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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:

Holoprosencephaly: Review of Embryology, Clinical Phenotypes, Etiology and Management
Maísa Malta, Rowim AlMutiri, Christine Saint Martin, et al.
Children (2023) Vol. 10, Iss. 4, pp. 647-647
Open Access | Times Cited: 19

Showing 19 citing articles:

Lobar holoprosencephaly with associated meningocele: A rare case report of a 25-year-old patient with multiple seizures
Parishmita Barman, Gaurav Mishra, Ganesh Murugan, et al.
Radiology Case Reports (2025) Vol. 20, Iss. 4, pp. 2004-2008
Closed Access
Congenital external hydrocephalus: A rare presentation of lobar holoprosencephaly in a neonate
Rakshanda Agrawal, Nishant Raj, Vaishali Dhawan, et al.
Radiology Case Reports (2025) Vol. 20, Iss. 5, pp. 2323-2327
Closed Access
Developmental, Endocrine and Ophthalmologic Outcomes in Children Prenatally Diagnosed with Midline Brain Malformations
McKenna L Coletti, Jennifer C. Keene, Allison Smego, et al.
Pediatric Neurology (2025)
Closed Access
The Fuzzy planar cell polarity protein (FUZ), necessary for primary cilium formation, is essential for pituitary development
Emily J. Lodge, William B. Barrell, Karen Liu, et al.
Journal of Anatomy (2023) Vol. 244, Iss. 2, pp. 358-367
Open Access | Times Cited: 7
Use of an Orthodontic and Otolaryngological Approach in an Infant with Holoprosencephaly
Angela Galeotti, Giovanni Carlo De Vincentiis, Emanuela Sitzia, et al.
Children (2024) Vol. 11, Iss. 5, pp. 554-554
Open Access | Times Cited: 2
Prdm15 acts upstream of Wnt4 signaling in anterior neural development of Xenopus laevis
Ernestine Saumweber, Slim Mzoughi, Arin Khadra, et al.
Frontiers in Cell and Developmental Biology (2024) Vol. 12
Open Access | Times Cited: 2
Holoprosencephaly
Thierry A.G.M. Huisman, Thierry A.G.M. Huisman
Newborn (2024) Vol. 3, Iss. 1, pp. 45-60
Open Access | Times Cited: 1
Malformaciones del sistema nervioso central asociadas a embriopatía diabética en madres latinoamericanas sin control glicémico: Una revisión
Gilson Zelada-Bran, Ana Celada-Barrios, Jarmila Liska de León, et al.
Revista Internacional de Salud Materno Fetal (2024), pp. r1-r17
Open Access | Times Cited: 1
Utilidad del complejo posterior para el diagnóstico prenatal de sintelencefalia
Fernando Nuez Viñals, Cecilia Okuma, Lucía García Vega, et al.
Revista chilena de obstetricia y ginecología (2024) Vol. 89, Iss. 1
Open Access
To Save Babies, We Need a Team – Let\'s Build One!
Akhil Maheshwari, Mario Motta, Kei Lui
Newborn (2024) Vol. 3, Iss. 1, pp. iv-vii
Open Access
Prenatal identification of a pathogenic maternal FGFR1 variant in two consecutive pregnancies with fetal forebrain malformations
Ludovico Graziani, Sara Nuovo, Elisa Pisaneschi, et al.
The Journal of Maternal-Fetal & Neonatal Medicine (2024) Vol. 37, Iss. 1
Open Access
CNOT1 p.Arg535Cys variant in holoprosencephaly with late onset diabetes mellitus
Amaro Freire de Queiroz Júnior, Maria Teresa Vieira Sanseverino, Marcus Vinícius Martins Collares, et al.
American Journal of Medical Genetics Part A (2024) Vol. 194, Iss. 12
Closed Access
Lobar holoprosencephaly
Arlene Campos, Pedro Ramírez
Radiopaedia.org (2024)
Closed Access
The Role of Antenatal Ultrasound Scans in the Early Detection of Alobar Holoprosencephaly: A Case Report
Mariam E Mohamed, Shymaa R Ahmed, Elsayed M Elsayed Ahmed, et al.
Cureus (2024)
Open Access
Holoprosencephaly: Review of the literature and Practical Recommendations for Pediatric Neurologists
Barbara Scelsa, Dawn Gano, Anthony R Hart, et al.
Pediatric Neurology (2024) Vol. 162, pp. 87-96
Closed Access
A Review of Neurogenetics in Fetal and Neonatal Clinical Medicine
Amitha Ananth, Michael A. Lopez
Seminars in Fetal and Neonatal Medicine (2024), pp. 101550-101550
Closed Access
Alobar Holoprosencephaly and Cebocephaly in a Newborn
Mark P. Roy, Jyotsna Shrivastava, Pratibha Bamne, et al.
Indian Pediatrics Case Reports (2024) Vol. 4, Iss. 4, pp. 260-261
Open Access
Alobar Holoprosencephaly in a Newborn: A Case Report of Prenatal Diagnosis and a Review of the Literature
Kamal Chafiq, Khalil Toumi, Fatima Ezzahra Khayi, et al.
Cureus (2024)
Open Access
Rare Maternal Structural Mosaicism as a Familial Cause of 18p Deletion Syndrome: Cytogenetics Mechanisms and Phenotypic Variability
Ana Emirene Montes, Ingrid Tavares de Lima, Thais Freitas Barreto Fernandes, et al.
International Journal of Genetics and Genomics (2024) Vol. 12, Iss. 4, pp. 81-85
Open Access
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