Samin A. Sajan

1.3k total citations
17 papers, 816 citations indexed

About

Samin A. Sajan is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Samin A. Sajan has authored 17 papers receiving a total of 816 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 8 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Samin A. Sajan's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (5 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Samin A. Sajan is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (5 papers) and Hearing, Cochlea, Tinnitus, Genetics (3 papers). Samin A. Sajan collaborates with scholars based in United States, France and Japan. Samin A. Sajan's co-authors include Michael Lovett, Mark E. Warchol, R. David Hawkins, Brian C. Schutte, Christopher R. Ingraham, Akira Kinoshita, Shinji Kondo, Jeffrey C. Murray, Martine Dunnwald and Baoli Yang and has published in prestigious journals such as Nature Genetics, PLoS ONE and Genetics.

In The Last Decade

Samin A. Sajan

17 papers receiving 785 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Samin A. Sajan United States	13	424	422	99	95	63	17	816
Hyung‐Goo Kim United States	19	715 1.7×	683 1.6×	45 0.5×	65 0.7×	73 1.2×	68	1.4k
Ewa Obersztyn Poland	19	692 1.6×	711 1.7×	61 0.6×	40 0.4×	130 2.1×	78	1.2k
Philippe Vago France	20	422 1.0×	297 0.7×	262 2.6×	137 1.4×	146 2.3×	89	1.2k
Derek Silvius United States	11	981 2.3×	252 0.6×	206 2.1×	89 0.9×	82 1.3×	18	1.3k
Buffy S. Ellsworth United States	14	571 1.3×	345 0.8×	49 0.5×	106 1.1×	34 0.5×	29	937
Carolina Parada United States	21	890 2.1×	460 1.1×	74 0.7×	79 0.8×	84 1.3×	24	1.3k
M. Mark Taketo Japan	15	1.0k 2.4×	452 1.1×	181 1.8×	86 0.9×	17 0.3×	17	1.4k
Shanru Li United States	20	812 1.9×	256 0.6×	63 0.6×	156 1.6×	22 0.3×	26	1.4k
Dan Zou United States	7	466 1.1×	127 0.3×	146 1.5×	43 0.5×	40 0.6×	9	677
Mark‐Oliver Trowe Germany	15	795 1.9×	116 0.3×	117 1.2×	66 0.7×	70 1.1×	26	964

Countries citing papers authored by Samin A. Sajan

Since Specialization

Citations

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

Fields of papers citing papers by Samin A. Sajan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Samin A. Sajan. 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 Samin A. Sajan. The network helps show where Samin A. Sajan may publish in the future.

Co-authorship network of co-authors of Samin A. Sajan

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

All Works

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17 of 17 papers shown

Sajan, Samin A., Carolyn M. Brown, Laura Davis‐Keppen, et al.. (2023). The smallest likely pathogenic duplication of a SOX9 enhancer identified to date in a family with 46,XX testicular differences of sex development. American Journal of Medical Genetics Part A. 191(12). 2831–2836. 3 indexed citations

Powis, Zöe, Meghan C. Towne, Kelly D. Farwell Hagman, et al.. (2019). Clinical diagnostic exome sequencing in dystonia: Genetic testing challenges for complex conditions. Clinical Genetics. 97(2). 305–311. 21 indexed citations

Smith, Erica D., Kirsten Blanco, Samin A. Sajan, et al.. (2019). A retrospective review of multiple findings in diagnostic exome sequencing: halF.A.re distinct and halF.A.re overlapping diagnoses. Genetics in Medicine. 21(10). 2199–2207. 61 indexed citations

Sajan, Samin A., Zöe Powis, Katherine L. Helbig, et al.. (2018). Diagnostic exome sequencing identifies GLI 2 haploinsufficiency and chromosome 20 uniparental disomy in a patient with developmental anomalies. Clinical Case Reports. 6(7). 1208–1213. 3 indexed citations

Sajan, Samin A., Jaya Ganesh, Deepali N. Shinde, et al.. (2018). Biallelic disruption of PKDCC is associated with a skeletal disorder characterised by rhizomelic shortening of extremities and dysmorphic features. Journal of Medical Genetics. 56(12). 850–854. 14 indexed citations

Helbig, Katherine L., Cameron Mroske, Denish Moorthy, Samin A. Sajan, & Milen Velinov. (2017). Biallelic loss‐of‐function variants in DOCK3 cause muscle hypotonia, ataxia, and intellectual disability. Clinical Genetics. 92(4). 430–433. 18 indexed citations

Hagman, Kelly D. Farwell, Deepali N. Shinde, Cameron Mroske, et al.. (2016). Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in Medicine. 19(2). 224–235. 34 indexed citations

Sajan, Samin A., Shalini N. Jhangiani, Donna M. Muzny, et al.. (2016). Enrichment of mutations in chromatin regulators in people with Rett syndrome lacking mutations in MECP2. Genetics in Medicine. 19(1). 13–19. 53 indexed citations

Paciorkowski, Alex R., Kim M. Keppler‐Noreuil, Luther K. Robinson, et al.. (2013). Deletion 16p13.11 uncovers NDE1 mutations on the non‐deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption. American Journal of Medical Genetics Part A. 161(7). 1523–1530. 60 indexed citations

10.

Sajan, Samin A., Liliana Fernández, Sahar Esmaeeli Nieh, et al.. (2013). Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria. PLoS Genetics. 9(10). e1003823–e1003823. 62 indexed citations

11.

Sajan, Samin A. & R. David Hawkins. (2012). Methods for Identifying Higher-Order Chromatin Structure. Annual Review of Genomics and Human Genetics. 13(1). 59–82. 53 indexed citations

12.

Sajan, Samin A., John L.R. Rubenstein, Mark E. Warchol, & Michael Lovett. (2011). Identification of direct downstream targets of Dlx5 during early inner ear development. Human Molecular Genetics. 20(7). 1262–1273. 26 indexed citations

13.

Sajan, Samin A., et al.. (2010). Novel Approaches to Studying the Genetic Basis of Cerebellar Development. The Cerebellum. 9(3). 272–283. 12 indexed citations

14.

Bashiardes, Stavros, Kara E. Powder, Samin A. Sajan, et al.. (2007). Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia. PLoS ONE. 2(6). e525–e525. 63 indexed citations

15.

Sajan, Samin A., Mark E. Warchol, & Michael Lovett. (2007). Toward a Systems Biology of Mouse Inner Ear Organogenesis: Gene Expression Pathways, Patterns and Network Analysis. Genetics. 177(1). 631–653. 48 indexed citations

16.

Ingraham, Christopher R., Akira Kinoshita, Shinji Kondo, et al.. (2006). Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6). Nature Genetics. 38(11). 1335–1340. 275 indexed citations

17.

Taylor, Ann & Samin A. Sajan. (2005). Testing for Genetically Modified Foods Using PCR. Journal of Chemical Education. 82(4). 597–597. 10 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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