Mona Aglan

4.3k citations
73 papers · 1.7k · h-index 23

Impact in

  • Genetics top 2%
    • Connective tissue disorders research
    • Genetic and Kidney Cyst Diseases
  • Rheumatology top 2%
    • Bone and Dental Protein Studies

Papers in

  • Genetics 48
    • Connective tissue disorders research 26
    • Genomic variations and chromosomal abnormalities 9
  • Molecular Biology 31
    • Hedgehog Signaling Pathway Studies 6
    • RNA modifications and cancer 6
Co-authors
Samia A. Temtamy (53 shared papers)Víctor L. Ruiz‐Pérez (13 shared papers)Pablo Lapunzina (13 shared papers)José A. Caparrós‐Martín (8 shared papers)Víctor Martínez‐Glez (7 shared papers)Ghada A. Otaify (25 shared papers)Khalda Amr (10 shared papers)Adel M. Ashour (11 shared papers)
Journals
Human Mutation (5 papers)The American Journal of Human Genetics (4 papers)Osteoporosis International (3 papers)American Journal of Medical Genetics Part A (17 papers)Archives of Oral Biology (1 paper)
Partner nations
EgyptUnited StatesSpain

In The Last Decade

Mona Aglan

71 papers receiving 1.7k citations

Peers

Mona Aglan
Comparison fields: 5 of 99
  • Genetics 1.0k
  • Rheumatology 341
  • Developmental Biology 53
  • Molecular Biology 763
  • Cancer Research 142
Replace Geneviève Baujat with:
Geneviève Baujat France
Katta M. Girisha India
M. Le Merrer France
Nursel Elçioğlu Türkiye
Giedré Grigelioniené Sweden
D L Rimoin United States
Yasemin Alanay Türkiye
Ariana Kariminejad Iran
Michael B. Bober United States
Gary A. Bellus United States
Mona Aglan relative to Geneviève Baujat France Geneviève Baujat's profile →
Citations per field
00.5×1.7×
Geneviève Baujat · 1×
Citations per year

Countries citing papers authored by Mona Aglan

Since Specialization
Citations

This map shows the geographic impact of Mona Aglan'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 Mona Aglan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mona Aglan more than expected).

Fields of papers citing papers by Mona Aglan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mona Aglan. 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 Mona Aglan. The network helps show where Mona Aglan may publish in the future.

