Mark Hannibal

5.3k total citations
48 papers, 1.7k citations indexed

About

Mark Hannibal is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Mark Hannibal has authored 48 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 16 papers in Molecular Biology and 12 papers in Immunology. Recurrent topics in Mark Hannibal's work include Connective tissue disorders research (6 papers), HIV Research and Treatment (6 papers) and Immune Cell Function and Interaction (6 papers). Mark Hannibal is often cited by papers focused on Connective tissue disorders research (6 papers), HIV Research and Treatment (6 papers) and Immune Cell Function and Interaction (6 papers). Mark Hannibal collaborates with scholars based in United States, New Zealand and United Kingdom. Mark Hannibal's co-authors include Jeffrey W. Innis, Catherine E. Keegan, Bernd Wollnik, Mary Beth Dinulos, Simeon A. Boyadjiev, Ethylin Wang Jabs, Otto Daniëls, Robert E. Shapiro, William A. Paznekas and David M. Markovitz and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and PLoS ONE.

In The Last Decade

Mark Hannibal

46 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mark Hannibal United States 22 960 556 236 188 159 48 1.7k
Jean Michel Heard France 28 1.1k 1.2× 860 1.5× 257 1.1× 116 0.6× 297 1.9× 43 2.1k
Éric Bieth France 24 1.1k 1.1× 690 1.2× 56 0.2× 212 1.1× 104 0.7× 72 2.1k
Tomoaki Hishida Japan 23 1.5k 1.5× 210 0.4× 97 0.4× 134 0.7× 78 0.5× 33 1.9k
Margret L. Casal United States 25 833 0.9× 716 1.3× 93 0.4× 120 0.6× 53 0.3× 85 2.0k
Sabine Guth Switzerland 16 1.7k 1.7× 431 0.8× 121 0.5× 69 0.4× 53 0.3× 23 2.2k
Christine Brisson France 23 730 0.8× 200 0.4× 191 0.8× 111 0.6× 33 0.2× 42 1.8k
P. C. P. Ferreira Brazil 7 843 0.9× 208 0.4× 159 0.7× 53 0.3× 170 1.1× 15 1.4k
Mark E. O’Malley United States 23 715 0.7× 800 1.4× 373 1.6× 86 0.5× 85 0.5× 31 1.8k
Colleen S. Stein United States 20 1.3k 1.4× 1.0k 1.9× 231 1.0× 75 0.4× 39 0.2× 35 2.3k
Joan Overhauser United States 31 1.9k 2.0× 1.9k 3.4× 180 0.8× 178 0.9× 65 0.4× 86 3.4k

