Salah A. Elmalik

677 citations

12 papers · 232 indexed · h-index 9

Co-authors: Mustafa A. Salih Abdulmajeed AlDrees Mohammad M. Kabiraj Ibrahim A. Alorainy Arif O. Khan Darren T. Oystreck M. Kœnig Clotilde Lagier‐Tourenne
Topics: Neurological diseases and metabolism (5 papers)Porphyrin Metabolism and Disorders (3 papers)Metabolism and Genetic Disorders (3 papers)
Cited by: Neurology Clinical Biochemistry Cellular and Molecular Neuroscience
Journals: PLoS ONE Brain Ophthalmology
Partner nations: Saudi Arabia France Germany

In The Last Decade

Salah A. Elmalik

12 papers receiving 227 citations

Peers

Countries citing papers authored by Salah A. Elmalik

Since Specialization

Citations

This map shows the geographic impact of Salah A. Elmalik's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Salah A. Elmalik with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Salah A. Elmalik more than expected).

Fields of papers citing papers by Salah A. Elmalik

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Salah A. Elmalik. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Salah A. Elmalik. The network helps show where Salah A. Elmalik may publish in the future.

Co-authorship network of co-authors of Salah A. Elmalik

This figure shows the co-authorship network connecting the top 25 collaborators of Salah A. Elmalik. A scholar is included among the top collaborators of Salah A. Elmalik based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Salah A. Elmalik. Salah A. Elmalik is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15) 2020 ·BMC Neurology ·Mohammed Zain Seidahmed,Muddathir H. Hamad,Albandary AlBakheet,Salah A. Elmalik,Abdulmajeed AlDrees,(unknown),Ibrahim A. Alorainy,(unknown),Dilek Çolak,Mustafa A. Salih,Namik Kaya	11
2	Descriptive Patterns of Deafness Among Pre-School Saudi Children Aged Two to Five Years Visiting Neurology Clinic From 2012 to 2017 2020 ·Cureus ·Salah A. Elmalik,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown)	1
3	Intra-familial phenotypic heterogeneity in a Sudanese family with DARS2-related leukoencephalopathy, brainstem and spinal cord involvement and lactate elevation: a case report 2018 ·BMC Neurology ·(unknown),Liena E. O. Elsayed,(unknown),Mustafa A. Salih,Sarah El-Sadig,Mutaz Amin,Mahmoud Koko,(unknown),(unknown),(unknown),Salah A. Elmalik,Alexis Brice,Ammar Ahmed,Giovanni Stévanin	11
4	Ophthalmic features ofPLA2G6-related paediatric neurodegeneration with brain iron accumulation 2014 ·British Journal of Ophthalmology ·(unknown),Abdulmajeed AlDrees,Salah A. Elmalik,Hamdy H. Hassan,M. Kœnig,Giovanni Stévanin,Hamid Azzedine,Mustafa A. Salih	9
5	New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations 2013 ·PLoS ONE ·Mustafa A. Salih,Emeline Mundwiller,Arif O. Khan,Abdulmajeed AlDrees,Salah A. Elmalik,Hamdy H. Hassan,Mohammed Al‐Owain,Hisham Alkhalidi,István Katona,Mohammad M. Kabiraj,Roman Chrast,Amal Y. Kentab,Hamad Alzaidan,Richard J. Rodenburg,Thomas M. Bosley,Joachim Weis,M. Kœnig,Giovanni Stévanin,Hamid Azzedine	38
6	C19orf12 mutation leads to a pallido-pyramidal syndrome 2013 ·Gene ·Michael C. Kruer,Mustafa A. Salih,Catherine Mooney,(unknown),Salah A. Elmalik,Mohammad M. Kabiraj,Arif O. Khan,Reema Paudel,Henry Houlden,Hamid Azzedine,Fowzan S. Alkuraya	22
7	Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations 2013 ·PLoS ONE ·Mustafa A. Salih,Emeline Mundwiller,Arif O. Khan,Abdulmajeed AlDrees,Salah A. Elmalik,Hamdy H. Hassan,Mohammed Al‐Owain,Hisham Alkhalidi,István Katona,Mohammad M. Kabiraj,Roman Chrast,Amal Y. Kentab,Hamad Alzaidan,Richard J. Rodenburg,Thomas M. Bosley,Joachim Weis,Michel Kœnig,Giovanni Stévanin,Hamid Azzedine	6
8	A newly recognized autosomal recessive syndrome affecting neurologic function and vision 2013 ·American Journal of Medical Genetics Part A ·Mustafa A. Salih,Andreas Tzschach,Darren T. Oystreck,Hamdy H. Hassan,Abdulmajeed AlDrees,Salah A. Elmalik,Heba Y. El Khashab,Thomas F. Wienker,Khaled K. Abu‐Amero,Thomas M. Bosley	7
9	The neurology of carbonic anhydrase type II deficiency syndrome 2011 ·Brain ·Thomas M. Bosley,Mustafa A. Salih,Ibrahim A. Alorainy,Mohammad Zahirul Islam,Darren T. Oystreck,(unknown),(unknown),(unknown),(unknown),Sigri Beckers,Liesbeth Van Wesenbeeck,Bram Perdu,Abdulmajeed AlDrees,Salah A. Elmalik,Wim Van Hul,Khaled K. Abu‐Amero	27
10	Rundataxin, a novel protein with RUN and diacylglycerol binding domains, is mutant in a new recessive ataxia 2010 ·Brain ·Mirna Assoum,Mustafa A. Salih,Nathalie Drouot,Dorra H’mida-Ben Brahim,Clotilde Lagier‐Tourenne,Abdulmajeed AlDrees,Salah A. Elmalik,(unknown),(unknown),Mohammad M. Kabiraj,M. Kœnig	33
11	Ophthalmic Features of Joubert Syndrome 2008 ·Ophthalmology ·Arif O. Khan,Darren T. Oystreck,(unknown),Abdulmajeed AlDrees,Salah A. Elmalik,Ibrahim A. Alorainy,Mustafa A. Salih	34
12	A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23 2007 ·Brain ·Moez Gribaa,Mustafa A. Salih,Mathieu Anheim,Clotilde Lagier‐Tourenne,(unknown),Nathalie Drouot,(unknown),Salah A. Elmalik,Mohammad M. Kabiraj,(unknown),(unknown),Christine Bétard,Hans H. Goebel,Michel Kœnig	33

About Salah A. Elmalik

Salah A. Elmalik is a scholar working on Neurology, Clinical Biochemistry and Sensory Systems, having authored 12 papers that have together received 232 indexed citations. Recurring topics across this work include Neurological diseases and metabolism (5 papers), Porphyrin Metabolism and Disorders (3 papers) and Metabolism and Genetic Disorders (3 papers). The work is most often cited by research in Neurology (78 citations), Clinical Biochemistry (35 citations) and Cellular and Molecular Neuroscience (63 citations). Salah A. Elmalik has collaborated with scholars based in Saudi Arabia, France and Germany. Frequent co-authors include Mustafa A. Salih, Abdulmajeed AlDrees, Mohammad M. Kabiraj, Ibrahim A. Alorainy, Arif O. Khan, Darren T. Oystreck, M. Kœnig, Clotilde Lagier‐Tourenne, Hamid Azzedine and Thomas M. Bosley. Their work appears in journals such as PLoS ONE, Brain and Ophthalmology.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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