Samarth Bhatt

2.6k total citations
34 papers, 1.0k citations indexed

About

Samarth Bhatt is a scholar working on Genetics, Plant Science and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Samarth Bhatt has authored 34 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 15 papers in Plant Science and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Samarth Bhatt's work include Genomic variations and chromosomal abnormalities (18 papers), Chromosomal and Genetic Variations (15 papers) and Prenatal Screening and Diagnostics (11 papers). Samarth Bhatt is often cited by papers focused on Genomic variations and chromosomal abnormalities (18 papers), Chromosomal and Genetic Variations (15 papers) and Prenatal Screening and Diagnostics (11 papers). Samarth Bhatt collaborates with scholars based in Germany, United States and France. Samarth Bhatt's co-authors include Darlene A. Kertes, Hayley S. Kamin, Thomas Liehr, David A. Hughes, Connie J. Mulligan, Nicole C Rodney, Anja Weise, Kristin Mrasek, Sau Wai Cheung and Zhilian Xia and has published in prestigious journals such as Nature Genetics, SHILAP Revista de lepidopterología and Child Development.

In The Last Decade

Samarth Bhatt

34 papers receiving 1000 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Samarth Bhatt Germany 16 597 448 301 220 116 34 1.0k
Míriam Guitart Spain 23 914 1.5× 625 1.4× 348 1.2× 170 0.8× 185 1.6× 58 1.4k
Henrietta Szutorisz United States 18 181 0.3× 1.2k 2.6× 510 1.7× 146 0.7× 74 0.6× 24 2.0k
Ichiko Nishijima Japan 17 263 0.4× 604 1.3× 113 0.4× 88 0.4× 136 1.2× 41 1.2k
Suyinn Chong Australia 19 542 0.9× 1.2k 2.6× 692 2.3× 135 0.6× 117 1.0× 37 1.8k
Sven Bocklandt United States 13 393 0.7× 862 1.9× 165 0.5× 35 0.2× 72 0.6× 16 1.5k
Carole Samango‐Sprouse United States 24 1.2k 2.1× 846 1.9× 467 1.6× 58 0.3× 86 0.7× 71 2.0k
S G Ratcliffe United Kingdom 19 1.1k 1.9× 662 1.5× 420 1.4× 185 0.8× 127 1.1× 37 1.7k
Pille Hallast Estonia 17 382 0.6× 264 0.6× 49 0.2× 79 0.4× 68 0.6× 28 689
Akira Morishima United States 19 947 1.6× 852 1.9× 139 0.5× 235 1.1× 91 0.8× 52 1.9k
Marie‐Louise Barrenäs Sweden 21 377 0.6× 219 0.5× 96 0.3× 66 0.3× 67 0.6× 39 1.1k

Countries citing papers authored by Samarth Bhatt

Since Specialization
Citations

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

Fields of papers citing papers by Samarth Bhatt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Samarth Bhatt

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

All Works

20 of 20 papers shown
1.
Kertes, Darlene A., Nathaniel J. Hall, & Samarth Bhatt. (2018). Children’s Relationship With Their Pet Dogs and OXTR Genotype Predict Child–Pet Interaction in an Experimental Setting. Frontiers in Psychology. 9. 1472–1472. 10 indexed citations
2.
3.
Kertes, Darlene A., Hayley S. Kamin, David A. Hughes, et al.. (2015). Maternal stress predicts methylation of genes regulating the HPA axis in mothers and newborns in the Democratic Republic of Congo. Psychoneuroendocrinology. 61. 5–5. 3 indexed citations
4.
Guilherme, Roberta Santos, Mirlene Cecília Soares Pinho Cernach, S.S. Takeno, et al.. (2013). A Complex Chromosome Rearrangement Involving Four Chromosomes, Nine Breakpoints and a Cryptic 0.6-Mb Deletion in a Boy with Cerebellar Hypoplasia and Defects in Skull Ossification. Cytogenetic and Genome Research. 141(4). 317–323. 17 indexed citations
5.
6.
Bhatt, Samarth, Marina Manvelyan, Kamran Moradkhani, et al.. (2013). Inverted Segment Size and the Presence of Recombination Hot Spot Clusters Matter in Sperm Segregation Analysis. Cytogenetic and Genome Research. 142(2). 145–149. 6 indexed citations
7.
Abo-Zeid, Mona A.M., Thomas Liehr, Sherien M. El‐Daly, et al.. (2012). Molecular cytogenetic evaluation of the efficacy of photodynamic therapy by indocyanine green in breast adenocarcinoma MCF-7 cells. Photodiagnosis and Photodynamic Therapy. 10(2). 194–202. 12 indexed citations
8.
Liehr, Thomas, Jim Schröder, Monika Ziegler, et al.. (2011). Evidence for Correlation of Fragile Sites and Chromosomal Breakpoints in Carriers of Constitutional Balanced Chromosomal Rearrangements. SHILAP Revista de lepidopterología. 14(2). 13–6. 14 indexed citations
9.
Bhatt, Samarth, et al.. (2011). An unusual T-cell childhood acute lymphoblastic leukemia harboring a yet unreported near-tetraploid karyotype. Molecular Cytogenetics. 4(1). 20–20. 6 indexed citations
10.
Mkrtchyan, Hasmik, Sophie Hinreiner, Marina Manvelyan, et al.. (2010). The Human Genome Puzzle — the Role of Copy Number Variation in Somatic Mosaicism. Current Genomics. 11(6). 426–431. 30 indexed citations
11.
Shinawi, Marwan, Christian P. Schaaf, Samarth Bhatt, et al.. (2009). A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nature Genetics. 41(12). 1269–1271. 141 indexed citations
12.
Vissers, Lisenka E.L.M., Samarth Bhatt, Irene M. Janssen, et al.. (2009). Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture. Human Molecular Genetics. 18(19). 3579–3593. 114 indexed citations
13.
Liehr, Thomas, Markus Stümm, R.‐D. Wegner, et al.. (2009). 10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences. Cytogenetic and Genome Research. 124(1). 102–105. 27 indexed citations
14.
Manvelyan, Marina, Kristin Mrasek, Samarth Bhatt, et al.. (2008). Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon. Molecular Cytogenetics. 1(1). 9–9. 20 indexed citations
15.
Bhatt, Samarth, Kamran Moradkhani, Kristin Mrasek, et al.. (2008). Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. European Journal of Human Genetics. 17(1). 44–50. 14 indexed citations
16.
Bhatt, Samarth, Kamran Moradkhani, Kristin Mrasek, et al.. (2007). Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Molecular Human Reproduction. 13(10). 751–756. 15 indexed citations
17.
Moradkhani, Kamran, Jacques Puechberty, Samarth Bhatt, et al.. (2006). Meiotic segregation of rare Robertsonian translocations: sperm analysis of three t(14q;22q) cases. Human Reproduction. 21(5). 1166–1171. 19 indexed citations
18.
Moradkhani, Kamran, Jacques Puechberty, Samarth Bhatt, et al.. (2006). Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: A Case Report. Human Reproduction. 21(12). 3193–3198. 26 indexed citations
19.
Bakshi, Sonal, et al.. (2004). AML-M2 with der(18)t(1;18)(q2?;p11.3) in addition to t(8;21) and del(9q). Indian journal of human genetics. 10(2). 78. 1 indexed citations
20.
Bakshi, Sonal, et al.. (2004). Loss of sex chromosome in acute myeloid leukemia. Indian journal of human genetics. 10(1). 22. 2 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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