
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:
Genetics etiologies and genotype phenotype correlations in a cohort of individuals with central conducting lymphatic anomaly
Mandi Liu, Christopher L. Smith, David M. Biko, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 9, pp. 1022-1028
Open Access | Times Cited: 21
Mandi Liu, Christopher L. Smith, David M. Biko, et al.
European Journal of Human Genetics (2022) Vol. 30, Iss. 9, pp. 1022-1028
Open Access | Times Cited: 21
Showing 21 citing articles:
Genomic profiling informs diagnoses and treatment in vascular anomalies
Dong Li, Sarah E. Sheppard, Michael March, et al.
Nature Medicine (2023) Vol. 29, Iss. 6, pp. 1530-1539
Open Access | Times Cited: 32
Dong Li, Sarah E. Sheppard, Michael March, et al.
Nature Medicine (2023) Vol. 29, Iss. 6, pp. 1530-1539
Open Access | Times Cited: 32
Lymphatic malformations: mechanistic insights and evolving therapeutic frontiers
Milena Petkova, Ingvar Ferby, Taija Mäkinen
Journal of Clinical Investigation (2024) Vol. 134, Iss. 6
Open Access | Times Cited: 9
Milena Petkova, Ingvar Ferby, Taija Mäkinen
Journal of Clinical Investigation (2024) Vol. 134, Iss. 6
Open Access | Times Cited: 9
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibition
Sarah E. Sheppard, Michael March, Christoph Seiler, et al.
JCI Insight (2023) Vol. 8, Iss. 9
Open Access | Times Cited: 19
Sarah E. Sheppard, Michael March, Christoph Seiler, et al.
JCI Insight (2023) Vol. 8, Iss. 9
Open Access | Times Cited: 19
Investigation into the genetics of fetal congenital lymphatic anomalies
Daniella Rogerson, Anna Alkelai, Jessica L. Giordano, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 6, pp. 703-716
Open Access | Times Cited: 17
Daniella Rogerson, Anna Alkelai, Jessica L. Giordano, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 6, pp. 703-716
Open Access | Times Cited: 17
Central conducting lymphatic anomaly: from bench to bedside
Luciana Daniela Garlisi Torales, Benjamin A Sempowski, Georgia L. Krikorian, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 8
Open Access | Times Cited: 8
Luciana Daniela Garlisi Torales, Benjamin A Sempowski, Georgia L. Krikorian, et al.
Journal of Clinical Investigation (2024) Vol. 134, Iss. 8
Open Access | Times Cited: 8
Dysregulation of Lymphatic Endothelial VEGFR3 Signaling in Disease
Kevin Kuonqui, Adana-Christine Campbell, Ananta Sarker, et al.
Cells (2023) Vol. 13, Iss. 1, pp. 68-68
Open Access | Times Cited: 16
Kevin Kuonqui, Adana-Christine Campbell, Ananta Sarker, et al.
Cells (2023) Vol. 13, Iss. 1, pp. 68-68
Open Access | Times Cited: 16
Pathogenic variants inPIK3CAare associated with clinical phenotypes of kaposiform lymphangiomatosis, generalized lymphatic anomaly, and central conducting lymphatic anomaly
Jeremy Grenier, Alexandra J. Borst, Sarah E. Sheppard, et al.
Pediatric Blood & Cancer (2023) Vol. 70, Iss. 9
Open Access | Times Cited: 12
Jeremy Grenier, Alexandra J. Borst, Sarah E. Sheppard, et al.
Pediatric Blood & Cancer (2023) Vol. 70, Iss. 9
Open Access | Times Cited: 12
Lymphatische Malformationen im Kindes- und Jugendalter
A Groteklaes, Andreas Müller
Deleted Journal (2025)
Closed Access
A Groteklaes, Andreas Müller
Deleted Journal (2025)
Closed Access
Lymphatic malformation:Classification, Pathogenesis and Therapeutic Strategies
Chaonan Zhang, Jing Liu, Yao Wang, et al.
Annals of Vascular Surgery (2025)
Closed Access
Chaonan Zhang, Jing Liu, Yao Wang, et al.
Annals of Vascular Surgery (2025)
Closed Access
Hyperactive KRAS/MAPK signaling disrupts normal lymphatic vessel architecture and function
Lorenzo M. Fernandes, Jeffrey D. Tresemer, Jing Zhang, et al.
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 7
Lorenzo M. Fernandes, Jeffrey D. Tresemer, Jing Zhang, et al.
