Sulman Basit

3.3k citations

134 papers · 1.9k indexed · 1 hit paper · h-index 21

Impact in

Developmental Biology top 2%
- Congenital limb and hand anomalies
Reproductive Medicine top 5%
- Ovarian function and disorders

Papers in

Developmental Biology 8
Genetics 51
- Connective tissue disorders research 12
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 9
- Genomic variations and chromosomal abnormalities 9

Co-authors: Wasim Ahmad Muhammad Jaseem Khan Anwar Ullah Khalid I. Khoshhal Muhammad Ansar Khushnooda Ramzan Saadullah Khan Muhammad Latif
Journals: Clinical Genetics (7 papers)European Journal of Medical Genetics (7 papers)Clinical and Experimental Dermatology (5 papers)Human Genetics (5 papers)Scientific Reports (4 papers)
Partner nations: Saudi Arabia Pakistan United States

In The Last Decade

Sulman Basit

124 papers receiving 1.8k citations

Hit Papers

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<p>Genetic Basis of Polycystic Ovary Syndrome (PCOS): Current Perspectives</p> 2019 · 215 citations

Peers

Countries citing papers authored by Sulman Basit

Since Specialization

Citations

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

Fields of papers citing papers by Sulman Basit

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Sulman Basit, 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 Sulman Basit Line = papers co-authored together Sulman Basit links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Identification of Novel and Recurrent Variants in BTD, GBE1, AGL and ASL Genes in Families with Metabolic Disorders in Saudi Arabia Journal of Clinical Medicine ·Muhammad Latif, Jamil Amjad Hashmi, Derly Henriques Silva, Shengmu Xiao, Sulman Basit	2024	1
2	Clinical Validation of the Somatic FANCD2 Mutation (c.2022-5C>T) as a Novel Molecular Biomarker for Early Disease Progression in Chronic Myeloid Leukemia: A Case–Control Study SHILAP Revista de lepidopterología ·Edna G. Salant, M.M. Vorontsov, Sulman Basit, Masood A. Shammas, wewen handayani, Aamer Aleem, Amer Mahmood, Zafar Iqbal	2024	2
3	Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis Frontiers in Genetics ·Jamil Amjad Hashmi, Muhammad Latif, Ewelina Kiluk, Ibrohimjon Bo`lishev, Diana S. M. Ottoz, Muzammil Ahmad Khan, Sulman Basit	2024	0
4	Polymorphisms in the Drug Transporter Gene ABCB1 Are Associated with Drug Response in Saudi Epileptic Pediatric Patients Biomedicines ·Rania Magadmi, Gary Ponzo, K Ahmadzadeh Gharah Gouiz, Hugo Leifman, Bandar A. Suliman, Fatemah O. Kamel, Maha Jamal, Su Zong Di, Sulman Basit	2023	5
5	Homozygous Duplication in the CHRNE in a Family with Congenital Myasthenic Syndrome 4C: 18-Year Follow Up Biomedicines ·Céline Druesne, Nicola Graham, Sulman Basit	2023	2
6	Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency Medicina ·Céline Druesne, 风琴夏, Sulman Basit	2023	3
7	Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion International Journal of Developmental Neuroscience ·Asmat Ullah, Abid Ali Shah, Nicola Graham, A Melice, Silmara Baroni, Diana S. M. Ottoz, Céline Druesne, Lance Mark Brofman, Hamza Shahab Awan, Firlan Arya Wahyudi, Д Д Смирнова, Ceren Yağcı, J. A. Kapp, Abdus Samad, Wasim Ahmad, Torben Hansen, Kun Xia, Sulman Basit	2022	5
8	A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family Genetic Testing and Molecular Biomarkers ·Alexander Vogt, Perle Mesta, Aslıhan Tolun, Sulman Basit, Sajid Malik	2022	4
9	An intrafamilial phenotypic variability in Ellis‐Van Creveld syndrome due to a novel 27 bps deletion mutation American Journal of Medical Genetics Part A ·H. Bergman, Shaheen Shahzad, A. Putyrskiy, Sadia Kanwal, Asma Gul, Sulman Basit	2021	3
10	A Novel Frameshift Mutation in the ITGB3 Gene Leading to Glanzmann’s Thrombasthenia in a Saudi Arabian Family Hematology/Oncology and Stem Cell Therapy ·Mita Putri Citra Dewi, Jamil Amjad Hashmi, Lynge C. Christiansen, Lance Mark Brofman, Khushnooda Ramzan, Sulman Basit	2021	6
