Mohammed Uddin

13.0k citations

70 papers · 1.5k indexed · h-index 23

Impact in

Health Informatics top 5%
Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases

Papers in ⓘ

Genetics 29
- Genetics and Neurodevelopmental Disorders 16
- Genomic variations and chromosomal abnormalities 13
- Genomics and Rare Diseases 12
Molecular Biology 27
- Congenital heart defects research 5

Co-authors: Marc Woodbury‐Smith (14 shared papers)Yujiang Wang (1 shared paper)Stephen W. Scherer (17 shared papers)Alawi Alsheikh‐Ali (13 shared papers)Tom Loney (5 shared papers)Norbert Nowotny (4 shared papers)Hanan Al Suwaidi (4 shared papers)Abiola Senok (4 shared papers)
Journals: Scientific Reports (5 papers)Molecular Autism (3 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2 papers)Nature Genetics (2 papers)Journal of Neurodevelopmental Disorders (2 papers)
Partner nations: United Arab Emirates Canada United Kingdom

In The Last Decade

Mohammed Uddin

62 papers receiving 1.5k citations

Peers

Countries citing papers authored by Mohammed Uddin

Since Specialization

Citations

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

Fields of papers citing papers by Mohammed Uddin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mohammed Uddin, 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 Mohammed Uddin Line = papers co-authored together Mohammed Uddin 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 70 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	SARS-CoV-2/COVID-19: Viral Genomics, Epidemiology, Vaccines, and Therapeutic Interventions Viruses ·Mohammed Uddin, Farah Mustafa, Tahir A. Rizvi, Tom Loney, Hanan Al Suwaidi, Ahmed H. Hassan Al-Marzouqi, Afaf Kamal Eldin, Nabeel H. M. Alsabeeha, Thomas E. Adrian, Cesare Stefanini, Norbert Nowotny, Alawi Alsheikh‐Ali, Abiola Senok	2020	198
2	Artificial intelligence for precision medicine in neurodevelopmental disorders npj Digital Medicine ·Mohammed Uddin, Yujiang Wang, Marc Woodbury‐Smith	2019	135
3	Sonic hedgehog (Shh) signaling promotes tumorigenicity and stemness via activation of epithelial-to-mesenchymal transition (EMT) in bladder cancer Molecular Carcinogenesis ·Syed S. Islam, Reza Bayat Mokhtari, Abu Shadat Mohammod Noman, Mohammed Uddin, M Z Rahman, Mohammad Ali Azadi, Alexandre R. Zlotta, Theodorus van der Kwast, Herman Yeger, Walid A. Farhat	2015	111
4	Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder Nature Genetics ·Mohammed Uddin, Kristiina Tammimies, Giovanna Pellecchia, Babak Alipanahi, Pingzhao Hu, Zhuozhi Wang, Dalila Pinto, Lynette Lau, Thomas Nalpathamkalam, Christian R. Marshall, Benjamin J. Blencowe, Brendan J. Frey, Daniele Merico, Ryan K. C. Yuen, Stephen W. Scherer	2014	98
5	Tissue engineering the retinal ganglion cell nerve fiber layer Biomaterials ·Karl E. Kador, Ramon B. Montero, Praseeda Venugopalan, Jonathan Hertz, Allison N. Zindell, Daniel A. Valenzuela, Mohammed Uddin, Erin Lavik, Kenneth J. Muller, Fotios M. Andreopoulos, Jeffrey L. Goldberg	2013	62
6	Host transcriptomic profiling of COVID-19 patients with mild, moderate, and severe clinical outcomes Computational and Structural Biotechnology Journal ·Ruchi Jain, Sathishkumar Ramaswamy, Divinlal Harilal, Mohammed Uddin, Tom Loney, Norbert Nowotny, Hanan Al Suwaidi, Rupa Varghese, Zulfa Deesi, Abdulmajeed Alkhajeh, Hamda Khansaheb, Alawi Alsheikh‐Ali, Ahmad Abou Tayoun	2020	55
7	Overexpression of sonic hedgehog in the triple negative breast cancer: clinicopathological characteristics of high burden breast cancer patients from Bangladesh Scientific Reports ·Abu Shadat Mohammod Noman, Mohammed Uddin, Md. Zillur Rahman, Mohammad Nayeem, Sharmin Alam, Zehedina Khatun, Md Wahiduzzaman, Afrin Sultana, Md Lutfur Rahman, M. Y. Ali, Dipta Barua, Imtiaz Ahmed, M. S. Islam, Abdelilah Aboussekhra, Herman Yeger, Walid A. Farhat, Syed S. Islam	2016	54
8	ARTS1 polymorphisms are associated with ankylosing spondylitis in Koreans Annals of the Rheumatic Diseases ·Chan‐Bum Choi, Tae‐Hwan Kim, Jae‐Bum Jun, Hye‐Soon Lee, Seung Cheol Shim, Bitnara Lee, Autumn N. Pope, Mohammed Uddin, Proton Rahman, Robert D. Inman	2009	54