Frontiers in Cell and Developmental Biology (2023) Vol. 11
Open Access | Times Cited: 7
Complex lymphatic anomalies: Molecular landscape and medical management
Alexandra J. Borst, Allison Britt, Denise M. Adams
Seminars in Pediatric Surgery (2024) Vol. 33, Iss. 3, pp. 151422-151422
Closed Access | Times Cited: 2
Alexandra J. Borst, Allison Britt, Denise M. Adams
Seminars in Pediatric Surgery (2024) Vol. 33, Iss. 3, pp. 151422-151422
Closed Access | Times Cited: 2
Trametinib restores the central conducting lymphatic flow in a premature infant with Noonan syndrome
Erika Leenders, Lotte E. R. Kleimeier, Lauren C. Weeke, et al.
Clinical Case Reports (2024) Vol. 12, Iss. 7
Open Access | Times Cited: 2
Erika Leenders, Lotte E. R. Kleimeier, Lauren C. Weeke, et al.
Clinical Case Reports (2024) Vol. 12, Iss. 7
Open Access | Times Cited: 2
Mosaic RASopathies: A review of disorders caused by somatic pathogenic variants in the genes of the RAS/MAPK pathway
Diana Carli, Nicoletta Resta, Giovanni Battista Ferrero, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 520-529
Closed Access | Times Cited: 8
Diana Carli, Nicoletta Resta, Giovanni Battista Ferrero, et al.
American Journal of Medical Genetics Part C Seminars in Medical Genetics (2022) Vol. 190, Iss. 4, pp. 520-529
Closed Access | Times Cited: 8
Neonatal perspective on central lymphatic disorders
Brian M. Dulmovits, Dalal Taha
Seminars in Pediatric Surgery (2024) Vol. 33, Iss. 3, pp. 151424-151424
Closed Access | Times Cited: 1
Brian M. Dulmovits, Dalal Taha
Seminars in Pediatric Surgery (2024) Vol. 33, Iss. 3, pp. 151424-151424
Closed Access | Times Cited: 1
Surgical creation of lymphocutaneous fistulas for the management of infants with central lymphatic obstruction
Pablo Laje, Benjamin Smood, Christopher L. Smith, et al.
Pediatric Surgery International (2023) Vol. 39, Iss. 1
Closed Access | Times Cited: 3
Pablo Laje, Benjamin Smood, Christopher L. Smith, et al.
Pediatric Surgery International (2023) Vol. 39, Iss. 1
Closed Access | Times Cited: 3
Lymphatic failure and lymphatic interventions: knowledge gaps and future directions for a new frontier in congenital heart disease
Benjamin Smood, Christopher L. Smith, Yoav Dori, et al.
Seminars in Pediatric Surgery (2024) Vol. 33, Iss. 3, pp. 151426-151426
Closed Access
Benjamin Smood, Christopher L. Smith, Yoav Dori, et al.
Seminars in Pediatric Surgery (2024) Vol. 33, Iss. 3, pp. 151426-151426
Closed Access
The utility of dynamic contrast-enhanced intranodal magnetic resonance lymphangiography (MRL) in the investigation of primary lymphatic anomalies
Lakshmi Ratnam, Michael Mills, Anita Wale, et al.
Clinical Radiology (2024) Vol. 79, Iss. 10, pp. e1180-e1188
Open Access
Lakshmi Ratnam, Michael Mills, Anita Wale, et al.
Clinical Radiology (2024) Vol. 79, Iss. 10, pp. e1180-e1188
Open Access
Central Conducting Lymphatic Anomalies
Hui‐Qi Qu, Dong Li, Hákon Hákonarson
(2024), pp. 215-239
Closed Access
Hui‐Qi Qu, Dong Li, Hákon Hákonarson
(2024), pp. 215-239
Closed Access
Molecular landscape and classification of vascular anomalies
Emmanuel Seront, Angela Queisser, Laurence M. Boon, et al.
Hematology (2024) Vol. 2024, Iss. 1, pp. 700-708
Closed Access
Emmanuel Seront, Angela Queisser, Laurence M. Boon, et al.
Hematology (2024) Vol. 2024, Iss. 1, pp. 700-708
Closed Access
Persistent chylothorax associated with lymphatic malformation type 6 due to biallelic pathogenic variants in PIEZO1
Thomas Kovesi, Samantha K. Rojas, Kym M. Boycott
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 8, pp. 2188-2192
Closed Access
Thomas Kovesi, Samantha K. Rojas, Kym M. Boycott
American Journal of Medical Genetics Part A (2023) Vol. 191, Iss. 8, pp. 2188-2192
Closed Access
Guidelines, guidelines everywhere—and still I’m not sure what to do
Alisdair McNeill
European Journal of Human Genetics (2022) Vol. 30, Iss. 9, pp. 989-990
Open Access
Alisdair McNeill
European Journal of Human Genetics (2022) Vol. 30, Iss. 9, pp. 989-990
Open Access