Moneef Shoukier

1.5k total citations
35 papers, 769 citations indexed

About

Moneef Shoukier is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Moneef Shoukier has authored 35 papers receiving a total of 769 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Genetics and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Moneef Shoukier's work include Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (4 papers) and Congenital heart defects research (4 papers). Moneef Shoukier is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Genomics and Rare Diseases (4 papers) and Congenital heart defects research (4 papers). Moneef Shoukier collaborates with scholars based in Germany, Poland and United States. Moneef Shoukier's co-authors include Csaba Poreisz, Michael A. Nitsche, Vera Moliadze, Leila Chaieb, Harald Ludwig, Andrea Antal, Kátia Monte‐Silva, Nivethida Thirugnanasambandam, Walter Paulus and Iris Bartels and has published in prestigious journals such as The Journal of Experimental Medicine, Journal of Clinical Oncology and Cancer Research.

In The Last Decade

Moneef Shoukier

35 papers receiving 708 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Moneef Shoukier Germany 15 272 237 224 155 96 35 769
William Bennett Australia 14 405 1.5× 233 1.0× 142 0.6× 81 0.5× 68 0.7× 27 911
Elizabeth Peckham United States 12 204 0.8× 228 1.0× 103 0.5× 187 1.2× 69 0.7× 19 755
Nathan C. Manley United States 13 491 1.8× 97 0.4× 160 0.7× 252 1.6× 26 0.3× 16 982
Ken‐Shiung Chen United States 13 435 1.6× 417 1.8× 34 0.2× 81 0.5× 31 0.3× 15 749
P. F. Chance United States 21 373 1.4× 170 0.7× 258 1.2× 608 3.9× 38 0.4× 28 1.1k
Maria Sundberg United States 16 797 2.9× 146 0.6× 46 0.2× 375 2.4× 84 0.9× 29 1.1k
Eeva‐Marja Sankila Finland 18 811 3.0× 198 0.8× 115 0.5× 79 0.5× 31 0.3× 38 1.1k
Maria Grazia Pomponi Italy 21 748 2.8× 662 2.8× 43 0.2× 270 1.7× 196 2.0× 56 1.2k
Melanie Willingham Australia 6 308 1.1× 53 0.2× 117 0.5× 201 1.3× 25 0.3× 6 644
Siming Shen United States 7 749 2.8× 133 0.6× 232 1.0× 217 1.4× 23 0.2× 8 1.2k

Countries citing papers authored by Moneef Shoukier

Since Specialization
Citations

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

Fields of papers citing papers by Moneef Shoukier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Moneef Shoukier

