Hiba Risheg

1.1k total citations
13 papers, 640 citations indexed

About

Hiba Risheg is a scholar working on Molecular Biology, Genetics and Rheumatology. According to data from OpenAlex, Hiba Risheg has authored 13 papers receiving a total of 640 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Rheumatology. Recurrent topics in Hiba Risheg's work include Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (6 papers) and Porphyrin Metabolism and Disorders (4 papers). Hiba Risheg is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Congenital heart defects research (6 papers) and Porphyrin Metabolism and Disorders (4 papers). Hiba Risheg collaborates with scholars based in United States, Qatar and Australia. Hiba Risheg's co-authors include Rachel D. Burnside, Romela Pasion, Stuart Schwartz, Vikram Jaswaney, Inder Gadi, Joseph R. Bloomer, Peter Papenhausen, James Tepperberg, Elisabeth A. Keitges and Janice Smith and has published in prestigious journals such as Nature Genetics, Human Genetics and Journal of Pediatric Gastroenterology and Nutrition.

In The Last Decade

Hiba Risheg

13 papers receiving 588 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hiba Risheg United States 10 403 374 164 53 44 13 640
Mónica Rosello Spain 14 360 0.9× 295 0.8× 95 0.6× 47 0.9× 33 0.8× 41 535
Joanna Wiszniewska United States 12 360 0.9× 348 0.9× 106 0.6× 67 1.3× 36 0.8× 22 607
J. Edward Spence United States 15 615 1.5× 527 1.4× 361 2.2× 82 1.5× 30 0.7× 23 959
Roel Hordijk Netherlands 15 520 1.3× 409 1.1× 184 1.1× 100 1.9× 35 0.8× 22 739
Tracy Brandt United States 10 399 1.0× 286 0.8× 82 0.5× 35 0.7× 26 0.6× 14 581
Nicole Maas Belgium 7 351 0.9× 191 0.5× 101 0.6× 120 2.3× 31 0.7× 13 455
Josephine Wincent Sweden 12 214 0.5× 243 0.6× 66 0.4× 55 1.0× 23 0.5× 19 467
Sonia Nizard France 10 227 0.6× 131 0.4× 87 0.5× 21 0.4× 17 0.4× 12 357
Ho‐Ming Luk China 13 267 0.7× 249 0.7× 100 0.6× 19 0.4× 14 0.3× 67 471
Shehla Mohammed United Kingdom 12 248 0.6× 497 1.3× 54 0.3× 43 0.8× 19 0.4× 25 680

Countries citing papers authored by Hiba Risheg

Since Specialization
Citations

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

Fields of papers citing papers by Hiba Risheg

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hiba Risheg

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

All Works

13 of 13 papers shown
1.
Risheg, Hiba, et al.. (2017). Response to Growth Hormone Treatment in a Patient with Insulin-Like Growth Factor 1 Receptor Deletion. Journal of Clinical Research in Pediatric Endocrinology. 9(4). 380–386. 7 indexed citations
2.
Cheng, Andrew, Mary Beth Dinulos, Whitney Neufeld‐Kaiser, et al.. (2017). 6q25.1 (TAB2) microdeletion syndrome: Congenital heart defects and cardiomyopathy. American Journal of Medical Genetics Part A. 173(7). 1848–1857. 30 indexed citations
3.
Yelavarthi, Krishna K., Golder N. Wilson, Luis Rohena, et al.. (2015). Partial monosomy of 11q22.2q22.3 including the SDHD gene in individuals with developmental delay. American Journal of Medical Genetics Part A. 167(4). 695–700. 2 indexed citations
4.
Keitges, Elisabeth A., Romela Pasion, Rachel D. Burnside, et al.. (2013). Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects. American Journal of Medical Genetics Part A. 161(7). 1755–1758. 28 indexed citations
5.
Burnside, Rachel D., John Pappas, Stephanie Sacharow, et al.. (2013). Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype. American Journal of Medical Genetics Part A. 161(4). 822–828. 30 indexed citations
6.
Risheg, Hiba, Romela Pasion, Virginia K. Proud, et al.. (2013). Clinical Comparison of Overlapping Deletions of 19p13.3. American Journal of Medical Genetics Part A. 161(5). 1110–1116. 9 indexed citations
7.
Burnside, Rachel D., Romela Pasion, Fady M. Mikhail, et al.. (2011). Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay. Human Genetics. 130(4). 517–528. 182 indexed citations
8.
Papenhausen, Peter, Stuart Schwartz, Hiba Risheg, et al.. (2011). UPD detection using homozygosity profiling with a SNP genotyping microarray. American Journal of Medical Genetics Part A. 155(4). 757–768. 115 indexed citations
9.
Risheg, Hiba, John M. Graham, Robin D. Clark, et al.. (2007). A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome. Nature Genetics. 39(4). 451–453. 152 indexed citations
10.
Bloomer, Joseph R., Yongming Wang, Anuj Singhal, & Hiba Risheg. (2006). Biochemical Abnormality in Erythropoietic Protoporphyria. Journal of Pediatric Gastroenterology and Nutrition. 43(S1). S36–40. 5 indexed citations
11.
Bloomer, Joseph R., Yongming Wang, Anuj Singhal, & Hiba Risheg. (2005). Molecular Studies of Liver Disease in Erythropoietic Protoporphyria. Journal of Clinical Gastroenterology. 39(4). S167–S175. 21 indexed citations
12.
Risheg, Hiba, et al.. (2003). Genotypic determinants of phenotype in North American patients with erythropoietic protoporphyria. Molecular Genetics and Metabolism. 80(1-2). 196–206. 25 indexed citations
13.
Risheg, Hiba, et al.. (2002). Ferrochelatase gene mutations in erythropoietic protoporphyria: focus on liver disease.. PubMed. 48(1). 83–9. 34 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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