Tipu Sultan

1.9k citations
75 papers · 1.2k · h-index 16

Impact in

Papers in

Co-authors
Joseph J Gleeson (6 shared papers)Damir Musaev (4 shared papers)Maha Saad Zaki (4 shared papers)André Reis (3 shared papers)Rasim Özgür Rosti (3 shared papers)Rami Abou Jamra (3 shared papers)Kiely N. James (3 shared papers)Martin W. Breuss (3 shared papers)
Journals
The American Journal of Human Genetics (11 papers)Genetics in Medicine (9 papers)Brain (9 papers)Movement Disorders (3 papers)Brain Communications (2 papers)
Partner nations
United KingdomUnited StatesGermany

In The Last Decade

Tipu Sultan

60 papers receiving 1.2k citations

Peers

Tipu Sultan
Comparison fields: 5 of 62
  • Cellular and Molecular Neuroscience 112
  • Neurology 47
  • Genetics 189
  • Clinical Biochemistry 25
  • Psychiatry and Mental health 100
Replace Lauren Brady with:
Lauren Brady Canada
Eleonora Di Gregorio Italy
Jean-Baptiste Le Pichon United States
Sharyn A. Lincoln United States
Rebecca H. Signer United States
Kristin W. Baranano United States
Agnès Rastetter France
Ginevra Zanni Italy
Lysanne Patry Canada
Keiko Yamamoto Shimojima Japan
Tipu Sultan relative to Lauren Brady Canada Lauren Brady's profile →
Citations per field
00.5×1.5×2×2.4×
Lauren Brady · 1×
Citations per year

Countries citing papers authored by Tipu Sultan

Since Specialization
Citations

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

Fields of papers citing papers by Tipu Sultan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Tipu Sultan. 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 Tipu Sultan. The network helps show where Tipu Sultan may publish in the future.

Co-authors

The 25 scholars most cited alongside Tipu Sultan, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Tipu Sultan Line = papers co-authored together Tipu Sultan links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 75 papers — load more, or switch the sort, to bring in the rest.

