Amira Masri

1.5k total citations
6 papers, 169 citations indexed

About

Amira Masri is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Physiology. According to data from OpenAlex, Amira Masri has authored 6 papers receiving a total of 169 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Pediatrics, Perinatology and Child Health and 2 papers in Physiology. Recurrent topics in Amira Masri's work include Prenatal Screening and Diagnostics (2 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Lysosomal Storage Disorders Research (2 papers). Amira Masri is often cited by papers focused on Prenatal Screening and Diagnostics (2 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Lysosomal Storage Disorders Research (2 papers). Amira Masri collaborates with scholars based in Jordan, United States and France. Amira Masri's co-authors include Hanan Hamamy, Azmy M. Al-Hadidy, Ling Ling, Stanley F. Nelson, Bruno Reversade, Mohammad Shboul, Jing Tian, Brian D. O’Connor, Hane Lee and Osama H. Ababneh and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Molecular Genetics and Metabolism.

In The Last Decade

Amira Masri

6 papers receiving 164 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Amira Masri Jordan	5	96	49	48	44	16	6	169
Zejuan Sheng United States	8	286 3.0×	42 0.9×	54 1.1×	61 1.4×	9 0.6×	10	340
Jean-Louis Dufier France	7	173 1.8×	61 1.2×	33 0.7×	18 0.4×	10 0.6×	8	288
Gertrud Strobl‐Wildemann Germany	6	97 1.0×	74 1.5×	75 1.6×	59 1.3×	5 0.3×	7	215
Christopher Elzinga United States	5	58 0.6×	37 0.8×	106 2.2×	18 0.4×	10 0.6×	5	186
Cathryn Poulton Netherlands	5	138 1.4×	108 2.2×	27 0.6×	63 1.4×	7 0.4×	5	266
Marianne McGuire United States	8	173 1.8×	100 2.0×	68 1.4×	13 0.3×	9 0.6×	11	262
Ruobing Zou Canada	5	146 1.5×	40 0.8×	131 2.7×	18 0.4×	7 0.4×	5	221
Carolin Walter Germany	8	181 1.9×	40 0.8×	41 0.9×	20 0.5×	35 2.2×	30	312
Thomas Smol France	10	129 1.3×	70 1.4×	17 0.4×	22 0.5×	14 0.9×	34	224
Pierre Ougen France	6	157 1.6×	91 1.9×	51 1.1×	32 0.7×	24 1.5×	7	237

Countries citing papers authored by Amira Masri

Since Specialization

Citations

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

Fields of papers citing papers by Amira Masri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amira Masri

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

All Works

Sort: Min cites: Since: Top N: Style:

6 of 6 papers shown

1.

Zaki, Maha S., Amira Masri, Anne Gregor, Joseph G. Gleeson, & Rasim Özgür Rosti. (2015). Dandy–Walker malformation, genitourinary abnormalities, and intellectual disability in two families. American Journal of Medical Genetics Part A. 167(11). 2503–2507. 4 indexed citations

2.

Masri, Amira, Stefania Gimelli, Hanan Hamamy, & Frédérique Sloan‐Béna. (2014). Microarray delineation of familial chromosomal imbalance with deletion 5q35 and duplication 10q25 in a child showing multiple anomalies and dysmorphism. American Journal of Medical Genetics Part A. 164(5). 1254–1261. 3 indexed citations

3.

Hills, L. Benjamin, Amira Masri, Wataru Kakegawa, et al.. (2013). Deletions in GRID2 lead to a recessive syndrome of cerebellar ataxia and tonic upgaze in humans. Neurology. 81(16). 1378–1386. 71 indexed citations

4.

Haghighi, Alireza, Amira Masri, Ruth Kornreich, & Robert J. Desnick. (2011). Tay-Sachs disease in an Arab family due to c.78G>A HEXA nonsense mutation encoding a p.W26X early truncation enzyme peptide. Molecular Genetics and Metabolism. 104(4). 700–702. 4 indexed citations

5.

Tian, Jing, Ling Ling, Mohammad Shboul, et al.. (2010). Loss of CHSY1, a Secreted FRINGE Enzyme, Causes Syndromic Brachydactyly in Humans via Increased NOTCH Signaling. The American Journal of Human Genetics. 87(6). 768–778. 65 indexed citations

6.

Masri, Amira, Faris G. Bakri, Maysa Al‐Hussaini, et al.. (2008). Griscelli Syndrome Type 2: A Rare and Lethal Disorder. Journal of Child Neurology. 23(8). 964–967. 22 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.

Explore authors with similar magnitude of impact