Naomi Yachelevich

879 total citations
6 papers, 33 citations indexed

About

Naomi Yachelevich is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Naomi Yachelevich has authored 6 papers receiving a total of 33 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Physiology. Recurrent topics in Naomi Yachelevich's work include Genetic Syndromes and Imprinting (1 paper), Congenital limb and hand anomalies (1 paper) and Hedgehog Signaling Pathway Studies (1 paper). Naomi Yachelevich is often cited by papers focused on Genetic Syndromes and Imprinting (1 paper), Congenital limb and hand anomalies (1 paper) and Hedgehog Signaling Pathway Studies (1 paper). Naomi Yachelevich collaborates with scholars based in United States, Sweden and Denmark. Naomi Yachelevich's co-authors include Gilad D. Evrony, Julia Gittler, Sarah L. Nolin, Carl Dobkin, John Pappas, Kim Henriksen, Susan Sklower Brooks, Brenda Kohn, Ilana Moscatelli and Leena Ala‐Kokko and has published in prestigious journals such as Molecular Genetics and Metabolism, American Journal of Medical Genetics Part A and Current problems in pediatric and adolescent health care.

In The Last Decade

Naomi Yachelevich

6 papers receiving 32 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Naomi Yachelevich United States	5	20	19	4	4	4	6	33
Randa Bassiouni Egypt	4	15 0.8×	19 1.0×	9 2.3×	12 3.0×	4 1.0×	7	36
Andrea Seeley United States	5	31 1.6×	17 0.9×	13 3.3×	2 0.5×	4 1.0×	8	57
Francesca Inzana Italy	3	27 1.4×	18 0.9×	8 2.0×	2 0.5×		3	39
Nikolay Plotnikov Russia	4	17 0.8×	12 0.6×	2 0.5×	4 1.0×	12 3.0×	14	46
Joe Nadeau Germany	3	24 1.2×	18 0.9×	5 1.3×		2 0.5×	3	36
Angela Hobbs South Africa	4	6 0.3×	18 0.9×	2 0.5×	5 1.3×	6 1.5×	5	35
Friedhelm Hildebrandt United States	3	18 0.9×	23 1.2×	4 1.0×	2 0.5×		4	29
Sharon L. R. Kardia United States	3	47 2.4×	25 1.3×	2 0.5×	3 0.8×	2 0.5×	3	65
Catriona L. K. Barnes France	3	17 0.8×	9 0.5×	1 0.3×	2 0.5×	2 0.5×	4	32
Samuel H. Zinner United States	2	20 1.0×	17 0.9×	5 1.3×	3 0.8×		2	33

Countries citing papers authored by Naomi Yachelevich

Since Specialization

Citations

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

Fields of papers citing papers by Naomi Yachelevich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Naomi Yachelevich

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

All Works

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6 of 6 papers shown

1.

Yachelevich, Naomi, et al.. (2021). Genotype - phenotype correlation in an adolescent girl with pathogenic PPARy genetic variation that caused severe hypertriglyceridemia and early onset type 2 diabetes. Annals of Pediatric Endocrinology & Metabolism. 26(4). 284–289. 4 indexed citations

2.

Yachelevich, Naomi, et al.. (2020). Transcriptome sequencing identifies a noncoding, deep intronic variant in CLCN7 causing autosomal recessive osteopetrosis. Molecular Genetics & Genomic Medicine. 8(10). e1405–e1405. 7 indexed citations

3.

Lau, Heather, Swapnil Parmar, Mikhail Kazachkov, et al.. (2016). Enzyme replacement therapy with investigational rhGUS in an infant with non-immune hydrops fetalis and mucopolysaccharidosis type VII. Molecular Genetics and Metabolism. 117(2). S71–S71. 3 indexed citations

4.

Yachelevich, Naomi. (2015). Generalized Overgrowth Syndromes With Prenatal Onset. Current problems in pediatric and adolescent health care. 45(4). 97–111. 7 indexed citations

5.

Yachelevich, Naomi, Julia Gittler, Susan Klugman, et al.. (2011). Terminal deletions of the long arm of chromosome X that include the FMR1 gene in female patients: A case series. American Journal of Medical Genetics Part A. 155(4). 870–874. 7 indexed citations

6.

Shanske, Alan, Naomi Yachelevich, Leena Ala‐Kokko, Jay Leonard, & Brynn Levy. (2009). Wolf–Hirschhorn syndrome and ectrodactyly: New findings and a review of the literature. American Journal of Medical Genetics Part A. 152A(1). 203–208. 5 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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