Publications by authors named "Maleeha Maria"

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Alzheimer and cardiovascular genetic scores and cognition: the FINGER randomized controlled trial.
Gazi Saadmaan, Maria Carolina Dalmasso, Maleeha Maria, Jenni Lehtisalo, Mikko Hiltunen

Brain· August 2025

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Dissecting the polygenic basis of atherosclerosis via disease-associated cell state signatures.
Tiit Örd, Tapio Lönnberg, Valtteri Nurminen, Aarthi Ravindran, Henri Niskanen, Maleeha Maria

Am J Hum Genet· May 2023

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Late-onset and classic phenotypes of Fabry disease in males with the -Thr410Ala mutation.
Kati Valtola, Marja Hedman, Ilkka Kantola, Susanne Walls, Seppo Helisalmi, Maleeha Maria

Open Heart· March 2023

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Role of 19 SNPs in 10 genes with type 2 diabetes in the Pakistani population.
Netasha Khan, Andrew D Paterson, Delnaz Roshandel, Saadia Maqbool, Nosheen Fazal, Maleeha Maria

Gene· January 2023

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Metabolite Signature in the Carriers of Pathogenic Genetic Variants for Cardiomyopathy: A Population-Based METSIM Study.
Rowmika Ravi, Lilian Fernandes Silva, Jagadish Vangipurapu, Maleeha Maria, Joose Raivo

Metabolites· May 2022

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The Power of Single-Cell RNA Sequencing in eQTL Discovery.
Maleeha Maria, Negar Pouyanfar, Tiit Örd, Minna U Kaikkonen

Genes (Basel)· March 2022

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Cardiomyopathy associated with the Ala143Thr variant of the gene.
Kati Valtola, Juanita Nino-Quintero, Marja Hedman, Line Lottonen-Raikaslehto, Tomi Laitinen, Maleeha Maria

Heart· April 2020

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Clinical and Genetic Characterization of 153 Patients with Persistent or Transient Congenital Hyperinsulinism.
Jonna M E Männistö, Maleeha Maria, Joose Raivo, Teemu Kuulasmaa, Timo Otonkoski

J Clin Endocrinol Metab· April 2020

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Genetic and clinical characterization of Pakistani families with Bardet-Biedl syndrome extends the genetic and phenotypic spectrum.
Maleeha Maria, Ideke J C Lamers, Miriam Schmidts, Muhammad Ajmal, Sulman Jaffar

Sci Rep· October 2016

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Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistan.
Maleeha Maria, Muhammad Ajmal, Maleeha Azam, Nadia Khalida Waheed, Sorath Noorani Siddiqui

PLoS One· January 2016

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Screening of a large cohort of leber congenital amaurosis and retinitis pigmentosa patients identifies novel LCA5 mutations and new genotype-phenotype correlations.
Donna S Mackay, Arundhati Dev Borman, Ruifang Sui, L Ingeborgh van den Born, Eliot L Berson, Maleeha Maria

Hum Mutat· November 2013

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A nonsense mutation in S-antigen (p.Glu306*) causes Oguchi disease.
Nadia K Waheed, Ahmed H Qavi, Sarah N Malik, Maleeha Maria, Moeen Riaz

Mol Vis· December 2012

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