Ghayda Mirzaa

8.8k total citations
56 papers, 1.7k citations indexed

About

Ghayda Mirzaa is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Ghayda Mirzaa has authored 56 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 37 papers in Molecular Biology, 32 papers in Genetics and 11 papers in Surgery. Recurrent topics in Ghayda Mirzaa's work include Genetics and Neurodevelopmental Disorders (13 papers), Genomics and Rare Diseases (12 papers) and Vascular Malformations and Hemangiomas (10 papers). Ghayda Mirzaa is often cited by papers focused on Genetics and Neurodevelopmental Disorders (13 papers), Genomics and Rare Diseases (12 papers) and Vascular Malformations and Hemangiomas (10 papers). Ghayda Mirzaa collaborates with scholars based in United States, Germany and Canada. Ghayda Mirzaa's co-authors include William B. Dobyns, Annapurna Poduri, Alex R. Paciorkowski, Susan L. Christian, John M. Graham, Karen W. Gripp, Robert L. Conway, Filomena Pirozzi, Carissa Adams and Sarah Collins and has published in prestigious journals such as Journal of Biological Chemistry, Genes & Development and PLoS ONE.

In The Last Decade

Ghayda Mirzaa

54 papers receiving 1.6k citations

Peers

Ghayda Mirzaa

GENET

PPCH

SURGE

Grazia M.S. Mancini Netherlands

Takeshi Mizuguchi Japan

Jennifer L. Silhavy United States

Kaya Bilgüvar United States

Ginevra Zanni Italy

Shalini N. Jhangiani United States

Renaud Touraine France

David Geneviève France

Armand Bottani Switzerland

Keiko Shimojima Japan

Grazia M.S. Mancini Netherlands

Ghayda Mirzaa

849 ×1.0

681 ×1.0

GENET

297 ×1.0

PPCH

203 ×0.8

SURGE

285 ×1.2

Citations per year, relative to Ghayda Mirzaa Ghayda Mirzaa (= 1×) peers Grazia M.S. Mancini

Countries citing papers authored by Ghayda Mirzaa

Since Specialization

Citations

This map shows the geographic impact of Ghayda Mirzaa's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ghayda Mirzaa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ghayda Mirzaa more than expected).

Fields of papers citing papers by Ghayda Mirzaa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ghayda Mirzaa. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ghayda Mirzaa. The network helps show where Ghayda Mirzaa may publish in the future.

Co-authorship network of co-authors of Ghayda Mirzaa

This figure shows the co-authorship network connecting the top 25 collaborators of Ghayda Mirzaa. A scholar is included among the top collaborators of Ghayda Mirzaa based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ghayda Mirzaa. Ghayda Mirzaa is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Adam, Nina, et al.. (2025). Evaluation of Targeted Therapies Currently Available for Congenital Genetic Conditions Indexed in GeneReviews . American Journal of Medical Genetics Part C Seminars in Medical Genetics. 199(3). 143–150. 2 indexed citations

Šulc, Josef, et al.. (2023). Protein interaction network analysis of mTOR signaling reveals modular organization. Journal of Biological Chemistry. 299(11). 105271–105271.

Stence, Nicholas, Kristen Park, Margarita Sáenz, et al.. (2023). Variants in PTEN Are Associated With a Diverse Spectrum of Cortical Dysplasia. Pediatric Neurology. 147. 154–162. 2 indexed citations

Timms, Andrew E., Xiao Fan, Kimberly Foss, et al.. (2022). Clinical, neuroimaging and molecular characteristics of PPP2R5D-related neurodevelopmental disorders: an expanded series with functional characterisation and genotype–phenotype analysis. Journal of Medical Genetics. 60(5). 511–522. 15 indexed citations

Mirzaa, Ghayda, et al.. (2022). Brain Abnormalities in PIK3CA-Related Overgrowth Spectrum: Physician, Patient, and Caregiver Experiences. Advances in Therapy. 39(9). 3871–3880. 3 indexed citations

Pirozzi, Filomena, Nicole Horsley, William B. Dobyns, et al.. (2021). Proximal variants in CCND2 associated with microcephaly, short stature, and developmental delay: A case series and review of inverse brain growth phenotypes. American Journal of Medical Genetics Part A. 185(9). 2719–2738. 16 indexed citations

