Mahmoud E Koko (Mahmoud Koko)

Scopus Author ID Loop profile ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 10

Top Venues

European journal of human genetics : EJHG

medRxiv : the preprint server for health sciences

Epilepsia

Cerebral cortex (New York, N.Y. : 1991)

Eberhard Karls Universität Tübingen Hertie Institut für klinische Hirnforschung (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Eberhard Karls Universität Tübingen Hertie Institut für klinische Hirnforschung Oct 01 2016

Germany

PHD :: Experimental Epileptology

University of Khartoum Sep 15 2012 - Sep 01 2014

Sudan

MSC

University of Khartoum Oct 01 2005 - Jan 03 2012

Sudan

BSC

Publications

Mahmoud E Koko, F Kyle Satterstrom, null null, null null, Varun Warrier, Hilary C Martin
Contribution of autosomal rare and de novo variants to sex differences in autism. medRxiv : the preprint server for health sciences (2024)
Mahmoud E Koko, F Kyle Satterstrom, null null, null null, Varun Warrier, Hilary C Martin
Contribution of autosomal rare and de novo variants to sex differences in autism. medRxiv : the preprint server for health sciences (2024)
Mahmoud E Koko, Maha A Elseed, Inaam N Mohammed, Ahlam A Hamed, Amal S I Abd Allah, Ashraf Yahia, Rayan A Siddig, Janine Altmüller, Mohammad Reza Toliat, Esra O Elmahdi, Mutaz Amin, Elhami A Ahmed, Isra Z M Eltazi, Fatima A Elmugadam, Wasma A Abdelgadir, Esraa Eltaraifee, Mohamed O M Ibrahim, Nabila M H Ali, Hiba M Malik, Arwa M Babai, Yousuf H Bakhit, Peter Nürnberg, Muntaser E Ibrahim, Mustafa A Salih, Julian Schubert, Liena E O Elsayed, Holger Lerche
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy. European journal of human genetics : EJHG (2024)
Mahmoud E Koko, F Kyle Satterstrom, null null, null null, Varun Warrier, Hilary C Martin
Contribution of autosomal rare and de novo variants to sex differences in autism. medRxiv : the preprint server for health sciences (2024)
Sandra Martins, Ashraf Yahia, Inês P D Costa, Hassab E Siddig, Rayan Abubaker, Mahmoud E Koko, Marc Corral-Juan, Antoni Matilla-Dueñas, Alexis Brice, Alexandra Dürr, Eric Leguern, Laura P W Ranum, Antonio Amorim, Liena E O Elsayed, Giovanni Stevanin, Leonor Correia Guedes
Machado-Joseph disease in a Sudanese family links East Africa to Portuguese families and allows reestimation of ancestral age of the Machado lineage. Human genetics (2023)
Ashraf Yahia, Ahlam A A Hamed, Inaam N Mohamed, Maha A Elseed, Mustafa A Salih, Sarah M El-Sadig, Hassab Elrasoul Siddig, Ali Elsir Musa Nasreldien, Mohamed Ahmed Abdullah, Maha Elzubair, Farouk Yassen Omer, Aisha Motwakil Bakhiet, Rayan Abubaker, Fatima Abozar, Rawaa Adil, Sara Emad, Mhammed Alhassan Musallam, Isra Z M Eltazi, Zulfa Omer, Hiba Malik, Mayada O E Mohamed, Ali A Elhassan, Eman O E Mohamed, Ahmed K M A Ahmed, Elhami A A Ahmed, Esraa Eltaraifee, Bidour K Hussein, Amal S I Abd Allah, Lina Salah, Mohammed Nimir, Omnia M Tag Elseed, Tasneem E A Elhassan, Abubakr Elbashier, Esraa S A Alfadul, Moneeb Fadul, Khalil F Ali, Shaimaa Omer M A Taha, Elfatih E Bushara, Mutaz Amin, Mahmoud E Koko, Muntaser E Ibrahim, Ammar E Ahmed, Liena E O Elsayed, Giovanni Stevanin
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations. European journal of human genetics : EJHG (2023)
Mohammed O E Abdallah, Mahmoud E Koko, Raj Ramesar
Lost in translation: the pitfalls of ensembl gene annotations between human genome assemblies and their impact on diagnostics. Expert review of molecular diagnostics (2023)
Ellen Knierim, Johannes Vogt, Michael Kintscher, Alexey Ponomarenko, Jan Baumgart, Prateep Beed, Tatiana Korotkova, Thorsten Trimbuch, Axel Panzer, Ortrud K Steinlein, Ulrich Stephani, Andrew Escayg, Mahmoud E Koko, Yuanyuan Liu, Holger Lerche, Dietmar Schmitz, Robert Nitsch, Markus Schuelke
Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype. Cerebral cortex (New York, N.Y. : 1991) (2023)
Mahmoud E Koko, Joshua E Motelow, Kate E Stanley, Dheeraj Reddy Bobbili, Ryan S Dhindsa, Patrick May, null null, null null, null null, null null, null null
Association of ultra-rare coding variants with genetic generalized epilepsy: A case-control whole exome sequencing study. Epilepsia 63 (3) (2022)
Liena E O Elsayed, Inaam N Mohammed, Ahlam A A Hamed, Maha A Elseed, Adam Johnson, Mathilde Mairey, Hassab Elrasoul S A Mohamed, Mohamed N Idris, Mustafa A M Salih, Sarah M El-Sadig, Mahmoud E Koko, Ashraf Y O Mohamed, Laure Raymond, Marie Coutelier, Frédéric Darios, Rayan A Siddig, Ahmed K M A Ahmed, Arwa M A Babai, Hiba M O Malik, Zulfa M B M Omer, Eman O E Mohamed, Hanan B Eltahir, Nasr Aldin A Magboul, Elfatih E Bushara, Abdelrahman Elnour, Salah M Abdel Rahim, Abdelmoneim Alattaya, Mustafa I Elbashir, Muntaser E Ibrahim, Alexandra Durr, Anjon Audhya, Alexis Brice, Ammar E Ahmed, Giovanni Stevanin
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan. European journal of human genetics : EJHG 25 (1) (2016)

Mahmoud E Koko (Mahmoud Koko)

Publication Activity (10 Years)

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