Salma Ben‐Salem

1.1k citations

26 papers · 470 indexed · h-index 13

Co-authors: Bassam R. Ali Lihadh Al‐Gazali Aisha Al‐Shamsi Varadha Balaji Venkadakrishnan Anne John Jozef Hertecant Hammadi Ayadi Peter Söderkvist
Topics: Ubiquitin and proteasome pathways (5 papers)Genomics and Rare Diseases (3 papers)Hedgehog Signaling Pathway Studies (3 papers)
Cited by: Genetics Ophthalmology Clinical Biochemistry
Journals: Nature Genetics The Journal of Immunology Gene
Partner nations: United Arab Emirates United States Tunisia

In The Last Decade

Salma Ben‐Salem

26 papers receiving 465 citations

Peers

Countries citing papers authored by Salma Ben‐Salem

Since Specialization

Citations

This map shows the geographic impact of Salma Ben‐Salem'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 Salma Ben‐Salem with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Salma Ben‐Salem more than expected).

Fields of papers citing papers by Salma Ben‐Salem

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Salma Ben‐Salem. 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 Salma Ben‐Salem. The network helps show where Salma Ben‐Salem may publish in the future.

Co-authorship network of co-authors of Salma Ben‐Salem

This figure shows the co-authorship network connecting the top 25 collaborators of Salma Ben‐Salem. A scholar is included among the top collaborators of Salma Ben‐Salem 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 Salma Ben‐Salem. Salma Ben‐Salem is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Targeting NANOG and FAK via Cx26-derived Cell-penetrating Peptides in Triple-negative Breast Cancer 2023 ·Molecular Cancer Therapeutics ·Erin E. Mulkearns-Hubert,(unknown),Salma Ben‐Salem,Rashmi Bharti,(unknown),Sadie Johnson,(unknown),(unknown),Smarajit Bandyopadhyay,Charis Eng,(unknown),Justin D. Lathia,Ofer Reizes	6
2	Diversity in Androgen Receptor Action Among Treatment-naïve Prostate Cancers Is Reflected in Treatment Response Predictions and Molecular Subtypes 2020 ·European Urology Open Science ·Salma Ben‐Salem,Qiang Hu,Yang Liu,Mohammed Alshalalfa,(unknown),Irène Wang,Varadha Balaji Venkadakrishnan,Dhirodatta Senapati,Sangeeta Kumari,Deli Liu,Andrea Sboner,Christopher E. Barbieri,Felix Y. Feng,Jean-Noël Billaud,Elai Davicioni,Song Liu,Hannelore V. Heemers	5
3	AR-dependent phosphorylation and phospho-proteome targets in prostate cancer 2020 ·Endocrine Related Cancer ·Varadha Balaji Venkadakrishnan,Salma Ben‐Salem,Hannelore V. Heemers	9
4	Compound heterozygous variants in the multiple PDZ domain protein (MPDZ) cause a case of mild non-progressive communicating hydrocephalus 2018 ·BMC Medical Genetics ·(unknown),Aisha Al‐Shamsi,Jehan Suleiman,Salma Ben‐Salem,Anne John,Ranjit Vijayan,Bassam R. Ali,Lihadh Al‐Gazali	10
5	Defect in phosphoinositide signalling through a homozygous variant in PLCB3 causes a new form of spondylometaphyseal dysplasia with corneal dystrophy 2017 ·Journal of Medical Genetics ·Salma Ben‐Salem,(unknown),Nara L. M. Sobreira,Angeline M. Lyon,Aisha Al‐Shamsi,Barira Islam,Nadia Akawi,Anne John,(unknown),(unknown),David Valle,Bassam R. Ali,Lihadh Al‐Gazali	7
6	A homozygous splicing mutation in ELAC2 suggests phenotypic variability including intellectual disability with minimal cardiac involvement 2016 ·Orphanet Journal of Rare Diseases ·Nadia Akawi,Salma Ben‐Salem,Jozef Hertecant,Anne John,(unknown),(unknown),Bassam R. Ali,Lihadh Al‐Gazali	12
7	A Novel Single-Nucleotide Deletion (c.1020delA) in NSUN2 Causes Intellectual Disability in an Emirati Child 2015 ·Journal of Molecular Neuroscience ·(unknown),Aisha Al‐Shamsi,Salma Ben‐Salem,Bassam R. Ali,Lihadh Al‐Gazali	42
8	Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings 2015 ·American Journal of Medical Genetics Part A ·Salma Ben‐Salem,Nara Sobreira,Nadia Akawi,Aisha Al‐Shamsi,Anne John,(unknown),David Valle,Bassam R. Ali,Lihadh Al‐Gazali	11
9	Mutation spectrum of Joubert syndrome and related disorders among Arabs 2014 ·Human Genome Variation ·Salma Ben‐Salem,Aisha Al‐Shamsi,Joseph G. Gleeson,Bassam R. Ali,Lihadh Al‐Gazali	30
