Shariq Ahmed
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Explore the profile of Shariq Ahmed including associated specialties, affiliations and a list of published articles.
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21
Citations
65
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Recent Articles
1.
Liu R, Song Y, Hua R, Ahmed S, Xie Y, Lai C, et al.
Phenomics
. 2024 Nov;
4(4):339-351.
PMID: 39583313
Supplementary Information: The online version contains supplementary material available at 10.1007/s43657-024-00160-2.
2.
Fatima N, Ahmed S, Shameem M, Ahmed A, Hasan W, Khan P
Indian J Med Microbiol
. 2023 Aug;
46:100467.
PMID: 37651764
Objective: An unprecedented rise in mucormycosis cases; apparently called 'an epidemic within a pandemic' was seen worldwide. Therefore, the following study was conducted to know the epidemiology, underlying risk factors,...
3.
Siddiqi M, Boeckelmann D, Naz A, Imran A, Ahmed S, Najmuddin A, et al.
Cells
. 2023 Jan;
12(2).
PMID: 36672149
Glanzmann thrombasthenia (GT) is a rare autosomal recessive inherited platelet disorder occurring frequently in populations with high incidence of consanguineous marriages. GT is characterized by quantitative and/or qualitative defect of...
4.
Mukry S, Ahmed S, Bukhari A, Shahni A, Sufaida G, Naz A, et al.
J Infect Dev Ctries
. 2021 Nov;
15(10):1376-1383.
PMID: 34780358
Introduction: The first case of severe acute respiratory syndrome 2 (SARS-CoV-2) was imported to Pakistan in February 2020, since then 8,260 deaths have been witnessed. The virus has been constantly...
5.
Yadegari H, Biswas A, Ahmed S, Naz A, Oldenburg J
Hum Mutat
. 2021 May;
42(6):731-744.
PMID: 33942438
von Willebrand disease (VWD), the most prevalent congenital bleeding disorder, arises from a deficiency in von Willebrand factor (VWF), which has crucial roles in hemostasis. The present study investigated functional...
6.
Shahid S, Shakeel M, Siddiqui S, Ahmed S, Sohail M, Khan I, et al.
Front Genet
. 2020 Jul;
11:560.
PMID: 32655615
Acute myeloid leukemia (AML) is a hematological malignancy characterized by clonal expansion of blast cells that exhibit great genetic heterogeneity. In this study, we describe the mutational landscape and its...
7.
Ahmed S, Yadegari H, Naz A, Biswas A, Budde U, Saqlain N, et al.
Haemophilia
. 2019 Sep;
25(6):1035-1044.
PMID: 31532876
Introduction: Type 3 von Willebrand disease (VWD), a severe autosomal recessive hereditary bleeding disorder, is described by the virtual absence of von Willebrand factor (VWF). In consanguineous populations, for example...
8.
Hassan J, Nadeem M, Ansari S, Ahmed S, Parveen S, Shamsi T
J Pak Med Assoc
. 2019 Jul;
69(7):959-963.
PMID: 31308562
Objective: To find frequency ofalpha Thalsaemia nhomozygous beta Thalsaemia patients, and to se any difernce infrequency and age ofirst ransfusion and mean haemoglobin concentration. Methods: The single-centred, escriptive cros-sectional study...
9.
Shahid S, Zaidi S, Ahmed S, Siddiqui S, Abid A, Malik S, et al.
Front Genet
. 2019 May;
10:360.
PMID: 31068971
Leukocyte adhesion deficiency-III (LAD3) is an extremely rare primary immunodeficiency disorder, transmitted with autosomal-recessive inheritance. It is caused by genetic alteration in the gene, which leads to abnormal expression of...
10.
Naz A, Biswas A, Khan T, Goodeve A, Ahmed N, Saqlain N, et al.
Thromb J
. 2019 Apr;
17:5.
PMID: 30988665
[This corrects the article DOI: 10.1186/s12959-017-0143-3.].