Hanan E. Shamseldin

5.3k total citations
55 papers, 1.5k citations indexed

About

Hanan E. Shamseldin is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Hanan E. Shamseldin has authored 55 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 31 papers in Genetics and 9 papers in Cell Biology. Recurrent topics in Hanan E. Shamseldin's work include Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Hanan E. Shamseldin is often cited by papers focused on Genomics and Rare Diseases (14 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genetics and Neurodevelopmental Disorders (8 papers). Hanan E. Shamseldin collaborates with scholars based in Saudi Arabia, United States and Egypt. Hanan E. Shamseldin's co-authors include Fowzan S. Alkuraya, Mais Hashem, Ranad Shaheen, Tarfa Al‐Sheddi, Eissa Faqeih, Niema Ibrahim, Muneera Alshammari, Mustafa A. Salih, Amal Y. Kentab and Hisham Alkhalidi and has published in prestigious journals such as Brain, Hepatology and Journal of Allergy and Clinical Immunology.

In The Last Decade

Hanan E. Shamseldin

55 papers receiving 1.5k citations

Peers

Countries citing papers authored by Hanan E. Shamseldin

Since Specialization

Citations

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

Fields of papers citing papers by Hanan E. Shamseldin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hanan E. Shamseldin. 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 Hanan E. Shamseldin. The network helps show where Hanan E. Shamseldin may publish in the future.