Co-authors

The 25 scholars most cited alongside Mona Aglan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mona Aglan Line = papers co-authored together Mona Aglan links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 73 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta
The American Journal of Human Genetics ·Pablo Lapunzina, Mona Aglan, Samia A. Temtamy, José A. Caparrós‐Martín, (unknown), Rocío Letón, Víctor Martínez‐Glez, Rasha M. Elhossini, Khalda Amr, Nuria Vilaboa, Víctor L. Ruiz‐Pérez
2010239
2
Identification of a mutation causing deficient BMP1/mTLD proteolytic activity in autosomal recessive osteogenesis imperfecta
Human Mutation ·Víctor Martínez‐Glez, (unknown), José A. Caparrós‐Martín, Mona Aglan, Samia A. Temtamy, Jair Tenorio, Verónica Pulido, Uschi Lindert, Marianne Rohrbach, David R. Eyre, Cecilia Giunta, Pablo Lapunzina, Víctor L. Ruiz‐Pérez
2011177
3
Mutations in EOGT Confirm the Genetic Heterogeneity of Autosomal-Recessive Adams-Oliver Syndrome
The American Journal of Human Genetics ·Ranad Shaheen, Mona Aglan, Kim M. Keppler‐Noreuil, Eissa Faqeih, Shinu Ansari, Kim Horton, Adel M. Ashour, Maha S. Zaki, Fatema Alzahrani, Anna M. Cueto‐González, Ghada M. H. Abdel‐Salam, Samia A. Temtamy, Fowzan S. Alkuraya
201396
4
Brachydactyly
Orphanet Journal of Rare Diseases ·Samia A. Temtamy, Mona Aglan
200895
5
Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum
Human Mutation ·Maria Trinidad Puig-Hervás, Samia A. Temtamy, Mona Aglan, (unknown), Víctor Martínez‐Glez, María Juliana Ballesta‐Martínez, Vanesa López‐González, Adel M. Ashour, Khalda Amr, Verónica Pulido, Encarna Guillén‐Navarro, Pablo Lapunzina, José A. Caparrós‐Martín, Víctor L. Ruiz‐Pérez
201282
6
The Primordial Growth Disorder 3-M Syndrome Connects Ubiquitination to the Cytoskeletal Adaptor OBSL1
The American Journal of Human Genetics ·Dan Hanson, Philip Murray, Amit Sud, Samia A. Temtamy, Mona Aglan, Andrea Superti‐Furga, Sue Holder, Jill Urquhart, Emma Hilton, Forbes Manson, Peter Scambler, Graeme C. Black, Peter Clayton
200981
7
A Novel Homozygous Mutation in FGFR3 Causes Tall Stature, Severe Lateral Tibial Deviation, Scoliosis, Hearing Impairment, Camptodactyly, and Arachnodactyly
Human Mutation ·Periklis Makrythanasis, Samia A. Temtamy, Mona Aglan, Ghada A. Otaify, Hanan Hamamy, Stylianos E. Antonarakis
201464
8
FAM46A mutations are responsible for autosomal recessive osteogenesis imperfecta
Journal of Medical Genetics ·Mathilde Doyard, Séverine Bacrot, Céline Huber, Maja Di Rocco, Alice Goldenberg, Mona Aglan, Perrine Brunelle, Samia A. Temtamy, Caroline Michot, Ghada A. Otaify, Coralie Haudry, Mireille Castanet, J. Leroux, Jean‐Paul Bonnefont, Arnold Münnich, Geneviève Baujat, Pablo Lapunzina, Sophie Monnot, Víctor L. Ruiz‐Pérez, Valérie Cormier‐Daire
201857
9
Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate
Disease Models & Mechanisms ·Roberta Besio, Nadia Garibaldi, Laura Leoni, Lina Cipolla, Simone Sabbioneda, Marco Biggiogera, Monica Mottes, Mona Aglan, Ghada A. Otaify, Samia A. Temtamy, Antonio Rossi, Antonella Forlino
201954
10
Widening the mutation spectrum ofEVCandEVC2: ectopic expression of Weyer variants in NIH 3T3 fibroblasts disrupts hedgehog signaling
Human Mutation ·(unknown), Pablo Lapunzina, Derek Lim, Raffaella Zannolli, Deborah Bartholdi, Bernd Wollnik, Othman Al-Ajlouni, Suhair S Eid, Helen Cox, Sabrina Buoni, (unknown), María Luisa Martínez‐Frías, (unknown), Samia A. Temtamy, Mona Aglan, Judith A. Goodship, Víctor L. Ruiz‐Pérez
200950
11
Consanguinity and genetic disorders in Egypt
Samia A. Temtamy, Mona Aglan
201250
12
Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations
American Journal of Medical Genetics Part A ·José A. Caparrós‐Martín, (unknown), Verónica Pulido, Víctor Martínez‐Glez, Inmaculada Rueda‐Arenas, Khalda Amr, Chantal Farra, Pablo Lapunzina, Víctor L. Ruiz‐Pérez, Samia A. Temtamy, Mona Aglan
201348
13
3D assessment of intervertebral disc degeneration in zebrafish identifies changes in bone density that prime disc disease
Bone Research ·Érika Kague, Francesco Turci, Elis Newman, Yushi Yang, Kate Robson Brown, Mona Aglan, Ghada A. Otaify, Samia A. Temtamy, Víctor L. Ruiz‐Pérez, Stephen Cross, C. Patrick Royall, P. Eckhard Witten, Chrissy L. Hammond
202144
14
Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium
Human Molecular Genetics ·José A. Caparrós‐Martín, Alessandro De Luca, François Cartault, Mona Aglan, Samia A. Temtamy, Ghada A. Otaify, Mennat Mehrez, (unknown), Laura Vázquez, Jean‐Luc Alessandri, Julián Nevado, Inmaculada Rueda‐Arenas, Karen E. Heath, M. Cristina Digilio, Bruno Dallapiccola, Judith A. Goodship, Pleasantine Mill, Pablo Lapunzina, Víctor L. Ruiz‐Pérez
201543
15
Long interspersed nuclear element-1 (LINE1)-mediated deletion ofEVC,EVC2,C4orf6, andSTK32B in Ellis–van Creveld syndrome with borderline intelligence
Human Mutation ·Samia A. Temtamy, Mona Aglan, (unknown), Guido Cocchi, María Pacheco, Adel M. Ashour, Khalda Amr, Sanaa M.H. Helmy, Mona El Gammal, Michael Wright, Pablo Lapunzina, Judith A. Goodship, Víctor L. Ruiz‐Pérez
200843
16
Phenotypic and cytogenetic spectrum of 9p trisomy
PubMed ·Samia A. Temtamy, Alaa K. Kamel, Samira Ismail, Nivine A. Helmy, Mona Aglan, Mona El Gammal, Mona O. El Ruby, Amal M. Mohamed
200739
17
Assessment of Pubertal Development in Egyptian Girls
Journal of Pediatric Endocrinology and Metabolism ·Laila Hosny, Mona El‐Ruby, Moushira Zaki, Mona Aglan, Maha S. Zaki, (unknown), Inas Mazen
200531
18
Zoledronic acid in children with osteogenesis imperfecta and Bruck syndrome: a 2-year prospective observational study
Osteoporosis International ·Ghada A. Otaify, Mona Aglan, Mona Mohamed Ibrahim, Mostafa El-Nashar, Rokia AbdElshafy S. El Banna, Samia A. Temtamy
201530
19
Report of a newly indentified patient with mutations in BMP1 and underlying pathogenetic aspects
American Journal of Medical Genetics Part A ·(unknown), José A. Caparrós‐Martín, Ma Salomé Sirerol-Piquer, José Manuel García‐Verdugo, Víctor Martínez‐Glez, Pablo Lapunzina, Samia A. Temtamy, Mona Aglan, Allan M. Lund, Peter G. J. Nikkels, Víctor L. Ruiz‐Pérez, Elsebet Østergaard
201428
20
Adams–Oliver syndrome: further evidence of an autosomal recessive variant
Clinical Dysmorphology ·Samia A. Temtamy, Mona Aglan, Adel M. Ashour, Maha S. Zaki
200725

