Mark Hannibal

5.3k citations

48 papers · 1.7k indexed · h-index 22

Virology top 5%
- HIV Research and Treatment 6
Genetics top 5%
- Connective tissue disorders research 6
- Genomics and Rare Diseases 4
- Genetic Syndromes and Imprinting 3
Molecular Biology top 10%
- RNA modifications and cancer 5
- Epigenetics and DNA Methylation 4
Developmental Biology top 10%
Immunology top 10%
- Immune Cell Function and Interaction 6
- T-cell and B-cell Immunology 5

Co-authors: Jeffrey W. Innis Catherine E. Keegan Robert E. Shapiro Bernd Wollnik Ethylin Wang Jabs Mary Beth Dinulos Otto Daniëls Simeon A. Boyadjiev
Cited by: Virology Genetics Molecular Biology
Journals: Journal of Virology (4 papers)Blood (4 papers)Human Molecular Genetics (2 papers)
Partner nations: United States Belgium New Zealand

In The Last Decade

Mark Hannibal

46 papers receiving 1.6k citations

Peers

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

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

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20 of 20 papers shown

#	Work
1	Absolute neutrophil count nadir in healthy pediatric patients with the Duffy-null phenotype Blood Advances ·Jian Fu,天野政史,Gina M. Ney,Armin Weschpfennig,Mark Hannibal,Kelly Walkovich	2023	2
2	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 ·Armin Weschpfennig,Kelly Walkovich,憲一郎塚本,Nadine Saad,Mark Hannibal,Matthew L. Basiaga,Kelly K. Horst,HY Zheng,Liang Chen,Correcher,Yan Du,David Frame,Qing Qian-zhi,강효정,Noah A. Brown,Pui Y. Lee	2022	15
3	Kagami–Ogata syndrome in a patient with 46,XX,t(2;14)(q11.2;q32.2)mat disrupting MEG3 Journal of Human Genetics ·Hua-nian Zhang,Yohei Masunaga,Mark Hannibal,M. V. Gapanovich,Maki Fukami,Fumiko Kato,Hirotomo Saitsu,Masayo Kagami,Tsutomu Ogata	2020	1
4	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,Loredana Sasso,Mark Hannibal,Valdemar Marques,Natasha E. Weiser,Catherine E. Keegan,Kristen Lee,Tessa Marzulla,Bridget O’Connor,Shane C. Quinonez,邵琳,Zhengxia Gao,Stephanie Bielas,Nicholas Harris,Abdou SENE,Jeffrey W. Innis,Donna M. Martin	2019	25
5	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,Erika Susana Vivanco Gonzaga,Mark Hannibal,Bridget O’Connor,Marwan Shinawi,Anne M. Connolly,Darrel Waggoner,Sara Halbach,Brad Angle,Tabom Tatak,Yufeng Shen,Kyle Retterer,Amber Begtrup,Renkui Bai,Wendy K. Chung	2016	25
6	De novodominantASXL3mutations alter H2A deubiquitination and transcription in Bainbridge–Ropers syndrome Human Molecular Genetics ·Anshika Srivastava,Mutsuaki Komada,Aquiles Rocha Lira Bezerra,Poorna Chander Kokkula,Fengyun Su,Xuhong Cao,Mark Hannibal,Catherine E. Keegan,Arul M. Chinnaiyan,Donna M. Martin,Stephanie Bielas	2015	49
7	Alternative Splicing of sept9a and sept9b in Zebrafish Produces Multiple mRNA Transcripts Expressed Throughout Development PLoS ONE ·Megan Landsverk,Douglas C. Weiser,Mark Hannibal,David Kimelman	2010	11
8	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	2010	42
9	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,O. Fanar,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	2010	97
10	The Floppy Infant: Evaluation of Hypotonia Pediatrics in Review ·Kevin Sebastian Pesantez Calle,Mark Hannibal	2009	47
11	Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy Human Molecular Genetics ·Megan Landsverk,Elizabeth K. Ruzzo,Heather C. Mefford,Karen Buysse,Jillian G. Buchan,Evan E. Eichler,Elizabeth M. Petty,Esther A. Peterson,Dana Knutzen,J. Hascoet,Martin R. Farlow,Yu Joo Kwon,G. Parry,Dianna Quan,Kathy Gardner,Ismailjani Shaik,Zachary Simmons,Thomas D. Bird,Phillip F. Chance,Mark Hannibal	2009	22
12	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,V.Yu. Novototski-Vlasov,Dana Knutzen,J. Hascoet,Robert H. Brown,G. Parry,Sabrina W. Yum,David Simpson,Richard K. Olney,Patrick F. Chinnery,Evan E. Eichler,P. F. Chance,Mark Hannibal	2009	35
13	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,Inês Maria Benedita Silveira,Thomas H. Norwood,Beth A. Torchia	2008	28
14	Clinical Outcomes in Lymphocytopenic Lymphatic Malformation Patients Lymphatic Research and Biology ·Jonathan A. Perkins,Richard M. Tempero,Mark Hannibal,Scott C. Manning	2007	21
15	Aortic Root Dilatation is a Rare Complication of Noonan Syndrome Pediatric Cardiology ·A Dyanaa,Mark Lewin,Mark Hannibal,Ian A. Glass	2006	16
16	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	2006	26
17	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,Esmeralda Blouin,Mark Hannibal,Ethylin Wang Jabs	2003	487
18	FVB/N ( H2 q ) mouse is resistant to arthritis induction and exhibits a genomic deletion of T-cell receptor V beta gene segments Immunogenetics ·B. Nagorna-Stasiak,Mark Hannibal,Jon P. Anderson,Stephen R. Lasky,Warren Ladiges,Leroy Hood	1999	24
19	Phenotypic spectrum and management issues in Kabuki syndrome The Journal of Pediatrics ·Hiroshi Kawame,Mark Hannibal,Louanne Hudgins,Roberta A Pagon	1999	123
20	T-cell receptor Vbeta deletion and Valpha polymorphism are responsible for the resistance of SWR mouse to arthritis induction Immunogenetics ·B. Nagorna-Stasiak,Mark Hannibal,Jon P. Anderson,Russell O. Gardner,Stephen R. Lasky,H. Denny Liggitt,Warren Ladiges,Leroy Hood	1999	11

About Mark Hannibal

Mark Hannibal is a scholar working on Virology, Genetics, Immunology, Developmental Biology and Genetics, having authored 48 papers that have together received 1.7k indexed citations. Recurring topics across this work include Connective tissue disorders research (6 papers), HIV Research and Treatment (6 papers), Immune Cell Function and Interaction (6 papers), RNA modifications and cancer (5 papers), T-cell and B-cell Immunology (5 papers), Genomics and Rare Diseases (4 papers), Epigenetics and DNA Methylation (4 papers) and Genetic Syndromes and Imprinting (3 papers). The work is most often cited by research in Virology (159 citations), Genetics (556 citations), Molecular Biology (960 citations), Developmental Biology (27 citations) and Immunology (236 citations). Mark Hannibal has collaborated with scholars based in United States, Belgium and New Zealand. Frequent co-authors include Jeffrey W. Innis, Catherine E. Keegan, Robert E. Shapiro, Bernd Wollnik, Ethylin Wang Jabs, Mary Beth Dinulos, Otto Daniëls, Simeon A. Boyadjiev, William A. Paznekas and David M. Markovitz. Their work appears in journals such as Journal of Virology, Blood, Human Molecular Genetics, Immunogenetics and Pediatric Research.

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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