10	The mutational spectrum of the NF1 gene in neurofibromatosis type I patients from UAE 2014 ·Child s Nervous System ·Salma Ben‐Salem,Aisha Al‐Shamsi,Bassam R. Ali,Lihadh Al‐Gazali	7
11	Asparagine synthetase deficiency detected by whole exome sequencing causes congenital microcephaly, epileptic encephalopathy and psychomotor delay 2014 ·Metabolic Brain Disease ·Salma Ben‐Salem,Joseph G. Gleeson,Aisha Al‐Shamsi,Barira Islam,Jozef Hertecant,Bassam R. Ali,Lihadh Al‐Gazali	35
12	A Novel Whole Exon Deletion in WWOX Gene Causes Early Epilepsy, Intellectual Disability and Optic Atrophy 2014 ·Journal of Molecular Neuroscience ·Salma Ben‐Salem,Aisha Al‐Shamsi,Anne John,Bassam R. Ali,Lihadh Al‐Gazali	36
13	Transaldolase deficiency caused by the homozygous p.R192C mutation of the TALDO1 gene in four Emirati patients with considerable phenotypic variability 2014 ·European Journal of Pediatrics ·Aisha Al‐Shamsi,Salma Ben‐Salem,Jozef Hertecant,Fatma Al‐Jasmi	15
14	Posterior microphthalmia and nanophthalmia in Tunisia caused by a founder c.1059_1066insC mutation of the PRSS56 gene 2013 ·Gene ·Mariem Ben Saïd,(unknown),Salma Ben‐Salem,(unknown),(unknown),W. Bouassida,Z. Benzina,Hammadi Ayadi,Peter Söderkvist,L. El Matri,Mounira Hmani‐Aifa	17
15	Analysis of two Arab families reveals additional support for a DFNB2 nonsyndromic phenotype of MYO7A 2013 ·Molecular Biology Reports ·Salma Ben‐Salem,Heidi L. Rehm,Patrick J. Willems,(unknown),Hammadi Ayadi,Bassam R. Ali,Lihadh Al‐Gazali	7
16	Determination of the CCR5∆32 frequency in Emiratis and Tunisians and the screening of the CCR5 gene for novel alleles in Emiratis 2013 ·Gene ·(unknown),Salma Ben‐Salem,(unknown),Fatma Ayadi,Lihadh Al‐Gazali,Bassam R. Ali	7
17	A Novel Aberrant Splice Site Mutation in <b><i>RAB23</i></b> Leads to an Eight Nucleotide Deletion in the mRNA and Is Responsible for Carpenter Syndrome in a Consanguineous Emirati Family 2012 ·Molecular Syndromology ·Salma Ben‐Salem,(unknown),Bassam R. Ali,Lihadh Al‐Gazali	18
18	Clinical and molecular analysis of isovaleric acidemia patients in the United Arab Emirates reveals remarkable phenotypes and four novel mutations in the IVD gene 2012 ·European Journal of Medical Genetics ·Jozef Hertecant,(unknown),(unknown),(unknown),(unknown),Salma Ben‐Salem,Fatma Al‐Jasmi,Lihadh Al‐Gazali,Said Al‐Yahyaee,Bassam R. Ali	13
19	Alteration of the serine protease PRSS56 causes angle-closure glaucoma in mice and posterior microphthalmia in humans and mice 2011 ·Nature Genetics ·K. Saidas Nair,Mounira Hmani‐Aifa,(unknown),(unknown),Salma Ben‐Salem,Danilo G. Macalinao,Ioan M Cosma,W. Bouassida,(unknown),Z. Benzina,Ileana Soto,Peter Söderkvist,Gareth R. Howell,Richard S. Smith,Hammadi Ayadi,Simon W. M. John	78
20	A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1 2009 ·Human Genetics ·Mounira Hmani‐Aifa,Salma Ben‐Salem,Z. Benzina,W. Bouassida,R. Messaoud,(unknown),Moncef Khairallah,Ahmed Rebaï,(unknown),Peter Söderkvist,Hammadi Ayadi	15

About Salma Ben‐Salem

Salma Ben‐Salem is a scholar working on Genetics, Clinical Biochemistry and Molecular Biology, having authored 26 papers that have together received 470 indexed citations. Recurring topics across this work include Ubiquitin and proteasome pathways (5 papers), Genomics and Rare Diseases (3 papers) and Hedgehog Signaling Pathway Studies (3 papers). The work is most often cited by research in Genetics (209 citations), Ophthalmology (64 citations) and Clinical Biochemistry (37 citations). Salma Ben‐Salem has collaborated with scholars based in United Arab Emirates, United States and Tunisia. Frequent co-authors include Bassam R. Ali, Lihadh Al‐Gazali, Aisha Al‐Shamsi, Varadha Balaji Venkadakrishnan, Anne John, Jozef Hertecant, Hammadi Ayadi, Peter Söderkvist, W. Bouassida and Mounira Hmani‐Aifa. Their work appears in journals such as Nature Genetics, The Journal of Immunology and Gene.

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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