Associated Papers
Genetic Variants Linked to Dyslexia Co-Morbid ADHD: A Case Study of a Pakistani Outpatient.
Haider S et al.
Journal of Population Therapeutics and Clinical Pharmacology = Journal De La Therapeutique Des Populations Et De La Pharmacologie Clinique, 2024
Peptide ancestry informative markers in uterine neoplasms from women of European, African, and Asian ancestry.
Bateman NW et al.
Iscience, 2022
35036865 (PubMed )
Supplement: mmc2.xlsx › SupplementalTable1A
Integrated Genomic, Functional, and Prognostic Characterization of Atypical Chronic Myeloid Leukemia.
Fontana D et al.
Hemasphere, 2020
33196013 (PubMed )
Supplement: hs9-4-e497-s006.xlsx › Sheet1
Treatment-associated TP53 DNA-binding domain missense mutations in the pathogenesis of secondary gliosarcoma.
Pain M et al.
Oncotarget, 2018
29416795 (PubMed )
Supplement: oncotarget-09-2603-s001.pdf
Doublecortin domain containing protein 2 (DCDC2) genetic variants in primary sclerosing cholangitis.
Cheung AC et al.
Journal of Hepatology, 2017
Reply to: "Doublecortin domain containing protein 2 (DCDC2) genetic variants in primary sclerosing cholangitis".
Grammatikopoulos T et al.
Journal of Hepatology, 2017
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Matsson H et al.
Journal of Human Genetics, 2015
Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.
Sun Y et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics, 2014
Analysis of genetic variants of dyslexia candidate genes KIAA0319 and DCDC2 in Indian population.
Venkatesh SK et al.
Journal of Human Genetics, 2013
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