Mark Hannibal

5.3k citations
48 papers · 1.7k · h-index 22

Impact in

  • Virology top 5%
    • HIV Research and Treatment
  • Genetics top 5%
    • Genomics and Rare Diseases
    • Yersinia bacterium, plague, ectoparasites research
    • Genomic variations and chromosomal abnormalities

Papers in

Co-authors
Jeffrey W. Innis (4 shared papers)Catherine E. Keegan (3 shared papers)William A. Paznekas (1 shared paper)Mary Beth Dinulos (1 shared paper)Ethylin Wang Jabs (1 shared paper)Bernd Wollnik (1 shared paper)Simeon A. Boyadjiev (1 shared paper)Robert E. Shapiro (1 shared paper)
Journals
Blood (4 papers)Journal of Virology (4 papers)Pediatric Research (2 papers)Human Molecular Genetics (2 papers)Immunogenetics (2 papers)
Partner nations
United StatesBelgiumUnited Kingdom

In The Last Decade

Mark Hannibal

46 papers receiving 1.7k citations

Peers

Mark Hannibal
Comparison fields: 5 of 89
  • Virology 159
  • Genetics 503
  • Molecular Biology 903
  • Developmental Biology 26
  • Immunology 222
Replace P. C. P. Ferreira with:
P. C. P. Ferreira Brazil
Joan Overhauser United States
Landian Hu China
A. Ahmed‐Ansari United States
Emilie H. Mules United States
Emily C. Walsh United States
Barbara J. Tennent United States
Sarah T. South United States
Benjamin Yu United States
Erik C. Thorland United States
Mark Hannibal relative to P. C. P. Ferreira Brazil P. C. P. Ferreira's profile →
Citations per field
00.5×2×4×6×7.5×
P. C. P. Ferreira · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Mark Hannibal, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Mark Hannibal Line = papers co-authored together Mark Hannibal links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Connexin 43 (GJA1) Mutations Cause the Pleiotropic Phenotype of Oculodentodigital Dysplasia
The American Journal of Human Genetics ·William A. Paznekas, Simeon A. Boyadjiev, Robert E. Shapiro, Otto Daniëls, Bernd Wollnik, Catherine E. Keegan, Jeffrey W. Innis, Mary Beth Dinulos, Cathy Christian, Mark Hannibal, Ethylin Wang Jabs
2003488
2
Phenotypic spectrum and management issues in Kabuki syndrome
The Journal of Pediatrics ·Hiroshi Kawame, Mark Hannibal, Louanne Hudgins, Roberta A Pagon
1999124
3
TBX5 Genetic Testing Validates Strict Clinical Criteria for Holt-Oram Syndrome
Pediatric Research ·Deborah A. McDermott, Michael Bressan, Jié He, Joseph S. Lee, Salim Aftimos, Martina Brueckner, (unknown), Gail E. Graham, Mark Hannibal, Jeffrey W. Innis, Mary Ella Pierpont, Annick Raas‐Rothschild, Alan Shanske, Wendy E. Smith, Robert H. Spencer, Martin G. St. John-Sutton, Lionel Van Maldergem, Darrel Waggoner, Matthew P. Weber, Craig T. Basson
2005104
4
TGFBR2 mutations alter smooth muscle cell phenotype and predispose to thoracic aortic aneurysms and dissections
Cardiovascular Research ·Sakiko Inamoto, Callie Kwartler, Andrea L. Lafont, Yao Liang, Van Tran Fadulu, Senthil Duraisamy, Marcia Willing, Anthony L. Estrera, Hazim J. Safi, Mark Hannibal, John C. Carey, John E. Wiktorowicz, Filemon K. Tan, Xin‐Hua Feng, Hariyadarshi Pannu, Dianna M. Milewicz
201098
5
Differential regulation of human immunodeficiency viruses (HIVs): a specific regulatory element in HIV-2 responds to stimulation of the T-cell antigen receptor.
Proceedings of the National Academy of Sciences ·David M. Markovitz, Mark Hannibal, Víctor Pérez, Charles J. Gauntt, T M Folks, Gary J. Nabel
199056
6
De novodominantASXL3mutations alter H2A deubiquitination and transcription in Bainbridge–Ropers syndrome
Human Molecular Genetics ·Anshika Srivastava, K.C. Ritesh, Yao-Chang Tsan, Rosy Liao, Fengyun Su, Xuhong Cao, Mark Hannibal, Catherine E. Keegan, Arul M. Chinnaiyan, Donna M. Martin, Stephanie Bielas
201552
7
Molecular consequences of dominant Bethlem myopathy collagen VI mutations
Annals of Neurology ·Naomi L. Baker, Matthias Mörgelin, Rishika A. Pace, Rachel A. Peat, Naomi E. Adams, R. J. McKinlay Gardner, Lewis P. Rowland, Geoffrey Miller, Peter De Jonghe, Berten Ceulemans, Mark Hannibal, Matthew Edwards, Elizabeth M. Thompson, Richard D. Jacobson, Rosaline C. M. Quinlivan, Salim Aftimos, Andrew J. Kornberg, Kathryn N. North, John F. Bateman, Shireen R. Lamandé
200750
8
Activation of the human immunodeficiency virus type 2 enhancer is dependent on purine box and kappa B regulatory elements
Journal of Virology ·David M. Markovitz, Michael J. Smith, J M Hilfinger, Mark Hannibal, B Petryniak, Gary J. Nabel
199250
9
