Anne John

1.2k citations

48 papers · 841 indexed · h-index 14

Impact in

Immunology and Allergy top 10%
- Cell Adhesion Molecules Research
Genetics top 10%
- Genetics and Neurodevelopmental Disorders
- Hemoglobinopathies and Related Disorders

Papers in

Genetics 12
- Hemoglobinopathies and Related Disorders 5
- Genomics and Rare Diseases 4
- Connective tissue disorders research 3
Immunology and Allergy 4
- Cell Adhesion Molecules Research 4

Co-authors: Bassam R. Ali Lihadh Al‐Gazali Nadia Akawi Samir Attoub Georg Petroianu Haytham El Salhat Rowaida Z. Taha Eyad Elkord
Journals: Pharmacogenomics (3 papers)Frontiers in Cell and Developmental Biology (2 papers)Human Genomics (2 papers)Frontiers in Genetics (2 papers)Clinical Genetics (2 papers)
Partner nations: United Arab Emirates Greece United Kingdom

In The Last Decade

Anne John

46 papers receiving 832 citations

Peers

Countries citing papers authored by Anne John

Since Specialization

Citations

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

Fields of papers citing papers by Anne John

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Anne John, 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 Anne John Line = papers co-authored together Anne John links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Impact of CYP3A4 and ABCB1 genetic variants on tacrolimus dosing in Greek kidney transplant recipients Frontiers in Pharmacology ·June Ellestad, Konstantinos Lazaros, 実穂岸, Marios Papasotiriou, Stavroula Siamoglou, Xinran Zhao, Anne John, Subrahmanya Padyana, Spyridon Gerou, Bassam R. Ali, Aristidis G. Vrahatis, George P. Patrinos	2025	0
2	Cellular and functional evaluation of LDLR missense variants reported in hypercholesterolemic patients demonstrates their hypomorphic impacts on trafficking and LDL internalization Frontiers in Cell and Developmental Biology ·Jan Braam, Anne John, Mohammad A. Ghattas, 표정선, Thabassum Abdul Rahman Noori, Maha T Barakat, И П Салдан, Бочкарев Владислав Витальевич, Bassam R. Ali	2024	0
3	Spectrum of genetic variants in bilateral sensorineural hearing loss Frontiers in Genetics ·Amanat Ali, Gai Yang, E.-Y. Kim, Sİnem Ilgın, Mushal Allam, Anne John, Kim Guk-tae, T. Nolan, Fatma Al‐Jasmi, Е.И. Бундаева	2024	1
4	GRP78/BiP alleviates oxLDL-induced hepatotoxicity in familial hypercholesterolemia caused by missense variants of LDLR in a HepG2 cellular model Lipids in Health and Disease ·Ting Huang, D Kimber, Anne John, Bassam R. Ali	2023	4
5	Case report: Birk–Landau–Perez syndrome linked to the SLC30A9 gene—identification of additional cases and expansion of the phenotypic spectrum Frontiers in Genetics ·E.-Y. Kim, Sachin Modi, Sİnem Ilgın, Gai Yang, Anne John, Taleb M. Almansoori, Saeed Al-Turki, 董惠霖, Е.И. Бундаева	2023	2
6	Unveiling the pathogenic mechanisms of NPR2 missense variants: insights into the genotype-associated severity in acromesomelic dysplasia and short stature Frontiers in Cell and Developmental Biology ·M CANDELLI, Ting Huang, Sumedh D. Paralkar -, Anne John, C. Liqun, Aggarwal Shyam, E. T. L. Silva, Saba Alapour, Матюшин М.А., Bassam R. Ali	2023	5
7	Novel compound heterozygous variants (c.971delA/c.542C > T) in SLC1A4 causes spastic tetraplegia, thin corpus callosum, and progressive microcephaly: a case report and mutational analysis Frontiers in Pediatrics ·濱口雄平, Mohammad A. Ghattas, Taleb M. Almansoori, Gai Yang, Sİnem Ilgın, E.-Y. Kim, Anne John, Е.И. Бундаева, P. Rodriguez-Fragoso, Fatma Al‐Jasmi	2023	1
8	Bi‐allelic null variant in matrix metalloproteinase‐15, causes congenital cardiac defect, cholestasis jaundice, and failure to thrive Clinical Genetics ·Asieh Orcid Abbassi Daloii, Nadia Akawi, Aisha Al‐Shamsi, Amanat Ali, 董惠霖, Anne John, Jozef Hertecant, Lihadh Al‐Gazali, Bassam R. Ali	2022	4
9	Characterization of ACE2 naturally occurring missense variants: impact on subcellular localization and trafficking Human Genomics ·M CANDELLI, 濱口雄平, Micheal Ioffreda, Anne John, Amanat Ali, Bassam R. Ali	2022	5