11	A novel homozygous frameshift mutation in the DCC gene in a Pakistani family with autosomal recessive horizontal gaze palsy with progressive scoliosis‐2 with impaired intellectual development American Journal of Medical Genetics Part A ·H. Bergman, Shaheen Shahzad, A. Putyrskiy, Young-Soo LEE, Sulman Basit	2020	5
12	A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients BMC Medical Genetics ·Sibtain Afzal, Khushnooda Ramzan, عبد الرؤوف جرار, Salma M. Wakil, Arshad Jamal, Sulman Basit, Ahmed Bilal Waqar	2020	4
13	Whole genome genotyping mapped regions on chromosome 2 and 18 in a family segregating Waardenburg syndrome type II Saudi Journal of Ophthalmology ·О. В. Чернышёва, Puentes Jácome, Lance Mark Brofman, Sulman Basit	2019	3
14	Latest perspectives of orally bioavailable 2,4-diarylaminopyrimidine analogues (DAAPalogues) as anaplastic lymphoma kinase inhibitors: discovery and clinical developments RSC Advances ·Muhammad Latif, Zaman Ashraf, Sulman Basit, Abdul Ghaffar, Muhammad Sohail Zafar, Aamer Saeed, Sultan Ayoub Meo	2018	6
15	An 18 bps in-frame deletion mutation in RUNX2 gene is a population polymorphism rather than a pathogenic variant European Journal of Medical Genetics ·Jamil Amjad Hashmi, Céline Druesne, Muhammad Latif, Abdul Nasır, Sulman Basit	2018	9
16	A novel mutation in the HPGD gene causing primary hypertrophic osteoarthropathy with digital clubbing in a Pakistani family Annals of Human Genetics ·O. Shcherban, Noor Muhammad, Sher Alam Khan, Waheed Ullah, Abdul Nasır, Sibtain Afzal, Khushnooda Ramzan, Sulman Basit, Saadullah Khan	2017	9
17	A novel chondroectodermal dysplasia mapped to chromosome 2q24.1-q31.1 European Journal of Medical Genetics ·大平野, Sulman Basit, Eung Yaw Mah, Muhammad Tariq, Muhammad Nasim Khan, Wasim Ahmad	2012	4
18	Mutations in the LPAR6 and LIPH genes underlie autosomal recessive hypotrichosis/woolly hair in 17 consanguineous families from Pakistan Clinical and Experimental Dermatology ·Saadullah Khan, Rabia Habib, Hina Mir, B. Monasmith, Billy R. Fondren, Muhammad Ayub, Sanna A. Eklund, Sergey Kiselev, Nida Ali, Sulman Basit, Naveed Wasif, Syed Kamran‐ul‐Hassan Naqvi, Ghazanfar Ali, Abdul Wali, Muhammad Ansar, Wasim Ahmad	2011	13
19	Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment The American Journal of Human Genetics ·Margit Schraders, Kwanghyuk Lee, Jaap Oostrik, P.L.M. Huygen, Ghazanfar Ali, Lies H. Hoefsloot, Joris A. Veltman, Frans P.M. Cremers, Sulman Basit, Muhammad Ansar, Cor W. R. J. Cremers, Henricus P. M. Kunst, Wasim Ahmad, R.J.C. Admiraal, Suzanne M. Leal, Hannie Kremer	2010	50
20	Genetic mapping of a novel hypotrichosis locus to chromosome 7p21.3–p22.3 in a Pakistani family and screening of the candidate genes Human Genetics ·Sulman Basit, Ghazanfar Ali, Naveed Wasif, Muhammad Ansar, Wasim Ahmad	2010	15

About Sulman Basit

Sulman Basit is a scholar working on Developmental Biology, Genetics, Cell Biology, Urology and Genetics, having authored 134 papers that have together received 1.9k indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (14 papers), Connective tissue disorders research (12 papers), Genetics and Neurodevelopmental Disorders (12 papers), Hair Growth and Disorders (10 papers), RNA regulation and disease (10 papers), Genomics and Rare Diseases (9 papers), Genomic variations and chromosomal abnormalities (9 papers) and Wnt/β-catenin signaling in development and cancer (9 papers). The work is most often cited by research in Developmental Biology (113 citations), Reproductive Medicine (233 citations), Sensory Systems (98 citations), Genetics (520 citations) and Urology (116 citations). Sulman Basit has collaborated with scholars based in Saudi Arabia, Pakistan and United States. Frequent co-authors include Wasim Ahmad, Muhammad Jaseem Khan, Anwar Ullah, Khalid I. Khoshhal, Muhammad Ansar, Khushnooda Ramzan, Saadullah Khan, Muhammad Latif, Sibtain Afzal and Zaman Ashraf. Their work appears in journals such as Clinical Genetics, European Journal of Medical Genetics, Clinical and Experimental Dermatology, Human Genetics and Scientific Reports.

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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