About Mona Aglan

Mona Aglan is a scholar working on Genetics, Molecular Biology, Rheumatology, Pediatrics, Perinatology and Child Health and Surgery, having authored 73 papers that have together received 1.7k indexed citations. Recurring topics across this work include Connective tissue disorders research (26 papers), Genomic variations and chromosomal abnormalities (9 papers), Bone and Dental Protein Studies (8 papers), Prenatal Screening and Diagnostics (6 papers), Congenital limb and hand anomalies (6 papers), Hedgehog Signaling Pathway Studies (6 papers), RNA modifications and cancer (6 papers) and Chromosomal and Genetic Variations (5 papers). The work is most often cited by research in Genetics (1.0k citations), Rheumatology (341 citations), Developmental Biology (53 citations), Molecular Biology (763 citations) and Cancer Research (142 citations). Mona Aglan has collaborated with scholars based in Egypt, United States and Spain. Frequent co-authors include Samia A. Temtamy, Víctor L. Ruiz‐Pérez, Pablo Lapunzina, José A. Caparrós‐Martín, Víctor Martínez‐Glez, Ghada A. Otaify, Khalda Amr, Adel M. Ashour, Maha S. Zaki and Verónica Pulido. Their work appears in journals such as Human Mutation, The American Journal of Human Genetics, Osteoporosis International, American Journal of Medical Genetics Part A and Archives of Oral Biology.

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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