#Work
1
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders
Nature Communications ·Vincenzo Salpietro, Christine L. Dixon, Hui Guo, Oscar Daniel Bello, Jana Vandrovcová, Stéphanie Efthymiou, Reza Maroofian, Gali Heimer
2019198
2
Expanding the genetic heterogeneity of intellectual disability
Human Genetics ·Shams Anazi, Sateesh Maddirevula, Vincenzo Salpietro, Yasmine T. Asi, Saud Alsahli, Amal Mohammed Alhashem, Hanan E. Shamseldin, Fatema Alzahrani
2017127
3
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment
The American Journal of Human Genetics ·Vincenzo Salpietro, Nancy T. Malintan, Isabel Llano‐Rivas, Christine G. Spaeth, Stéphanie Efthymiou, Pasquale Striano, Jana Vandrovcová, Maria Concetta Cutrupi
201993
4
Mutations in MBOAT7 , Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features
The American Journal of Human Genetics ·Anide Johansen, Rasim Özgür Rosti, Damir Musaev, Evan Sticca, Ricardo Harripaul, Maha Saad Zaki, Ahmet Okay Çağlayan, Matloob Azam
201674
5
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification
The American Journal of Human Genetics ·Lucía Schottlaender, Rosella Abeti, Zane Jaunmuktane, Carol Macmillan, Viorica Chelban, Benjamin J. O’Callaghan, John McKinley, Reza Maroofian
202069
6
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly
The American Journal of Human Genetics ·Martin W. Breuss, Tipu Sultan, Kiely N. James, Rasim Özgür Rosti, Eric Scott, Damir Musaev, Bansri Furia, André Reis
201651
7
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination
Brain ·Stéphanie Efthymiou, Vincenzo Salpietro, Nancy T. Malintan, Yamna Kriouile, Sara Fortuna, Rita De Zorzi, Katelyn K. Payne, Lindsay B. Henderson
201950
8
Loss of the neural-specific BAF subunit ACTL6B relieves repression of early response genes and causes recessive autism
Proceedings of the National Academy of Sciences ·Wendy Wenderski, Lu Wang, A. Krokhotin, Jessica J. Walsh, Hongjie Li, Hirotaka Shoji, Shereen Georges Ghosh, Renee D. George
202042
9
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants
Brain ·Caroline Neuray, Reza Maroofian, Marcello Scala, Tipu Sultan, Gurpur Shashidhar Pai, Majid Mojarrad, Heba Y. El Khashab, Leigh deHoll
202040
10
PYCR2Mutations cause a lethal syndrome of microcephaly and failure to thrive
Annals of Neurology ·Maha Saad Zaki, Gifty Bhat, Tipu Sultan, Mahmoud Y. Issa, Hea‐Jin Jung, Esra Dikoglu, Laila Selim, Mohamed S. Abdel‐Hamid
201637
11
Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies
Genetics in Medicine ·Gabriel C. Dworschak, Jaya Punetha, Jeshurun C. Kalanithy, Enrico Mingardo, Haktan Bağış Erdem, Zeynep Coban‐Akdemir, Ender Karaca, Tadahiro Mitani
202133
12
Biallelic variants in HPDL, encoding 4-hydroxyphenylpyruvate dioxygenase-like protein, lead to an infantile neurodegenerative condition
Genetics in Medicine ·Shereen Georges Ghosh, Rudy Fabunan, Guoliang Chai, Maha Saad Zaki, Ghada M. H. Abdel‐Salam, Tipu Sultan, Tawfeg Ben‐Omran, Javeria Raza Alvi
202026
13
Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental Syndrome
The American Journal of Human Genetics ·Martin W. Breuss, An Nguyen, Thai B. Nguyen, Valentina Stanley, Kiely N. James, Damir Musaev, Guoliang Chai, Sara A. Wirth
201825
14
Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish
Genetics in Medicine ·Barbara Vona, Patrícia Gonçalves Barbalho, Rauan B. Kaiyrzhanov, Reza Maroofian, Cassidy Petree, Mariasavina Severino, Valentina Stanley, Pratishtha Varshney
202122
15
Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival
Genetics in Medicine ·Michael E. Coulter, Damir Musaev, Ellen M. DeGennaro, Xiaochang Zhang, Katrin Henke, Kiely N. James, Richard S. Smith, R. Sean Hill
202021
16
Homozygous SCN1B variants causing early infantile epileptic encephalopathy 52 affect voltage‐gated sodium channel function
Epilepsia ·Marcello Scala, Stéphanie Efthymiou, Tipu Sultan, Jolien De Waele, Marta Panciroli, Vincenzo Salpietro, Reza Maroofian, Pasquale Striano
202117
17
Autosomal-Recessive Mutations in the tRNA Splicing Endonuclease Subunit TSEN15 Cause Pontocerebellar Hypoplasia and Progressive Microcephaly
The American Journal of Human Genetics ·Martin W. Breuss, Tipu Sultan, Kiely N. James, Rasim Özgür Rosti, Eric Scott, Damir Musaev, Bansri Furia, André Reis
201616
18
Expanding the phenotype of PIGS‐associated early onset epileptic developmental encephalopathy
Epilepsia ·Stéphanie Efthymiou, Marina Dutra‐Clarke, Reza Maroofian, Rauan B. Kaiyrzhanov, Marcello Scala, Javeria Raza Alvi, Tipu Sultan, Marilena Christoforou
202116
19
Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies
Genetics in Medicine ·Reza Maroofian, Büşranur Çavdarlı, Florence Riccardi, Siddharth Banka, Dalal Bubshait, Yun Li, Jozef Hertecant, Shahid Mahmood Baig
202116
20
ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies
The American Journal of Human Genetics ·Gabrielle Lemire, Yoko Itō, Aren E. Marshall, Nicolas Chrestian, Valentina Stanley, Lauren Brady, Mark Andrew Tarnopolsky, Cynthia J. Curry
202115

About Tipu Sultan

Tipu Sultan is a scholar working on Genetics, Psychiatry and Mental health, Clinical Biochemistry, Cellular and Molecular Neuroscience and Neurology, having authored 75 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (16 papers), Epilepsy research and treatment (9 papers), Metabolism and Genetic Disorders (5 papers), Lysosomal Storage Disorders Research (5 papers), Acute Ischemic Stroke Management (3 papers), Hereditary Neurological Disorders (3 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Autoimmune Neurological Disorders and Treatments (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (112 citations), Neurology (47 citations), Genetics (189 citations), Clinical Biochemistry (25 citations) and Psychiatry and Mental health (100 citations). Tipu Sultan has collaborated with scholars based in United Kingdom, United States and Germany. Frequent co-authors include Joseph J Gleeson, Damir Musaev, Maha Saad Zaki, André Reis, Rasim Özgür Rosti, Rami Abou Jamra, Kiely N. James, Martin W. Breuss, Henry Houlden and Fowzan Sami Alkuraya. Their work appears in journals such as The American Journal of Human Genetics, Genetics in Medicine, Brain, Movement Disorders and Brain Communications.

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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