Countries citing papers authored by Mark Hannibal

Since Specialization
Citations

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

Fields of papers citing papers by Mark Hannibal

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mark Hannibal

This figure shows the co-authorship network connecting the top 25 collaborators of Mark Hannibal. A scholar is included among the top collaborators of Mark Hannibal 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 Mark Hannibal. Mark Hannibal 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.
Ney, Gina M., et al.. (2023). Absolute neutrophil count nadir in healthy pediatric patients with the Duffy-null phenotype. Blood Advances. 7(15). 4182–4185. 2 indexed citations
2.
Walkovich, Kelly, Nadine Saad, Mark Hannibal, et al.. (2022). SOCS1 Haploinsufficiency Presenting as Severe Enthesitis, Bone Marrow Hypocellularity, and Refractory Thrombocytopenia in a Pediatric Patient with Subsequent Response to JAK Inhibition. Journal of Clinical Immunology. 42(8). 1766–1777. 15 indexed citations
3.
Powell, Allison R., et al.. (2021). Symptom Prevalence and Genotype-Phenotype Correlations in Patients With TANGO2-Related Metabolic Encephalopathy and Arrhythmias (TRMEA). Pediatric Neurology. 119. 34–39. 16 indexed citations
4.
Beck, David B., Megan T. Cho, Francisca Millan, et al.. (2016). A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. Neurogenetics. 17(3). 173–178. 25 indexed citations
5.
Srivastava, Anshika, Fengyun Su, Xuhong Cao, et al.. (2015). De novodominantASXL3mutations alter H2A deubiquitination and transcription in Bainbridge–Ropers syndrome. Human Molecular Genetics. 25(3). 597–608. 49 indexed citations
6.
Landsverk, Megan, Douglas C. Weiser, Mark Hannibal, & David Kimelman. (2010). Alternative Splicing of sept9a and sept9b in Zebrafish Produces Multiple mRNA Transcripts Expressed Throughout Development. PLoS ONE. 5(5). e10712–e10712. 11 indexed citations
7.
Kapur, Raj P., Stephen P. Robertson, Mark Hannibal, et al.. (2010). Diffuse Abnormal Layering of Small Intestinal Smooth Muscle is Present in Patients With FLNA Mutations and X-linked Intestinal Pseudo-obstruction. The American Journal of Surgical Pathology. 34(10). 1528–1543. 42 indexed citations
8.
Inamoto, Sakiko, Callie Kwartler, Andrea L. Lafont, et al.. (2010). TGFBR2 mutations alter smooth muscle cell phenotype and predispose to thoracic aortic aneurysms and dissections. Cardiovascular Research. 88(3). 520–529. 97 indexed citations
9.
Collie, Angela M. B., Megan Landsverk, Elizabeth K. Ruzzo, et al.. (2009). Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy. Journal of Medical Genetics. 47(9). 601–607. 35 indexed citations
10.
Hannibal, Mark, et al.. (2009). The Floppy Infant: Evaluation of Hypotonia. Pediatrics in Review. 30(9). e66–e76. 47 indexed citations
11.
Hannibal, Mark, Elizabeth K. Ruzzo, Jillian G. Buchan, et al.. (2009). SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy. Neurology. 72(20). 1755–1759. 40 indexed citations
12.
Landsverk, Megan, Elizabeth K. Ruzzo, Heather C. Mefford, et al.. (2009). Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy. Human Molecular Genetics. 18(7). 1200–1208. 22 indexed citations
13.
Tsuchiya, Karen D., Kent E. Opheim, Mark Hannibal, et al.. (2008). Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization. Molecular Cytogenetics. 1(1). 7–7. 28 indexed citations
14.
Perkins, Jonathan A., Richard M. Tempero, Mark Hannibal, & Scott C. Manning. (2007). Clinical Outcomes in Lymphocytopenic Lymphatic Malformation Patients. Lymphatic Research and Biology. 5(3). 169–174. 21 indexed citations
15.
Paznekas, William A., Simeon A. Boyadjiev, Robert E. Shapiro, et al.. (2003). Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia. The American Journal of Human Genetics. 72(2). 408–418. 487 indexed citations
16.
Hannibal, Mark, et al.. (1999). FVB/N ( H2 q ) mouse is resistant to arthritis induction and exhibits a genomic deletion of T-cell receptor V beta gene segments. Immunogenetics. 49(10). 851–859. 24 indexed citations
17.
Hannibal, Mark, Jon P. Anderson, Stephen R. Lasky, et al.. (1999). T-cell receptor Vbeta deletion and Valpha polymorphism are responsible for the resistance of SWR mouse to arthritis induction. Immunogenetics. 49(9). 764–772. 11 indexed citations
18.
Clark, Nina M., Mark Hannibal, & David M. Markovitz. (1995). The peri-kappa B site mediates human immunodeficiency virus type 2 enhancer activation in monocytes but not in T cells. Journal of Virology. 69(8). 4854–4862. 20 indexed citations
19.
20.
Markovitz, David M., et al.. (1992). Activation of the human immunodeficiency virus type 1 enhancer is not dependent on NFAT-1. Journal of Virology. 66(6). 3961–3965. 30 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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