The Floppy Infant: Evaluation of Hypotonia
Pediatrics in Review ·Dawn E. Peredo, Mark Hannibal
200947
10
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 ·Raj P. Kapur, Stephen P. Robertson, Mark Hannibal, Laura S. Finn, Timothy Morgan, Margriet van Kogelenberg, David J. Loren
201043
11
SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy
Neurology ·Mark Hannibal, Elizabeth K. Ruzzo, Lauren Miller, Benjamin G Betz, Jillian G. Buchan, Dana Knutzen, K. Barnett, Megan Landsverk, Alexis Brice, Éric Leguern, H. Melanie Bedford, Bradford B. Worrall, S. Lovitt, Stanley H. Appel, E. Andermann, Thomas D. Bird, P. F. Chance
200940
12
Differential activation of human immunodeficiency virus type 1 and 2 transcription by specific T-cell activation signals
Journal of Virology ·Mark Hannibal, David M. Markovitz, Nina M. Clark, Gary J. Nabel
199339
13
Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy
Journal of Medical Genetics ·Angela M. B. Collie, Megan Landsverk, Elizabeth K. Ruzzo, Heather C. Mefford, Karen Buysse, J. R. Adkins, Dana Knutzen, K. Barnett, Robert H. Brown, G. Parry, Sabrina W. Yum, David Simpson, Richard K. Olney, Patrick F. Chinnery, Evan E. Eichler, P. F. Chance, Mark Hannibal
200936
14
Activation of the human immunodeficiency virus type 1 enhancer is not dependent on NFAT-1
Journal of Virology ·David M. Markovitz, Mark Hannibal, Michael J. Smith, R Cossman, Gary J. Nabel
199230
15
Unexpected structural complexity of supernumerary marker chromosomes characterized by microarray comparative genomic hybridization
Molecular Cytogenetics ·Karen D. Tsuchiya, Kent E. Opheim, Mark Hannibal, Anne Hing, Ian A. Glass, Michael L. Raff, Thomas H. Norwood, Beth A. Torchia
200828
16
Genotype–phenotype analysis of 523 patients by genetics evaluation and clinical exome sequencing
Pediatric Research ·Mark N. Ziats, Ayesha Ahmad, John Bernat, Rachel S. Fisher, Megan R. Glassford, Mark Hannibal, Joseph E. Jacher, Natasha E. Weiser, Catherine E. Keegan, Kristen Lee, Tessa Marzulla, Bridget O’Connor, Shane C. Quinonez, Lauren Seemann, Lauren Turner, Stephanie Bielas, Nicholas Harris, Jacob D. Ogle, Jeffrey W. Innis, Donna M. Martin
201927
17
Lymphocytopenia in Children With Lymphatic Malformation
Archives of Otolaryngology - Head and Neck Surgery ·Richard M. Tempero, Mark Hannibal, Laura S. Finn, Scott C. Manning, Michael L. Cunningham, Jonathan A. Perkins
200626
18
A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects
Neurogenetics ·David B. Beck, Megan T. Cho, Francisca Millan, Carin Yates, Mark Hannibal, Bridget O’Connor, Marwan Shinawi, Anne M. Connolly, Darrel Waggoner, Sara Halbach, Brad Angle, Victoria R. Sanders, Yufeng Shen, Kyle Retterer, Amber Begtrup, Renkui Bai, Wendy K. Chung
201626
19
The Floppy Infant
Pediatrics in Review ·Dawn E. Peredo, Mark Hannibal
200926
20
FVB/N ( H2 q ) mouse is resistant to arthritis induction and exhibits a genomic deletion of T-cell receptor V beta gene segments
Immunogenetics ·G E Osman, Mark Hannibal, Jon P. Anderson, Stephen R. Lasky, Warren Ladiges, Leroy Hood
199924

About Mark Hannibal

Mark Hannibal is a scholar working on Genetics, Molecular Biology, Immunology, Virology and Surgery, having authored 48 papers that have together received 1.7k indexed citations. Recurring topics across this work include Immune Cell Function and Interaction (6 papers), HIV Research and Treatment (6 papers), T-cell and B-cell Immunology (5 papers), Epigenetics and DNA Methylation (4 papers), Genomics and Rare Diseases (4 papers), RNA modifications and cancer (4 papers), Platelet Disorders and Treatments (3 papers) and Immunodeficiency and Autoimmune Disorders (3 papers). The work is most often cited by research in Virology (159 citations), Genetics (503 citations), Molecular Biology (903 citations), Developmental Biology (26 citations) and Immunology (222 citations). Mark Hannibal has collaborated with scholars based in United States, Belgium and United Kingdom. Frequent co-authors include Jeffrey W. Innis, Catherine E. Keegan, William A. Paznekas, Mary Beth Dinulos, Ethylin Wang Jabs, Bernd Wollnik, Simeon A. Boyadjiev, Robert E. Shapiro, Otto Daniëls and David M. Markovitz. Their work appears in journals such as Blood, Journal of Virology, Pediatric Research, Human Molecular Genetics and Immunogenetics.

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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