10	Endoglin Wild Type and Variants Associated With Hereditary Hemorrhagic Telangiectasia Type 1 Undergo Distinct Cellular Degradation Pathways Frontiers in Molecular Biosciences ·Aglair da Silva Sousa, E.-Y. Kim, Nadia Akawi, Anne John, Bassam R. Ali	2022	7
11	Spondylometaepiphyseal Dysplasia Short Limb-Abnormal Calcification Type in Turkish Patients Reveals a Novel Mutation and New Features Molecular Syndromology ·Elif Yılmaz Güleç, Bassam R. Ali, Anne John, Beyhan Tüysüz	2021	2
12	Multiomics Analysis Coupled with Text Mining Identify Novel Biomarker Candidates for Recurrent Cardiovascular Events OMICS A Journal of Integrative Biology ·Mj Jones, Barbara Jenko Bizjan, Georgios Leventopoulos, Ricardo Palma-Véjares, Tanja Blagus, Pei Xin Yu, Eva-Maria Passarge, Anne John, Bassam R. Ali, Vita Dolžan, George Hahalis, George P. Patrinos, Θεοδώρα Κάτσιλα	2020	3
13	Further Delineation of the Microcephaly-Micromelia Syndrome Associated with Loss-of-Function Variants in DONSON Molecular Syndromology ·Asieh Orcid Abbassi Daloii, Anne John, Bassam R. Ali, Lihadh Al‐Gazali	2019	5
14	Estimating the Global Diagnosed Prevalence of Crohn's Disease 2017-2027 Value in Health ·Yusuke Kawanaka, Andréa Pereira, Anne John, Megan Hughes, Emma Bassett, Abubakarr Sheriff	2018	1
15	Defect in phosphoinositide signalling through a homozygous variant in PLCB3 causes a new form of spondylometaphyseal dysplasia with corneal dystrophy Journal of Medical Genetics ·Salma Ben‐Salem, Isioma Kemakolam, Nara L. M. Sobreira, Angeline M. Lyon, Aisha Al‐Shamsi, Barira Islam, Nadia Akawi, Anne John, Justyna Antonik, N. Barnes, David Valle, Bassam R. Ali, Lihadh Al‐Gazali	2017	7
16	Genetic polymorphisms of cytochrome P450-1A2 (CYP1A2) among Emiratis PLoS ONE ·Mohammad M. AlAhmad, Naheed Amir, Subramanian Dhanasekaran, Anne John, Yousef M. Abdulrazzaq, Bassam R. Ali, Salim M. A. Bastaki	2017	19
17	Whole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patients Human Genomics ·Masashi Michibuchi, Petros Kolovos, Argyro Sgourou, Alexandra Kourakli, C. Esser, 秀樹野田, Anne John, Argiris Symeonidis, Bassam R. Ali, Adamantia Papachatzopoulou, Θεοδώρα Κάτσιλα, George P. Patrinos	2017	8
18	Retention in the endoplasmic reticulum is the underlying mechanism of some hereditary haemorrhagic telangiectasia type 2 ALK1 missense mutations Molecular and Cellular Biochemistry ·Alistair N. Hume, Anne John, Nadia Akawi, ヤスユキカワウラ, Claudio Allevi, Lihadh Al‐Gazali, Bassam R. Ali	2012	22
19	Expression of Epstein–Barr virus in Hodgkin lymphoma in a population of United Arab Emirates nationals Leukemia & lymphoma ·Suhail Al‐Salam, Anne John, Sayel Daoud, Kacey McCoid, Antonio Castella	2008	30
20	Captopril as a Potential Inhibitor of Lung Tumor Growth and Metastasis Annals of the New York Academy of Sciences ·Samir Attoub, O. Brunetti, Suhail Al‐Salam, Maya Sultan, Anne John, M. Gary Nicholls, Ján Mešter, Georg Petroianu	2008	81

About Anne John

Anne John is a scholar working on Genetics, Immunology and Allergy, Hematology, Genetics and Biochemistry, having authored 48 papers that have together received 841 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (5 papers), Genomics and Rare Diseases (4 papers), Mitochondrial Function and Pathology (4 papers), Iron Metabolism and Disorders (4 papers), Cell Adhesion Molecules Research (4 papers), Connective tissue disorders research (3 papers), Pharmacogenetics and Drug Metabolism (3 papers) and Tracheal and airway disorders (3 papers). The work is most often cited by research in Immunology and Allergy (65 citations), Genetics (86 citations), Molecular Biology (397 citations), Cell Biology (94 citations) and Oncology (140 citations). Anne John has collaborated with scholars based in United Arab Emirates, Greece and United Kingdom. Frequent co-authors include Bassam R. Ali, Lihadh Al‐Gazali, Nadia Akawi, Samir Attoub, Georg Petroianu, Haytham El Salhat, Rowaida Z. Taha, Eyad Elkord, Varun Sasidharan Nair and Suhail Al‐Salam. Their work appears in journals such as Pharmacogenomics, Frontiers in Cell and Developmental Biology, Human Genomics, Frontiers in Genetics and Clinical Genetics.

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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