Gillian Riordan - Publications, H-index & Citations

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Gillian Riordan

University of Cape Town

10H-index

30Paper Count

294Citation Count

Published Papers 8

Publication Date

Acrodynia in a child due to household mercury exposure: a case report

Toxicology Communications

IF0.5

2025-12-31

OAAI

Mabala, T.; Stephen, C. R.; Ndondo, A. P.; Riordan, G.; Hlela, C.

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Hearing rehabilitation in SERAC1 related MEGD(H)EL syndrome – implications from a multi-center retrospective cohort study

Molecular Genetics and Metabolism

IF3.5

2025-07-21

OAAI

Sebastian Roesch; Anna O'Sullivan; Stefan Tschani; Anna Baghdasaryan; Shanti Balasubramaniam; Ivo Barić; Lonneke de Boer; Sarah C. Grünert; Anna Guzek; Mirian Janssen; Zita Krumina; Mary Kay Koenig; Ashleigh M. Lewkowitz; Fanny Mochel; Arianne Monge Naldi; Barbara Plecko; Kerem Öztürk; Lauren O'Grady; Gillian Riordan; Daisy Rymen; Inderneel Sahai; René Santer; Manuel Schiff; Georg M. Stettner; Konstantinos Tsiakas; Sema Kalkan Uçar; Özlem Ünal Uzun; Corina Weigel; Peter Witters; Kajus Merkevicius; Johannes A. Mayr; Saskia B. Wortmann; Katarzyna Iwanicka-Pronicka

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EPILEPSIA

IF6.6

2024-01-17

PREAI

Yoganathan, Sangeetha; Whitney, Robyn; Thomas, Maya; Danda, Sumita; Chettali, Akbar Mohamed; Prasad, Asuri N.; Farhan, Sali M. K.; Alsowat, Daad; Abukhaled, Musaad; Aldhalaan, Hesham; Gowda, Vykuntaraju K.; Kinhal, Uddhava V.; Bylappa, Arun Y.; Konanki, Ramesh; Lingappa, Lokesh; Parchuri, Bindu Madhavi; Appendino, Juan P.; Scantlebury, Morris H.; Cunningham, Jessie; Hadjinicolaou, Aristides; El Achkar, Christelle Moufawad; Kamate, Mahesh; Menon, Ramshekhar N.; Jose, Manna; Riordan, Gillian; Kannan, Lakshminarayanan; Jain, Vivek; Manokaran, Ranjith Kumar; Chau, Vann; Donner, Elizabeth J.; Costain, Gregory; Minassian, Berge A.; Jain, Puneet

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Precision medicine for developmental and epileptic encephalopathies in Africa-strategies for a resource-limited setting

GENETICS IN MEDICINE

IF6.2

2023-02-01

OAAI

Esterhuizen, Alina I.; Tiffin, Nicki; Riordan, Gillian; Wessels, Marie; Burman, Richard J.; Aziz, Miriam C.; Calhoun, Jeffrey D.; Gunti, Jonathan; Amiri, Ezra E.; Ramamurthy, Aishwarya; Bamshad, Michael J.; Mefford, Heather C.; Ramesar, Raj; Wilmshurst, Jo M.; Carvill, Gemma L.

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MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load

EBIOMEDICINE

IF10.8

2018-04-01

OAAI

Ng, Yi Shiau; Lax, Nichola Z.; Maddison, Paul; Alston, Charlotte L.; Blakely, Emma L.; Hepplewhite, Philippa D.; Riordan, Gillian; Meldau, Surita; Chinnery, Patrick F.; Pierre, Germaine; Chronopoulou, Efstathia; Du, Ailian; Hughes, Imelda; Morris, Andrew A.; Kamakari, Smaragda; Chrousos, Georgia; Rodenburg, Richard J.; Saris, Christiaan G. J.; Feeney, Catherine; Hardy, Steven A.; Sakakibara, Takafumi; Sudo, Akira; Okazaki, Yasushi; Murayama, Kei; Mundy, Helen; Hanna, Michael G.; Ohtake, Akira; Schaefer, Andrew M.; Champion, Mike P.; Turnbull, Doug M.; Taylor, Robert W.; Pitceathly, Robert D. S.; McFarland, Robert; Gorman, Grainne S.

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Progressive deafness-dystonia due to SERAC1 mutations: A study of 67 cases

ANNALS OF NEUROLOGY

IF7.7

2017-12-20

OAAI

Maas, Roeltje R.; Iwanicka-Pronicka, Katarzyna; Ucar, Sema Kalkan; Alhaddad, Bader; AlSayed, Moeenaldeen; Al-Owain, Mohammed A.; Al-Zaidan, Hamad I.; Balasubramaniam, Shanti; Baric, Ivo; Bubshait, Dalal K.; Burlina, Alberto; Christodoulou, John; Chung, Wendy K.; Colombo, Roberto; Darin, Niklas; Freisinger, Peter; Garcia Silva, Maria Teresa; Grunewald, Stephanie; Haack, Tobias B.; van Hasselt, Peter M.; Hikmat, Omar; Hoerster, Friederike; Isohanni, Pirjo; Ramzan, Khushnooda; Kovacs-Nagy, Reka; Krumina, Zita; Martin-Hernandez, Elena; Mayr, Johannes A.; McClean, Patricia; De Meirleir, Linda; Naess, Karin; Ngu, Lock H.; Pajdowska, Magdalena; Rahman, Shamima; Riordan, Gillian; Riley, Lisa; Roeben, Benjamin; Rutsch, Frank; Santer, Rene; Schiff, Manuel; Seders, Martine; Sequeira, Silvia; Sperl, Wolfgang; Staufner, Christian; Synofzik, Matthis; Taylor, Robert W.; Trubicka, Joanna; Tsiakas, Konstantinos; Unal, Ozlem; Wassmer, Evangeline; Wedatilake, Yehani; Wolff, Toni; Prokisch, Holger; Morava, Eva; Pronicka, Ewa; Wevers, Ron A.; de Brouwer, Arjan P.; Wortmann, Saskia B.

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Understanding the Implications of Mitochondrial DNA Variation in the Health of Black Southern African Populations: The 2014 Workshop

HUMAN MUTATION

IF3.7

2015-04-22

OAAI

van der Westhuizen, Francois H.; Sinxadi, Phumla Z.; Dandara, Collet; Smuts, Izelle; Riordan, Gillian; Meldau, Surita; Malik, Afshan N.; Sweeney, Mary G.; Tsai, Yuchia; Towers, Gordon W.; Louw, Roan; Gorman, Grainne S.; Payne, Brendan A.; Soodyall, Himla; Pepper, Michael S.; Elson, Joanna L.

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Childhood secondary (Symptomatic) epilepsy, seizure control, and intellectual handicap in a nontropical region of South Africa

EPILEPSIA

IF6.6

2005-08-02

OAAI

Leary, PM; Riordan, G; Schlegel, B; Morris, S

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Research Directions