9	Uncovering obsessive-compulsive disorder risk genes in a pediatric cohort by high-resolution analysis of copy number variation Journal of Neurodevelopmental Disorders ·Matthew J. Gazzellone, Mehdi Zarrei, Christie L. Burton, Susan Walker, Mohammed Uddin, S.‐M. Shaheen, Julie Coste, Rageen Rajendram, Reva Schachter, Marlena Colasanto, Gregory L. Hanna, David R. Rosenberg, Noam Soreni, Kate D. Fitzgerald, Christian R. Marshall, Janet A. Buchanan, Daniele Merico, Paul Arnold, Stephen W. Scherer	2016	49
10	Copy number variation in Han Chinese individuals with autism spectrum disorder Journal of Neurodevelopmental Disorders ·Matthew J. Gazzellone, Xue Zhou, Anath C. Lionel, Mohammed Uddin, Bhooma Thiruvahindrapuram, Shuang Liang, Caihong Sun, Jia Wang, Mingyang Zou, Kristiina Tammimies, Susan Walker, Thanuja Selvanayagam, John Wei, Zhuozhi Wang, Lijie Wu, Stephen W. Scherer	2014	44
11	Meta‐analysis and candidate gene mining of low‐phosphorus tolerance in maize Journal of Integrative Plant Biology ·Hongwei Zhang, Mohammed Uddin, Cheng Zou, Chuanxiao Xie, Yunbi Xu, Wenxue Li	2014	42
12	Salivary lysozyme: A noninvasive marker for the study of the effects of stress on natural immunity International Journal of Behavioral Medicine ·Shantha Perera, Mohammed Uddin, Julie Hayes	1997	41
13	Germline and somatic mutations in STXBP1 with diverse neurodevelopmental phenotypes Neurology Genetics ·Mohammed Uddin, Marc Woodbury‐Smith, Ada J. S. Chan, Ledia Brunga, Sylvia Lamoureux, Giovanna Pellecchia, Ryan K. C. Yuen, Muhammad Faheem, Dimitri J. Stavropoulos, James M. Drake, Cecil D. Hahn, Cynthia Hawkins, Adam Shlien, Christian R. Marshall, Lesley Turner, Berge A. Minassian, Stephen W. Scherer, Cyrus Boelman	2017	35
14	Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly Molecular Autism ·Marc Woodbury‐Smith, Éric Deneault, Ryan K. C. Yuen, Susan Walker, Mehdi Zarrei, Giovanna Pellecchia, Jennifer Howe, Ny Hoang, Mohammed Uddin, Christian R. Marshall, Christina Chrysler, Ann Thompson, Péter Szatmári, Stephen W. Scherer	2017	33
15	The clinical presentation of avoidant restrictive food intake disorder in children and adolescents is largely independent of sex, autism spectrum disorder and anxiety traits EClinicalMedicine ·Rosie Watts, Tanith Archibald, Pippa Hembry, Maxine Howard, Cate Kelly, Rachel Loomes, Laura Markham, Harry Moss, Alfonce Munuve, Anca Oros, Amy Siddall, Charlotte Rhind, Mohammed Uddin, Zain Ahmad, Rachel Bryant‐Waugh, Christopher Hübel	2023	30
16	Expanding the neurodevelopmental phenotypes of individuals with de novo KMT2A variants npj Genomic Medicine ·Ada J. S. Chan, Cheryl Cytrynbaum, Ny Hoang, Patricia Ambrozewicz, Rosanna Weksberg, Irene Drmic, Anne M. Ritzema, Russell Schachar, Susan Walker, Mohammed Uddin, Mehdi Zarrei, Ryan K. C. Yuen, Stephen W. Scherer	2019	29
17	Antibody-drug conjugate T-DM1 treatment for HER2+ breast cancer induces ROR1 and confers resistance through activation of Hippo transcriptional coactivator YAP1 EBioMedicine ·Syed S. Islam, Mohammed Uddin, Abu Shadat Mohammod Noman, Hosneara Akter, Nusrat J. Dity, Mohammad Basiruzzman, K. M. Furkan Uddin, Jahanara Ahsan, Sunera Annoor, Ayodele Alaiya, Monther Al‐Alwan, Herman Yeger, Walid A. Farhat	2019	29
18	Variable phenotype expression in a family segregating microdeletions of the NRXN1 and MBD5 autism spectrum disorder susceptibility genes npj Genomic Medicine ·Marc Woodbury‐Smith, Rob Nicolson, Mehdi Zarrei, Ryan K. C. Yuen, Susan Walker, Jennifer Howe, Mohammed Uddin, Ny Hoang, Janet A. Buchanan, Christina Chrysler, Ann Thompson, Péter Szatmári, Stephen W. Scherer	2017	29
19	SARS-CoV-2 may hijack GPCR signaling pathways to dysregulate lung ion and fluid transport American Journal of Physiology-Lung Cellular and Molecular Physiology ·Reem Abdel Hameid, Estelle Cormet‐Boyaka, Wolfgang M. Kuebler, Mohammed Uddin, Bakhrom K. Berdiev	2021	29
20	De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: A case report and a brief literature review American Journal of Medical Genetics Part A ·Yi Liu, Dongmei Zhao, Rui Dong, Xiaomeng Yang, Yanqing Zhang, Kristiina Tammimies, Mohammed Uddin, Stephen W. Scherer, Zhongtao Gai	2015	26

