Neda Zadeh

1.1k total citations
12 papers, 253 citations indexed

About

Neda Zadeh is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Neda Zadeh has authored 12 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Surgery, 5 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Neda Zadeh's work include Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers) and Epigenetics and DNA Methylation (2 papers). Neda Zadeh is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetic Syndromes and Imprinting (3 papers) and Epigenetics and DNA Methylation (2 papers). Neda Zadeh collaborates with scholars based in United States, Israel and Germany. Neda Zadeh's co-authors include Wayne W. Grody, Louanne Hudgins, Terri Getzug, Andrea Kwan, Melanie A. Manning, M. Carrie Miceli, Éric Vilain, Stanley F. Nelson, Joshua L. Deignan and Samuel P. Strom and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Genetics in Medicine.

In The Last Decade

Neda Zadeh

11 papers receiving 251 citations

Peers

Neda Zadeh

GENET

PPCH

SURGE

PRM

Milena Simioni Brazil

María Gabriela Obregón Argentina

Lavinia Caba Romania

Stefano Petrocchi Italy

Cara Skraban United States

Koen Devriendt Belgium

Chiara Castronovo Italy

Renqian Du China

Özlem Akgün Doğan Türkiye

N. Logghe Belgium

Milena Simioni Brazil

Neda Zadeh

125 ×0.8

195 ×1.4

GENET

33 ×1.2

PPCH

20 ×0.8

SURGE

37 ×1.9

PRM

Citations per year, relative to Neda Zadeh Neda Zadeh (= 1×) peers Milena Simioni

Countries citing papers authored by Neda Zadeh

Since Specialization

Citations

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

Fields of papers citing papers by Neda Zadeh

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neda Zadeh

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

All Works

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12 of 12 papers shown

Halnon, Nancy, et al.. (2025). Cardiac pathology in a patient with a novel pathogenic variant c.703del (p.Ile235SerfsTer4) of the TAFAZZIN gene. Cardiovascular Pathology. 79. 107749–107749. 1 indexed citations

Zadeh, Neda, et al.. (2023). Congenital myasthenic syndrome type 2C in a neonate: Redefining the phenotype of CHRNB1‐related myasthenic syndromes. SHILAP Revista de lepidopterología. 1(4). 324–326.

Batzir, Nurit Assia, Jennifer E. Posey, Xiaofei Song, et al.. (2019). Phenotypic expansion of POGZ‐related intellectual disability syndrome (White‐Sutton syndrome). American Journal of Medical Genetics Part A. 182(1). 38–52. 30 indexed citations

Zadeh, Neda & John M. Graham. (2017). KCNK9 Imprinting Syndrome. Europe PMC (PubMed Central). 1 indexed citations

Graham, John M., Neda Zadeh, Ee Shien Tan, et al.. (2016). KCNK9 imprinting syndrome—further delineation of a possible treatable disorder. American Journal of Medical Genetics Part A. 170(10). 2632–2637. 26 indexed citations

Arboleda, Valerie A., Hane Lee, Naghmeh Dorrani, et al.. (2015). De Novo Nonsense Mutations in KAT6A, a Lysine Acetyl-Transferase Gene, Cause a Syndrome Including Microcephaly and Global Developmental Delay. The American Journal of Human Genetics. 96(3). 498–506. 92 indexed citations

Brennan, Marie‐Luise, Margaret P Adam, Laurie H. Seaver, et al.. (2014). Increased body mass in infancy and early toddlerhood in Angelman syndrome patients with uniparental disomy and imprinting center defects. American Journal of Medical Genetics Part A. 167(1). 142–146. 14 indexed citations

Lionetti, Geraldina, Jonathan A. Bernstein, Dirk Holzinger, et al.. (2012). IL-1 blockade as a novel approach to treatment of hyperzincemia and hypercalprotectinemia, a possible new autoinflammatory syndrome. Pediatric Rheumatology. 10(S1). 1 indexed citations

Zadeh, Neda, Terri Getzug, & Wayne W. Grody. (2011). Diagnosis and management of familial Mediterranean fever: Integrating medical genetics in a dedicated interdisciplinary clinic. Genetics in Medicine. 13(3). 263–269. 38 indexed citations

10.

Zadeh, Neda, Jonathan A. Bernstein, Sarah Dugan, et al.. (2011). Ectopia lentis as the presenting and primary feature in Marfan syndrome. American Journal of Medical Genetics Part A. 155(11). 2661–2668. 35 indexed citations

11.

Zadeh, Neda, Louanne Hudgins, & Mary E. Norton. (2011). Nuchal translucency measurement in fetuses with spinal muscular atrophy. Prenatal Diagnosis. 31(4). 327–330. 12 indexed citations

12.

Zadeh, Neda & Louanne Hudgins. (2009). The Genetic Approach to Hypotonia in the Neonate. NeoReviews. 10(12). e600–e607. 3 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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