childhood (2014) Vol. 99, Iss. 7, pp. 629-634
Open Access | Times Cited: 136
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