Sunita Katari

848 total citations
8 papers, 629 citations indexed

About

Sunita Katari is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Sunita Katari has authored 8 papers receiving a total of 629 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Pediatrics, Perinatology and Child Health, 4 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in Sunita Katari's work include Genetic Syndromes and Imprinting (4 papers), Prenatal Screening and Diagnostics (4 papers) and Epigenetics and DNA Methylation (3 papers). Sunita Katari is often cited by papers focused on Genetic Syndromes and Imprinting (4 papers), Prenatal Screening and Diagnostics (4 papers) and Epigenetics and DNA Methylation (3 papers). Sunita Katari collaborates with scholars based in United States. Sunita Katari's co-authors include Carmen Sapienza, Nahid Turan, Christos Coutifaris, Michael Foster, Raffi Chalian, Marina Bibikova, John P. Gaughan, John Gaughan, Mohamed Ghalwash and Zoran Obradović and has published in prestigious journals such as Human Molecular Genetics, PLoS Genetics and Biology of Reproduction.

In The Last Decade

Sunita Katari

7 papers receiving 604 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sunita Katari United States	7	423	297	204	129	94	8	629
Galyna Pliushch Germany	8	320 0.8×	394 1.3×	212 1.0×	62 0.5×	158 1.7×	8	577
Naama Srebnik Israel	15	220 0.5×	69 0.2×	113 0.6×	247 1.9×	82 0.9×	39	475
A. Zimon United States	7	129 0.3×	76 0.3×	114 0.6×	81 0.6×	47 0.5×	14	327
H Lehnen Germany	9	458 1.1×	282 0.9×	88 0.4×	53 0.4×	368 3.9×	20	675
J. Closset Belgium	7	158 0.4×	94 0.3×	138 0.7×	92 0.7×	116 1.2×	13	558
C. Rongen‐Westerlaken Netherlands	14	190 0.4×	464 1.6×	529 2.6×	37 0.3×	42 0.4×	23	817
Eduardo Chaler Argentina	13	113 0.3×	244 0.8×	198 1.0×	48 0.4×	18 0.2×	29	583
Felix Schreiner Germany	13	111 0.3×	215 0.7×	215 1.1×	60 0.5×	26 0.3×	35	546
Alexander Drong United Kingdom	7	96 0.2×	356 1.2×	132 0.6×	53 0.4×	57 0.6×	10	530
Annamaria Baggiani Italy	14	343 0.8×	98 0.3×	47 0.2×	253 2.0×	195 2.1×	32	665

Countries citing papers authored by Sunita Katari

Since Specialization

Citations

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

Fields of papers citing papers by Sunita Katari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sunita Katari

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

All Works

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8 of 8 papers shown

1.

Turan, Nahid, Mohamed Ghalwash, Sunita Katari, et al.. (2012). DNA methylation differences at growth related genes correlate with birth weight: a molecular signature linked to developmental origins of adult disease?. BMC Medical Genomics. 5(1). 10–10. 86 indexed citations

2.

Turan, Nahid, Sunita Katari, Christos Coutifaris, & Carmen Sapienza. (2010). Explaining inter-individual variability in phenotype: Is epigenetics up to the challenge?. Epigenetics. 5(1). 16–19. 40 indexed citations

3.

Turan, Nahid, Sunita Katari, Raffi Chalian, et al.. (2010). Inter- and Intra-Individual Variation in Allele-Specific DNA Methylation and Gene Expression in Children Conceived using Assisted Reproductive Technology. PLoS Genetics. 6(7). e1001033–e1001033. 136 indexed citations

4.

Katari, Sunita, Nahid Turan, Marina Bibikova, et al.. (2009). DNA methylation and gene expression differences in children conceived in vitro or in vivo. Human Molecular Genetics. 18(20). 3769–3778. 327 indexed citations

5.

Grotegut, Chad A., et al.. (2008). Obstetric outcomes with a false-positive one-hour glucose challenge test by the Carpenter-Coustan criteria. The Journal of Maternal-Fetal & Neonatal Medicine. 21(5). 315–320. 10 indexed citations

6.

Turan, Nahid, et al.. (2008). Inter- and Intra-individual Variation in Allele-specific DNA Methylation.. Biology of Reproduction. 78(Suppl_1). 192–192.

7.

Grotegut, Chad A., et al.. (2006). Baking soda pica: a case of hypokalemic metabolic alkalosis and rhabdomyolysis in pregnancy.. PubMed. 107(2 Pt 2). 484–6. 22 indexed citations

8.

Grotegut, Chad A., et al.. (2006). Obstetric Outcomes in Pregnancies Complicated by a False–Positive One-Hour Glucose Challenge Test. Obstetrics and Gynecology. 107(Supplement). 96S–96S. 8 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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