About Mohammed Uddin

Mohammed Uddin is a scholar working on Genetics, Molecular Biology, Cognitive Neuroscience, Infectious Diseases and Rheumatology, having authored 70 papers that have together received 1.5k indexed citations. Recurring topics across this work include Autism Spectrum Disorder Research (16 papers), Genetics and Neurodevelopmental Disorders (16 papers), Genomic variations and chromosomal abnormalities (13 papers), Genomics and Rare Diseases (12 papers), SARS-CoV-2 and COVID-19 Research (7 papers), Congenital heart defects research (5 papers), Spondyloarthritis Studies and Treatments (5 papers) and COVID-19 Clinical Research Studies (5 papers). The work is most often cited by research in Health Informatics (30 citations), Genetics (415 citations), Infectious Diseases (231 citations), Cognitive Neuroscience (200 citations) and Molecular Biology (619 citations). Mohammed Uddin has collaborated with scholars based in United Arab Emirates, Canada and United Kingdom. Frequent co-authors include Marc Woodbury‐Smith, Yujiang Wang, Stephen W. Scherer, Alawi Alsheikh‐Ali, Tom Loney, Norbert Nowotny, Hanan Al Suwaidi, Abiola Senok, Proton Rahman and Herman Yeger. Their work appears in journals such as Scientific Reports, Molecular Autism, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Nature Genetics and Journal of Neurodevelopmental Disorders.

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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