Anne John

1.3k citations

50 papers · 1.1k · h-index 16

Impact in

Genetics top 10%
- Genomics and Rare Diseases
- Connective tissue disorders research
- Hemoglobinopathies and Related Disorders
Immunology and Allergy top 10%

Papers in

Genetics 19
- Genomics and Rare Diseases 12
- Connective tissue disorders research 8
- Genetics and Neurodevelopmental Disorders 5
- Hemoglobinopathies and Related Disorders 5
- Vascular Anomalies and Treatments 3
Pharmacology 4
- Pharmacogenetics and Drug Metabolism 4

Co-authors: Bassam R. Ali (39 shared papers)Lihadh Al‐Gazali (21 shared papers)Varun Sasidharan Nair (1 shared paper)Nadia A. Akawi (8 shared papers)Samir Attoub (2 shared papers)Eyad Elkord (1 shared paper)Haytham El Salhat (1 shared paper)Anne‐Marie Gaben (2 shared papers)
Journals: Human Genomics (4 papers)Clinical Genetics (3 papers)Pharmacogenomics (3 papers)Frontiers in Cell and Developmental Biology (2 papers)PLoS ONE (2 papers)
Partner nations: United Arab Emirates Greece United Kingdom

In The Last Decade

Anne John

50 papers receiving 1k 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-authors