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

All Works

20 of 20 papers shown
1.
Jänne, Pasi A., Jason T. Henry, K. Papadopoulos, et al.. (2024). 503LBA LBA Orals: Results from CA240-0007, a phase 1/2 multiple expansion cohort study of BMS-986504 in patients (pts) with advanced solid tumors with homozygous MTAP deletion (MTAP-del). European Journal of Cancer. 211. 114981–114981. 2 indexed citations
2.
Haak, Monique C., Xiao Han, Martina Ruiterkamp‐Versteeg, et al.. (2024). De novo heterozygous missense variants in CELSR1 as cause of fetal pleural effusions and progressive fetal hydrops. Journal of Medical Genetics. 61(6). 549–552. 1 indexed citations
3.
Stephani, Caspar, Moneef Shoukier, Rafat Ahmed, & Claus Wolff‐Menzler. (2016). Polymorphism of the brain-derived neurotrophic factor and dynamics of the seizure threshold of electroconvulsive therapy. European Archives of Psychiatry and Clinical Neuroscience. 267(8). 787–794. 1 indexed citations
4.
Schmidt, Thomas M., Tatjana Bierhals, Fanny Kortüm, et al.. (2013). Branchio-Otic Syndrome Caused by a Genomic Rearrangement: Clinical Findings and Molecular Cytogenetic Studies in a Patient with a Pericentric Inversion of Chromosome 8. Cytogenetic and Genome Research. 142(1). 1–6. 18 indexed citations
5.
6.
Pauli, Silke, Thomas M. Schmidt, Barbara Zoll, et al.. (2012). Discordant phenotype in monozygotic twins with mosaic trisomy 12p in lymphocytes. European Journal of Medical Genetics. 55(8-9). 480–484. 9 indexed citations
7.
Pauli, Silke, Doris Steinemann, Jürgen Wienands, et al.. (2012). Occurrence of acute lymphoblastic leukemia and juvenile myelomonocytic leukemia in a patient with Noonan syndrome carrying the germline PTPN11 mutation p.E139D. American Journal of Medical Genetics Part A. 158A(3). 652–658. 10 indexed citations
8.
Shoukier, Moneef, Barbara Zoll, Peter Burfeind, et al.. (2012). A de novo interstitial deletion of 2p23.3–24.3 in a boy presenting with intellectual disability, overgrowth, dysmorphic features, skeletal myopathy, dilated cardiomyopathy. American Journal of Medical Genetics Part A. 158A(2). 429–433. 11 indexed citations
9.
Schmidt, Thomas M., Iris Bartels, Thomas Liehr, et al.. (2012). A Family with an Inverted Tandem Duplication 5q22.1q23.2. Cytogenetic and Genome Research. 139(1). 65–70. 15 indexed citations
10.
Shoukier, Moneef, Nina Klein, Bernd Auber, et al.. (2012). Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?. Clinical Genetics. 83(1). 53–65. 55 indexed citations
11.
12.
Shoukier, Moneef, Iris Bartels, Bernd Auber, et al.. (2011). A 16q12 microdeletion in a boy with severe psychomotor delay, craniofacial dysmorphism, brain and limb malformations, and a heart defect. American Journal of Medical Genetics Part A. 158A(1). 229–235. 20 indexed citations
13.
Stettner, Georg M., et al.. (2011). Familial intellectual disability and autistic behavior caused by a small FMR2 gene deletion. American Journal of Medical Genetics Part A. 155(8). 2003–2007. 20 indexed citations
14.
Lee, Jae Ho, Stefan Schweyer, Moneef Shoukier, et al.. (2010). Pathways of Proliferation and Antiapoptosis Driven in Breast Cancer Stem Cells by Stem Cell Protein Piwil2. Cancer Research. 70(11). 4569–4579. 96 indexed citations
15.
Zirn, Birgit, Larissa Arning, Iris Bartels, et al.. (2010). Ring chromosome 22 and neurofibromatosis type II: proof of two‐hit model for the loss of the NF2 gene in the development of meningioma. Clinical Genetics. 81(1). 82–87. 31 indexed citations
16.
Klimpe, Sven, Arne Zibat, Ulrich Zechner, et al.. (2010). Evaluating the effect of spastin splice mutations by quantitative allele‐specific expression assay. European Journal of Neurology. 18(1). 99–105. 6 indexed citations
17.
Antal, Andrea, Leila Chaieb, Vera Moliadze, et al.. (2010). Brain-derived neurotrophic factor (BDNF) gene polymorphisms shape cortical plasticity in humans. Brain stimulation. 3(4). 230–237. 196 indexed citations
18.
Shoukier, Moneef, et al.. (2008). Expansion of mutation spectrum, determination of mutation cluster regions and predictive structural classification of SPAST mutations in hereditary spastic paraplegia. European Journal of Human Genetics. 17(2). 187–194. 67 indexed citations
19.
Wirbelauer, Johannes, et al.. (2008). A newborn with hereditary haemorrhagic telangiectasia and an unusually severe phenotype. Swiss Medical Weekly. 138(2930). 432–435. 2 indexed citations
20.
Shoukier, Moneef, et al.. (2008). Characterization of five novel large deletions causing hereditary haemorrhagic telangiectasia. Clinical Genetics. 73(4). 320–330. 10 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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