S. Bahl

648 total citations
4 papers, 217 citations indexed

About

S. Bahl is a scholar working on Molecular Biology, Nephrology and Genetics. According to data from OpenAlex, S. Bahl has authored 4 papers receiving a total of 217 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 1 paper in Nephrology and 1 paper in Genetics. Recurrent topics in S. Bahl's work include Glycosylation and Glycoproteins Research (1 paper), Genetic Syndromes and Imprinting (1 paper) and DNA Repair Mechanisms (1 paper). S. Bahl is often cited by papers focused on Glycosylation and Glycoproteins Research (1 paper), Genetic Syndromes and Imprinting (1 paper) and DNA Repair Mechanisms (1 paper). S. Bahl collaborates with scholars based in India, United States and Israel. S. Bahl's co-authors include Stacey Gabriel, Eric S. Lander, Jennifer R. Brown, Reina Improgo, Grace Tiao, Jaegil Kim, Siddha Kasar, Nicholas J. Haradhvala, H. T. Kim and Stacey M. Fernandes and has published in prestigious journals such as Nature Communications, Human Molecular Genetics and Annals of Human Genetics.

In The Last Decade

S. Bahl

4 papers receiving 216 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
S. Bahl India	3	125	64	51	51	47	4	217
Alan Stuart Canada	7	95 0.8×	59 0.9×	46 0.9×	36 0.7×	30 0.6×	16	224
Simona Wagner Canada	9	192 1.5×	63 1.0×	16 0.3×	16 0.3×	22 0.5×	10	352
Ken-ichi Sawada Japan	9	214 1.7×	138 2.2×	81 1.6×	55 1.1×	28 0.6×	9	396
Chantelle Hudson United Kingdom	8	221 1.8×	91 1.4×	40 0.8×	36 0.7×	15 0.3×	10	305
Danielle Gattis United States	9	247 2.0×	59 0.9×	58 1.1×	8 0.2×	127 2.7×	9	383
Diana Dunshee United States	6	152 1.2×	34 0.5×	14 0.3×	23 0.5×	26 0.6×	11	236
Danika Di Giacomo Italy	9	189 1.5×	29 0.5×	25 0.5×	20 0.4×	11 0.2×	17	292
Marc B. Kaye United States	4	272 2.2×	37 0.6×	34 0.7×	28 0.5×	24 0.5×	7	357
Louise A. Stephen United Kingdom	10	229 1.8×	60 0.9×	22 0.4×	17 0.3×	14 0.3×	23	349
S. Naylor	4	148 1.2×	55 0.9×	21 0.4×	44 0.9×	19 0.4×	5	249

Countries citing papers authored by S. Bahl

Since Specialization

Citations

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

Fields of papers citing papers by S. Bahl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Bahl

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

All Works

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4 of 4 papers shown

1.

Bahl, S.. (2023). Study of Clinical Profile of HCM Patients Carrying 25 BP Deletion in Intron 32 of Cardiac Myosin Binding Protein C (MYBPC3) Gene. International Journal of Science and Research (IJSR). 12(5). 688–695. 1 indexed citations

2.

Kasar, Siddha, Jaegil Kim, Reina Improgo, et al.. (2015). Whole-genome sequencing reveals activation-induced cytidine deaminase signatures during indolent chronic lymphocytic leukaemia evolution. Nature Communications. 6(1). 8866–8866. 138 indexed citations

3.

Bowl, Michael R., Samantha Mirczuk, I. V. Grigorieva, et al.. (2010). Identification and characterization of novel parathyroid-specific transcription factor Glial Cells Missing Homolog B (GCMB) mutations in eight families with autosomal recessive hypoparathyroidism. Human Molecular Genetics. 19(10). 2028–2038. 26 indexed citations

4.

Bahl, S., Uma Mittal, M.P. Sachdeva, et al.. (2005). Evidence of a Common Founder for SCA12 in the Indian Population. Annals of Human Genetics. 69(5). 528–534. 52 indexed citations

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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