Sansnee Chatkupt

883 total citations
18 papers, 616 citations indexed

About

Sansnee Chatkupt is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Sansnee Chatkupt has authored 18 papers receiving a total of 616 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Surgery. Recurrent topics in Sansnee Chatkupt's work include Genetic Syndromes and Imprinting (4 papers), Folate and B Vitamins Research (4 papers) and Prenatal Screening and Diagnostics (3 papers). Sansnee Chatkupt is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Folate and B Vitamins Research (4 papers) and Prenatal Screening and Diagnostics (3 papers). Sansnee Chatkupt collaborates with scholars based in United States, Netherlands and India. Sansnee Chatkupt's co-authors include William G. Johnson, M. Richard Koenigsberger, Edward S. Stenroos, Steven Buyske, Leo Wolansky, Charles Searby, Victor Ionâşescu, R. Ionasescu, Ben C.J. Hamel and Frans A. Hol and has published in prestigious journals such as Neurology, American Journal of Roentgenology and Journal of the Neurological Sciences.

In The Last Decade

Sansnee Chatkupt

18 papers receiving 601 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sansnee Chatkupt United States	13	267	215	165	144	108	18	616
Chirane Viseskul United States	15	227 0.9×	54 0.3×	167 1.0×	180 1.3×	152 1.4×	31	615
Mauro Buscaglia Italy	15	173 0.6×	36 0.2×	520 3.2×	89 0.6×	80 0.7×	24	911
Felicity Collins Australia	16	406 1.5×	127 0.6×	133 0.8×	326 2.3×	23 0.2×	22	760
Melissa Maisenbacher United States	17	511 1.9×	70 0.3×	331 2.0×	401 2.8×	147 1.4×	33	1.0k
B.M. Lippe United States	10	501 1.9×	31 0.1×	243 1.5×	448 3.1×	114 1.1×	16	1.1k
Joanne Mackey United States	12	133 0.5×	439 2.0×	59 0.4×	74 0.5×	80 0.7×	16	781
J E Wraith United Kingdom	11	92 0.3×	192 0.9×	34 0.2×	61 0.4×	35 0.3×	12	740
Jean‐Michel Pedespan France	15	145 0.5×	35 0.2×	197 1.2×	121 0.8×	59 0.5×	34	536
Linda Gailīte Latvia	12	155 0.6×	46 0.2×	68 0.4×	142 1.0×	36 0.3×	67	437
Ed Wraith United Kingdom	11	149 0.6×	203 0.9×	63 0.4×	69 0.5×	49 0.5×	24	910

Countries citing papers authored by Sansnee Chatkupt

Since Specialization

Citations

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

Fields of papers citing papers by Sansnee Chatkupt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sansnee Chatkupt

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

All Works

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18 of 18 papers shown

Johnson, William G., et al.. (2003). New 19 bp deletion polymorphism in intron‐1 of dihydrofolate reductase (DHFR): A risk factor for spina bifida acting in mothers during pregnancy?. American Journal of Medical Genetics Part A. 124A(4). 339–345. 118 indexed citations

Johnson, William G., Edward S. Stenroos, Simon Heath, et al.. (1999). Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifida. American Journal of Medical Genetics. 87(5). 407–412. 14 indexed citations

Vu, Tuan, Monica Sciacco, Kurenai Tanji, et al.. (1998). Clinical manifestations of mitochondria1 DNA depletion. Neurology. 50(6). 1783–1790. 91 indexed citations

Ionâşescu, Victor, et al.. (1997). Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene. Muscle & Nerve. 20(1). 97–99. 59 indexed citations

Hol, Frans A., M.P.A. Geurds, Sansnee Chatkupt, et al.. (1996). PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.. Journal of Medical Genetics. 33(8). 655–660. 52 indexed citations

Chatkupt, Sansnee, et al.. (1995). Spinocerebellar degeneration and cerebral hypomyelination in a family. American Journal of Medical Genetics. 60(3). 188–191. 1 indexed citations

Wolansky, Leo, et al.. (1995). Subacute combined degeneration of the spinal cord: MRI detection of preferential involvement of the posterior columns in a child. Pediatric Radiology. 25(2). 140–141. 29 indexed citations

Johnson, William G., et al.. (1995). Reduced fecundity in male ALS gene‐carriers. American Journal of Medical Genetics. 59(2). 149–153. 8 indexed citations

Chatkupt, Sansnee, et al.. (1995). Parents do matter: genomic imprinting and parental sex effects in neurological disorders. Journal of the Neurological Sciences. 130(1). 1–10. 12 indexed citations

10.

Chatkupt, Sansnee, Frans A. Hol, Yin Yao Shugart, et al.. (1995). Absence of linkage between familial neural tube defects and PAX3 gene.. Journal of Medical Genetics. 32(3). 200–204. 25 indexed citations

11.

Chatkupt, Sansnee, Marcy C. Speer, Marc A. Thomas, et al.. (1994). Linkage analysis of a candidate locus (HLA) in autosomal dominant sacral defect with anterior meningocele. American Journal of Medical Genetics. 52(1). 1–4. 9 indexed citations

12.

Chatkupt, Sansnee, et al.. (1994). Study of genetics, epidemiology, and vitamin usage in familial spina bifida in the United States in the 1990s. Neurology. 44(1). 65–65. 36 indexed citations

13.

Allitto, Bernice A., L. Michaud, Sansnee Chatkupt, et al.. (1994). Paternal isodisomy for chromosome 5 in a child with spinal muscular atrophy.. PubMed. 54(3). 482–8. 36 indexed citations

14.

Chatkupt, Sansnee & William G. Johnson. (1993). Waardenburg syndrome and myelomeningocele in a family.. Journal of Medical Genetics. 30(1). 83–84. 35 indexed citations

15.

Chatkupt, Sansnee, et al.. (1993). Characteristic MR findings in a neonate with incontinentia pigmenti.. American Journal of Roentgenology. 160(2). 372–374. 28 indexed citations

16.

Chatkupt, Sansnee, et al.. (1993). Antepartum diagnosis of discordant anencephaly in dicephalic conjoined twins. Journal of Clinical Ultrasound. 21(2). 138–142. 5 indexed citations

17.

Chatkupt, Sansnee, et al.. (1992). Parental sex effect in spina bifida: A role for genomic imprinting?. American Journal of Medical Genetics. 44(4). 508–512. 40 indexed citations

18.

Chatkupt, Sansnee, et al.. (1987). Cerebellar infarction in children. Pediatric Neurology. 3(6). 363–366. 18 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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