ArticleGenes2026
Complexity of Inheritance of Pathogenic Mutations Associated with Epilepsy in Consanguine Families from Pakistan.
Khajista Tahira, Anwar Ullah, Fazl Ullah, Jeena Aziz, Muhammad Ishaq Javed, Aasma Kiyani, Azra Khanum, Kerstin Hallmann, Tobias Baumgartner, Rainer Surges and 2 more
Abstract read
In one paragraphArticle in Genes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
2 · The registryThe trial behind it
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3 · Its place in the literatureWho cites it
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4 · The recordCorrections and comments
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5 · Who and what moneyAuthors and funding
12 authors.
Khajista TahiraDepartment of Epileptology, University Bonn Medical Center, 53127 Bonn, Germany.
Anwar UllahInstitute of Paramedical Sciences, Khyber Medical University Peshawar, Peshawar 25100, Pakistan.ORCID 0000-0002-3461-1518 Fazl UllahDistrict Headquarters (DHQ) Hospital Alpuri Shangla, Alpuri 19100, Pakistan.
Jeena AzizInstitute of Paramedical Sciences, Khyber Medical University Peshawar, Peshawar 25100, Pakistan.
Muhammad Ishaq JavedUniversity Institute of Biochemistry and Biotechnology, PMAS Arid Agriculture University Rawalpindi, Rawalpindi 46000, Pakistan.ORCID 0000-0002-0831-2426 Aasma KiyaniNational Institute of Rehabilitation Medicine, Islamabad 44000, Pakistan.
Azra KhanumUniversity Institute of Biochemistry and Biotechnology, PMAS Arid Agriculture University Rawalpindi, Rawalpindi 46000, Pakistan.
Kerstin HallmannInstitute of Experimental Epileptology and Cognition Research, University Bonn, 53127 Bonn, Germany.
Tobias BaumgartnerDepartment of Epileptology, University Bonn Medical Center, 53127 Bonn, Germany.
Pakeeza Arzoo ShaiqUniversity Institute of Biochemistry and Biotechnology, PMAS Arid Agriculture University Rawalpindi, Rawalpindi 46000, Pakistan.ORCID 0000-0003-0952-5375 Funding
International Research Support Initiative Program (IRSIP) No:1-8\HEC\HRD\2025\51693, date of approval 21/02/2025Pakistan Academy of Sciences PAS/PSDP#302, date of approval 10/05/2024
6 · The paper itselfAbstract
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Indexed as
ConsanguinityEpilepsyMutationChildExome SequencingFemaleGenes, RecessiveHumansMalePakistanPedigreeconsanguine familiesinheritance of pathogenic mutationsrecessive epilepsy genes
Identifiers
PMID41751541
PMCPMC12940928
What OpenQuestion holds
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