Douzgou, Sofia, Eulàlia Baselga, Moise Danielpour, et al.. (2021). A standard of care for individuals with PIK3CA ‐related disorders: An international expert consensus statement. Clinical Genetics. 101(1). 32–47. 20 indexed citations

Garzón, Maria C., Ilona J. Frieden, Catherine E. Cottrell, et al.. (2021). Cutaneous vascular anomalies associated with a mosaic variant of AKT3: Genetic analysis continues to refine the diagnosis, nomenclature, and classification of vascular anomalies. Journal of the American Academy of Dermatology. 87(1). 162–164. 7 indexed citations

Jensen, Dana M., Victoria Dmyterko, Randall A. Bly, et al.. (2020). Cell-free DNA as a diagnostic analyte for molecular diagnosis of vascular malformations. Genetics in Medicine. 23(1). 123–130. 32 indexed citations

10.

Shi, Xiuyu, Youngshin Lim, Ginam Cho, et al.. (2020). PIK3R2/Pik3r2 Activating Mutations Result in Brain Overgrowth and EEG Changes. Annals of Neurology. 88(6). 1077–1094. 10 indexed citations

11.

Link, Nichole, Hyung-Lok Chung, Angad Jolly, et al.. (2019). Mutations in ANKLE2, a ZIKA Virus Target, Disrupt an Asymmetric Cell Division Pathway in Drosophila Neuroblasts to Cause Microcephaly. Developmental Cell. 51(6). 713–729.e6. 66 indexed citations

12.

Saneto, Russell P., et al.. (2018). A neurodegenerative mitochondrial disease phenotype due to biallelic loss‐of‐function variants in PNPLA8 encoding calcium‐independent phospholipase A2γ. American Journal of Medical Genetics Part A. 176(5). 1232–1237. 18 indexed citations

13.

Chen, She, Zhizhong Li, Choong H. Lee, et al.. (2018). PARD3 dysfunction in conjunction with dynamic HIPPO signaling drives cortical enlargement with massive heterotopia. Genes & Development. 32(11-12). 763–780. 48 indexed citations

14.

Stutterd, Chloe, George McGillivray, Zornitza Stark, et al.. (2018). Polymicrogyria in association with hypoglycemia points to mutation in the mTOR pathway. European Journal of Medical Genetics. 61(12). 738–740. 11 indexed citations

15.

Gripp, Karen W., Laura Baker, Vinay Kandula, et al.. (2016). Nephroblastomatosis or Wilms tumor in a fourth patient with a somatic PIK3CA mutation. American Journal of Medical Genetics Part A. 170(10). 2559–2569. 48 indexed citations

16.

Papandreou, Apostolos, Mandy Ma, Brenda J. Barry, et al.. (2015). Familial recurrences of FOXG1‐related disorder: Evidence for mosaicism. American Journal of Medical Genetics Part A. 167(12). 3096–3102. 11 indexed citations

17.

Jansen, Laura A., Ghayda Mirzaa, Gisele E. Ishak, et al.. (2015). PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasia. Brain. 138(6). 1613–1628. 237 indexed citations

18.

Mirzaa, Ghayda, Alex R. Paciorkowski, Eric D. Marsh, et al.. (2013). CDKL5 and ARX Mutations in Males With Early-Onset Epilepsy. Pediatric Neurology. 48(5). 367–377. 37 indexed citations

19.

Mirzaa, Ghayda, Robert L. Conway, Karen W. Gripp, et al.. (2012). Megalencephaly‐capillary malformation (MCAP) and megalencephaly‐polydactyly‐polymicrogyria‐hydrocephalus (MPPH) syndromes: Two closely related disorders of brain overgrowth and abnormal brain and body morphogenesis. American Journal of Medical Genetics Part A. 158A(2). 269–291. 121 indexed citations

20.

Mirzaa, Ghayda, Nancy N. Dodge, Ian A. Glass, et al.. (2004). Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus: A Rare Brain Malformation Syndrome Associated with Mental Retardation and Seizures. Neuropediatrics. 35(6). 353–359. 45 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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