Co-authorship network of co-authors of Hanan E. Shamseldin

This figure shows the co-authorship network connecting the top 25 collaborators of Hanan E. Shamseldin. A scholar is included among the top collaborators of Hanan E. Shamseldin 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 Hanan E. Shamseldin. Hanan E. Shamseldin 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	Genomic analysis of presumed perinatal stroke in Saudi Arabia reveals a strong monogenic contribution 2024 ·Human Genetics ·Muneera Alshammari, Hanan E. Shamseldin, (unknown), (unknown), (unknown), Firdous Abdulwahab, Fowzan S. Alkuraya	1
2	Further delineation of the phenotypic and metabolomic profile of ALDH1L2‐related neurodevelopmental disorder 2024 ·Clinical Genetics ·Mikyoung You, Hanan E. Shamseldin, (unknown), Blake R. Rushing, (unknown), Amal Jaafar, Mais Hashem, Firdous Abdulwahab, Anas M. Abdel Rahman, Natalia I. Krupenko, Fowzan S. Alkuraya, Sergey A. Krupenko	1
3	PRSS8, encoding prostasin, is mutated in patients with autosomal recessive ichthyosis 2023 ·Human Genetics ·Hanan E. Shamseldin, Nada Derar, Hamad Alzaidan, Naif Alhathal, (unknown), Firdous Abdulwahab, Tariq Al‐Zaid, (unknown), (unknown), Fowzan S. Alkuraya	4
4	A founder DBR1 variant causes a lethal form of congenital ichthyosis 2023 ·Human Genetics ·Hanan E. Shamseldin, (unknown), (unknown), Ruslan Al‐Ali, (unknown), (unknown), (unknown), Zuhair Rahbeeni, Fuad Al Mutairi, (unknown), (unknown), Firdous Abdulwahab, (unknown), Peter Bauer, Aida M. Bertoli‐Avella, Fowzan S. Alkuraya	6
5	The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction 2023 ·Prenatal Diagnosis ·(unknown), Karin J. Blakemore, (unknown), Jena L. Miller, (unknown), Hanan E. Shamseldin, Sateesh Maddirevula, Thomas Hays, Billie R. Lianoglou, (unknown), Linda A. Baker, Teresa N. Sparks, Ronald J. Wapner, Fowzan S. Alkuraya, Mary E. Norton, Angie C. Jelin	5
6	Molecular autopsy by proxy in preconception counseling 2021 ·Clinical Genetics ·Malak Alghamdi, (unknown), (unknown), Nouran Adly, (unknown), Amal Alhashem, Abdulaziz Alshahrani, Hanan E. Shamseldin, Fowzan S. Alkuraya, Majid Alfadhel	6
7	Mitochondrial “dysmorphology” in variant classification 2021 ·Human Genetics ·Hanan E. Shamseldin, Amal Alhashem, Brahim Tabarki, Firdous Abdulwahab, Mais Hashem, Rachid Sougrat, Fowzan S. Alkuraya	3
8	PLXNA2 as a candidate gene in patients with intellectual disability 2021 ·American Journal of Medical Genetics Part A ·(unknown), Hanan E. Shamseldin, Turki H. Albatti, Mais Hashem, Nour Ewida, Firdous Abdulwahab, Fowzan S. Alkuraya	9
9	An exome-first approach to aid in the diagnosis of primary ciliary dyskinesia 2020 ·Human Genetics ·Hanan E. Shamseldin, (unknown), (unknown), (unknown), (unknown), Muslim M. Alsaadi, (unknown), Amal Alhashem, (unknown), (unknown), Niema Ibrahim, Jason Yang, Firdous Abdulwahab, Mais Hashem, Raghu R. Chivukula, Fowzan S. Alkuraya	16
10	Confirming the recessive inheritance of PERP‐related erythrokeratoderma 2020 ·Clinical Genetics ·Nisha Patel, (unknown), Eman Alobeid, Tarfa Alshidi, (unknown), Firdous Abdulwahab, Hanan E. Shamseldin, Fowzan S. Alkuraya	4
11	NUP214 deficiency causes severe encephalopathy and microcephaly in humans 2019 ·Human Genetics ·Hanan E. Shamseldin, Nawal Makhseed, Niema Ibrahim, Tarfa Al‐Sheddi, Eman Alobeid, Firdous Abdulwahab, Fowzan S. Alkuraya	14
12	MDH1 deficiency is a metabolic disorder of the malate–aspartate shuttle associated with early onset severe encephalopathy 2019 ·Human Genetics ·(unknown), Hanan E. Shamseldin, Amal Alhashem, Mais Hashem, Firdous Abdulwahab, (unknown), (unknown), Fried Zwartkruis, (unknown), Sabine A. Fuchs, Nanda M. Verhoeven‐Duif, Judith Jans, Fowzan S. Alkuraya	40
13	WDR45B‐related intellectual disability, spastic quadriplegia, epilepsy, and cerebral hypoplasia: A consistent neurodevelopmental syndrome 2017 ·Clinical Genetics ·Jehan Suleiman, Diane Allingham‐Hawkins, Mais Hashem, Hanan E. Shamseldin, Fowzan S. Alkuraya, Ayman W. El‐Hattab	30
14	Novel copy number variants and major limb reduction malformation: Report of three cases 2016 ·American Journal of Medical Genetics Part A ·Hanan E. Shamseldin, Shams Anazi, Salma M. Wakil, Eissa Faqeih, Heba Y. El Khashab, Mustafa A. Salih, Mohammad M. Al‐Qattan, Mais Hashem, (unknown), Fowzan S. Alkuraya	8
15	A lethal phenotype associated with tissue plasminogen deficiency in humans 2016 ·Human Genetics ·Hanan E. Shamseldin, Abdulrahman Aldeeri, (unknown), Abdulrahman Alsultan, Mais Hashem, Fowzan S. Alkuraya	1
16	ANKS3 is mutated in a family with autosomal recessive laterality defect 2016 ·Human Genetics ·Hanan E. Shamseldin, Toma A. Yakulov, Amal Hashem, Gerd Walz, Fowzan S. Alkuraya	15
17	GOLGA2, encoding a master regulator of golgi apparatus, is mutated in a patient with a neuromuscular disorder 2016 ·Human Genetics ·Hanan E. Shamseldin, (unknown), Majid Alfadhel, Vandana Gupta, Fowzan S. Alkuraya	31
18	Clinical genomics can facilitate countrywide estimation of autosomal recessive disease burden 2016 ·Genetics in Medicine ·Mohamed Abouelhoda, (unknown), Mohamed El-Kalioby, Nisha Patel, Hanan E. Shamseldin, Dorota Monies, Nada Al Tassan, Khushnooda Ramzan, Faiqa Imtiaz, Ranad Shaheen, Fowzan S. Alkuraya	67
19	Increasing the sensitivity of clinical exome sequencing through improved filtration strategy 2016 ·Genetics in Medicine ·Hanan E. Shamseldin, Sateesh Maddirevula, Eissa Faqeih, Niema Ibrahim, Mais Hashem, Ranad Shaheen, Fowzan S. Alkuraya	43
20	Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans 2015 ·Human Genetics ·Hanan E. Shamseldin, Laura L. Smith, Amal Y. Kentab, Hisham Alkhalidi, Brady J. Summers, (unknown), Yong Xiong, Vandana Gupta, Fowzan S. Alkuraya	34

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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