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

Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Inhibition of cell survival, invasion, tumor growth and histone deacetylase activity by the dietary flavonoid luteolin in human epithelioid cancer cells European Journal of Pharmacology ·Samir Attoub, Ahmed H. Hassan, Barbara W.A. Vanhoecke, Rabah Iratni, Takashi Takahashi, Anne‐Marie Gaben, Marc Bracke, Salma Mahmoud Awad	2010	149
2	DNA methylation and repressive H3K9 and H3K27 trimethylation in the promoter regions of PD-1, CTLA-4, TIM-3, LAG-3, TIGIT, and PD-L1 genes in human primary breast cancer Clinical Epigenetics ·Varun Sasidharan Nair, Haytham El Salhat, Rowaida Ziad Taha, Anne John, Bassam R. Ali, Eyad Elkord	2018	127
3	Captopril as a Potential Inhibitor of Lung Tumor Growth and Metastasis Annals of the New York Academy of Sciences ·Samir Attoub, Anne‐Marie Gaben, Suhail Al‐Salam, Anne John, M. Gary Nicholls, Ján Mešter, Georg A. Petroianu +1 other	2008	84
4	Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patients Human Molecular Genetics ·Bassam R. Ali, Huifang Xu, Nadia A. Akawi, Anne John, Noushad S. Karuvantevida, Ruth D. Langer, Lihadh Al‐Gazali, Birgit Leitinger	2010	71
5	A Novel Whole Exon Deletion in WWOX Gene Causes Early Epilepsy, Intellectual Disability and Optic Atrophy Journal of Molecular Neuroscience ·Salma Ben‐Salem, Aisha M Al-Shamsi, Anne John, Bassam R. Ali, Lihadh Al‐Gazali	2014	42
6	Characterization of a peptide from skin secretions of male specimens of the frog, Leptodactylus fallax that stimulates aggression in male frogs Peptides ·Jay D. King, Louise A. Rollins‐Smith, Per Franklin Nielsen, Anne John, John Michael Conlon	2004	41
7	Associations of angiotensinogen gene mutations with hypertension and myocardial infarction in a gulf population Clinical Genetics ·Philippe M. Frossard, Susan H. Hill, Yassin I. Elshahat, E N Obineche, Awais Bokhari, Gilles G. Lestringant, Anne John, Abdishakur M Abdulle	1998	40
8	An MboI Two-Allele Polymorphism May Implicate the Human Renin Gene in Primary Hypertension. Hypertension Research ·Philippe M. Frossard, Gilles G. Lestringant, Yassin I. Elshahat, Anne John, E N Obineche	1998	36
9	Endoplasmic Reticulum Quality Control Is Involved in the Mechanism of Endoglin-Mediated Hereditary Haemorrhagic Telangiectasia PLoS ONE ·Bassam R. Ali, Imen Ben Rebeh, Anne John, Nadia A. Akawi, Reham M. Milhem, Nouf A. Al-Shehhi, Mouza Alameri, Shamma A. Al-Shamisi	2011	31
10	Expression of Epstein–Barr virus in Hodgkin lymphoma in a population of United Arab Emirates nationals Leukemia & lymphoma ·Suhail Al‐Salam, Anne John, Sayel A. Daoud, Siew Ming Chong, Antonio Castella	2008	29
11	A novel mutation in DDR2 causing spondylo-meta-epiphyseal dysplasia with short limbs and abnormal calcifications (SMED-SL) results in defective intra-cellular trafficking BMC Medical Genetics ·Adila Al‐Kindi, Praseetha Kizhakkedath, Huifang Xu, Anne John, Abeer Al‐Saegh, Anuradha Ganesh, Maha Al-Awadi, Lamya Al-Anbouri	2014	27
12	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 A. Akawi, Aydah M. Al-Awadhi, Sarah S. Al-Suwaidi, Lihadh Al‐Gazali, Bassam R. Ali	2012	22
13	Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients Human Genomics ·Konstantinos A. Mitropoulos, Eleni Merkouri Papadima, Georgia Xiromerisiou, Angeliki Balasopoulou, Kyriaki Charalampidou, Vasiliki Galani, Krystallia-Vassiliki Zafeiri, Efthimios Dardiotis	2017	22
14	Genetic polymorphisms of cytochrome P450-1A2 (CYP1A2) among Emiratis PLoS ONE ·Mohammad M. Al-Ahmad, Naheed Amir, Subramanian Dhanasekaran, Anne John, Yousef Mohamed Abdulrazzaq, Bassam R. Ali, Salim M. A. Bastaki	2017	22
15	Endoplasmic reticulum quality control of LDLR variants associated with familial hypercholesterolemia FEBS Open Bio ·Praseetha Kizhakkedath, Anne John, Buthaina K. Al‐Sawafi, Lihadh Al‐Gazali, Bassam R. Ali	2019	22
16	Defective cellular trafficking of the bone morphogenetic protein receptor type II by mutations underlying familial pulmonary arterial hypertension Gene ·Anne John, Praseetha Kizhakkedath, Lihadh Al‐Gazali, Bassam R. Ali	2015	21
17	Clinical and molecular delineation of dysequilibrium syndrome type 2 and profound sensorineural hearing loss in an inbred Arab family American Journal of Medical Genetics Part A ·Makanko Komara, Anne John, Jehan Suleiman, Bassam R. Ali, Lihadh Al‐Gazali	2015	16
18	A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvement Orphanet Journal of Rare Diseases ·Nadia A. Akawi, Salma Ben‐Salem, Jozef Hertecant, Anne John, Thachillath Pramathan, Praseetha Kizhakkedath, Bassam R. Ali, Lihadh Al‐Gazali	2016	16
19	A novel aberrant splice site mutation in COL27A1 is responsible for Steel syndrome and extension of the phenotype to include hearing loss American Journal of Medical Genetics Part A ·Nesrin Gariballa, Afif Ben‐Mahmoud, Makanko Komara, Aisha M Al-Shamsi, Anne John, Bassam R. Ali, Lihadh Al‐Gazali	2017	16
20	Correlation of SIN3A Genomic Variants with β-Hemoglobinopathies Disease Severity and Hydroxyurea Treatment Efficacy Pharmacogenomics ·Aikaterini Gravia, Vasiliki Chondrou, Αλεξάνδρα Κολλιοπούλου, Alexandra Kourakli, Anne John, Argiris S. Symeonidis, Bassam R. Ali, Argyro Sgourou	2016	15

About Anne John

Anne John is a scholar working on Genetics, Genetics, Pharmacology, Cell Biology and Clinical Biochemistry, having authored 50 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Connective tissue disorders research (8 papers), Genetics and Neurodevelopmental Disorders (5 papers), Hemoglobinopathies and Related Disorders (5 papers), Pharmacogenetics and Drug Metabolism (4 papers), Renin-Angiotensin System Studies (4 papers), Endoplasmic Reticulum Stress and Disease (3 papers) and Vascular Anomalies and Treatments (3 papers). The work is most often cited by research in Genetics (70 citations), Genetics (166 citations), Immunology and Allergy (26 citations), Oncology (113 citations) and Cardiology and Cardiovascular Medicine (116 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, Varun Sasidharan Nair, Nadia A. Akawi, Samir Attoub, Eyad Elkord, Haytham El Salhat, Anne‐Marie Gaben, Rowaida Ziad Taha and Georg A. Petroianu. Their work appears in journals such as Human Genomics, Clinical Genetics, Pharmacogenomics, Frontiers in Cell and Developmental Biology and PLoS ONE.

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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