Publications by authors named "Safdar Abbas"

Claim this Profile
D
Dual-Functional Phosphorus-Doped Iron Single-Atom Catalyst on Reduced Graphene Oxide for Efficient Lithium-Sulfur Batteries: Simultaneous Polysulfides Trapping/Catalysis and Lithium Deposition Regulation.
Abdul Hameed Pato, Longtao Ren, Imran Ali Chandio, Qiaoli Zhang, Yizhe Li, Safdar Abbas

Small· August 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Self-assembly of ruthenium-doped oxygen-deficient tungsten oxide as an efficient electrocatalyst for the hydrogen evolution reaction in acidic environments.
Elhussein Desoki Helal, Wenhai Xu, Yizhe Li, Liyao Gao, Hao Sun, Safdar Abbas

Chem Commun (Camb)· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prevalence and chemotherapy of Staphylococcus aureus mastitis in dairy cattle.
Asjad Umair Shah, Jawaria Ali Khan, Muhammad Avais, Syed Haider Zaman, Zubir Munir, Safdar Abbas

PLoS One· May 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Modulation of plant growth and development through altered ethylene binding affinity of the ethylene receptor ETR1.
Sitwat Aman, Swadhin Swain, Esha Dutta, Safdar Abbas, Ning Li

BMC Plant Biol· April 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A Novel Homozygous Loss-of-Function Variant in GPR156 Delineates Non-syndromic Hearing Loss.
M Muaaz Aslam, Safdar Abbas, Shoaib Nawaz, Gohar Zaman, Ishtiaq Ahmed

Biochem Genet· January 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Truncated SPAG9 as a novel candidate gene for a new syndrome: Coarse facial features, albinism, cataract and developmental delay (CACD syndrome).
Majid Alfadhel, Bashayr S Alhubayshi, Muhammad Umair, Ahmed Alfaidi, Deemah Alwadaani, Safdar Abbas

Genet Mol Biol· January 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Biallelic loss-of-function variant causes intellectual disability, developmental delay, and dysmorphic features.
Fuad Al Mutairi, Faisal Joueidi, Maha Alshalan, Essra Aloyouni, Mariam Ballow, Safdar Abbas

Heliyon· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The genetic cause of neurodevelopmental disorders in 30 consanguineous families.
Sohail Aziz Paracha, Shoaib Nawaz, Muhammad Tahir Sarwar, Asmat Shaheen, Gohar Zaman, Safdar Abbas

Front Med (Lausanne)· August 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Stability Analysis of SARS-CoV-2 with Heart Attack Effected Patients and Bifurcation.
Aqeel Ahmad, Safdar Abbas, Mustafa Inc, Abdul Ghaffar

Adv Biol (Weinh)· April 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss-of-function variant in the LRR domain of SLITRK2 implicated in a neurodevelopmental disorder.
Tayyaba Afsar, Hongxia Fu, Hammal Khan, Zain Ali, Zamrud Zehri, Safdar Abbas

Front Genet· January 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
O
Overlapping neurological phenotypes in two extended consanguineous families with novel variants in the CNTNAP1 and ADGRG1 genes.
Shazia Khan, Muhammad Umair, Safdar Abbas, Uroba Ali, Gohar Zaman

J Gene Med· October 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Analysis of a non-lethal biallelic frameshift mutation in ZMPSTE24 reveals utilization of alternative translation initiation codons.
Lukas Kaufmann, Johannes Pilic, Lisa Auinger, Anna-Lena Mayer, Jasmin Blatterer, Safdar Abbas

Clin Genet· October 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
Truncated DNM1 variant underlines developmental delay and epileptic encephalopathy.
Tayyaba Afsar, Xiaoyun Huang, Abid Ali Shah, Safdar Abbas, Shazia Bano

Front Pediatr· October 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
AMFR dysfunction causes autosomal recessive spastic paraplegia in human that is amenable to statin treatment in a preclinical model.
Ruizhi Deng, Eva Medico-Salsench, Anita Nikoncuk, Reshmi Ramakrishnan, Kristina Lanko, Safdar Abbas

Acta Neuropathol· August 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel de novo variant in the PHF21A causes craniofacial abnormalities, intellectual disability and skeletal manifestations.
Sumayya Mustafa, Safdar Abbas, Arif Mahmood, Ali Zaman Khan, Shah Zeb

Clin Genet· July 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
Basis for high-affinity ethylene binding by the ethylene receptor ETR1 of Arabidopsis.
Beenish J Azhar, Safdar Abbas, Sitwat Aman, Maria V Yamburenko, Wei Chen

Proc Natl Acad Sci U S A· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel homozygous truncating variant in PPFIBP1 further delineates PPFIBP1-associated neurodevelopmental disorder.
Ahmed Waqas, Romana Liaqat, Sidrah Shaheen, Ali Zaman Khan, Mujahid, Safdar Abbas

Int J Dev Neurosci· April 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A GHRHR founder mutation causes isolated growth hormone deficiency type IV in a consanguineous Pakistani family.
Safeer Ahmad, Muhammad Zeeshan Ali, Sumra Wajid Abbasi, Safdar Abbas, Iftikhar Ahmed, Shakil Abbas

Front Endocrinol (Lausanne)· March 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Family capital, social stratification, and access to higher education: An empirical study in mainland China.
Qinyi Tan, Chencheng Li, Pei Wu, Safdar Abbas, Luyan Teng

Front Psychol· January 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles.
Khalid Al Hawsawi, Mazin Al Jabri, Mazen S Dajam, Bashaer Almahdi, Waseem K Alhawsawi, Safdar Abbas

Front Genet· August 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Syngas analysis by hybrid modeling of sewage sludge gasification in downdraft reactor: Validation and optimization.
Karthickeyan Viswanathan, Safdar Abbas, Wei Wu

Waste Manag· May 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability.
Ahmed Waqas, Anam Nayab, Shabnam Shaheen, Safdar Abbas, Muhammad Latif

Front Genet· April 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Hepatoprotective Screening of (Qazilb.) Y.R. Ling.
Maroof Ali, Hidayat Hussain, Amjad Hussain, Abdur Rauf, Wahid Hussain, Safdar Abbas

Biomed Res Int· January 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures.
Beryl Royer-Bertrand, Marine Jequier Gygax, Katarina Cisarova, Jill A Rosenfeld, Jennifer A Bassetti, Safdar Abbas

Mol Autism· October 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
D
Determinants of women's empowerment in Pakistan: evidence from Demographic and Health Surveys, 2012-13 and 2017-18.
Safdar Abbas, Noman Isaac, Munir Zia, Rubeena Zakar, Florian Fischer

BMC Public Health· July 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis