Jonathan Zonana

6.6k citations

44 papers · 4.1k indexed · 2 hit papers · h-index 22

Impact in

Oral Surgery top 1%
- Oral and Maxillofacial Pathology
Genetics top 2%
- Congenital Ear and Nasal Anomalies

Papers in

Genetics 14
Cancer Research 7
- NF-κB Signaling Pathways 7

Co-authors: Betsy Ferguson Roberta A Pagon John M. Graham Siu‐Li Yong Denis J. Headon Paul A. Overbeek Lynda C. Schneider David L. Rimoin
Journals: The Journal of Pediatrics (6 papers)Nature Genetics (3 papers)Journal of Clinical Investigation (3 papers)Journal of Investigative Dermatology (2 papers)Genetics in Medicine (2 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

Jonathan Zonana

44 papers receiving 3.9k citations

Hit Papers

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X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein 1996 · 557 citations

Peers

Countries citing papers authored by Jonathan Zonana

Since Specialization

Citations

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

Fields of papers citing papers by Jonathan Zonana

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Jonathan Zonana, 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 Jonathan Zonana Line = papers co-authored together Jonathan Zonana links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Congenital Extrarenal Malignant Rhabdoid Tumor in an Infant With Distal 22q11.2 Deletion Syndrome American Journal of Dermatopathology ·XIA Peng 1, 2, ZHOU Yanguo 1, LIU Kai 1, 3, CHEN Yunmin 1, Clifton R. White, Veselina Korcheva, Florence Rodhain, C. M. T. van de Sande-Rijkers, Jonathan Zonana, Stephen Moore, Alfons Krol, Atiya Mansoor	2012	8
2	Genotype–phenotype analysis of TCF4 mutations causing Pitt-Hopkins syndrome shows increased seizure activity with missense mutations Genetics in Medicine ·Jill A. Rosenfeld, Kathleen A. Leppig, Blake C. Ballif, Heidi Thiese, Christine Erdie-Lalena, Chandana Sandireddy, RitaBell, J. Edward Spence, Anne M. Bandholz, Urvashi Surti, Jonathan Zonana, Kory Keller, Wendy S. Meschino, Bassem A. Bejjani, Beth S. Torchia, Lisa G. Shaffer	2009	55
3	Deficient natural killer cell cytotoxicity in patients with IKK-γ/NEMO mutations Journal of Clinical Investigation ·Jordan S. Orange, Scott R. Brodeur, Ashish Jain, Francisco A. Bonilla, Lynda C. Schneider, R Kretschmer, Samuel Nurko, Wendy Rasmussen, Julia R. Köhler, Stephen E. Gellis, Betsy Ferguson, Jack L. Strominger, Jonathan Zonana, Narayanaswamy Ramesh, Zuhair K. Ballas, Raif S. Geha	2002	4
4	Deficient natural killer cell cytotoxicity in patients with IKK-γ/NEMO mutations Journal of Clinical Investigation ·Jordan S. Orange, Scott R. Brodeur, Ashish Jain, Francisco A. Bonilla, Lynda C. Schneider, R Kretschmer, Samuel Nurko, Wendy Rasmussen, Julia R. Köhler, Stephen E. Gellis, Betsy Ferguson, Jack L. Strominger, Jonathan Zonana, Narayanaswamy Ramesh, Zuhair K. Ballas, Raif S. Geha	2002	137
5	Deficient natural killer cell cytotoxicity in patients with IKK-γ/NEMO mutations Journal of Clinical Investigation ·Jordan S. Orange, Scott R. Brodeur, Ashish Jain, Francisco A. Bonilla, Lynda C. Schneider, R Kretschmer, Samuel Nurko, Wendy Rasmussen, Julia R. Köhler, Stephen E. Gellis, Betsy Ferguson, Jack L. Strominger, Jonathan Zonana, Narayanaswamy Ramesh, Zuhair K. Ballas, Raif S. Geha	2002	157
6	Gene defect in ectodermal dysplasia implicates a death domain adapter in development Nature ·Denis J. Headon, Sharon L. Truesdell, Betsy Ferguson, Abigail S. Tucker, Monica J. Justice, Paul T. Sharpe, Jonathan Zonana, Paul A. Overbeek	2001	287
7	Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia Nature Genetics ·Wenni Febriana E. Sueni, Betsy Ferguson, Denis J. Headon, Tiago V. Barra, Paul A. Overbeek, Jonathan Zonana	1999	305
8	Confirmation of Linkage of Clouston Syndrome (Hidrotic Ectodermal Dysplasia) to 13q11-q12.1 with Evidence for Multiple Independent Mutations Journal of Investigative Dermatology ·Todd D. Taylor, Susan J. Hayflick, M. Litt, Jonathan Zonana, Wendy McKinnon, Alan E. Guttmacher, Alain Hovnanian	1998	14
9	Identification of a New Splice Form of the EDA1 Gene Permits Detection of Nearly All X-Linked Hypohidrotic Ectodermal Dysplasia Mutations The American Journal of Human Genetics ·Wenni Febriana E. Sueni, Jonathan Zonana, Betsy Ferguson	1998	164
10	X–linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein Nature Genetics ·Juha Kere, Anand Srivastava, Jana Kukeska, Jonathan Zonana, Nick Thomas, Betsy Ferguson, Shao Ming-hua, Sandip G Tarkas, Angus Clarke, Primo Baybayan, Ellson Y. Chen, Sini Ezer, Ulpu Saarialho‐Kere, Albert de la Chapelle, David Schlessinger Hit paper breakdown →	1996	557
11	Craniofacial Conodysplasia Journal of Pediatric Orthopaedics ·Rodney K. Beals, Joseph H. Piatt, Jonathan Zonana	1995	2
12	Velo‐cardio‐facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region American Journal of Medical Genetics ·Robert E. Nickel, De‐Ann M. Pillers, Nahid Yeasmin, R. Ellen Magenis, Deborah A. Driscoll, Beverly S. Emanuel, Jonathan Zonana	1994	41
13	Congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment: A distinct syndrome American Journal of Medical Genetics ·Roger L. Ladda, Jonathan Zonana, Jeanette C. Ramer, Maria J. Mascari, Peter K. Rogan	1993	5
14	Searching for Human Epilepsy Genes: A Progress Report Brain Pathology ·Mark Leppert, William M. McMahon, Thomas G. Quattlebaum, Ingrid Bjerre, Jonathan Zonana, Michael Shevell, Eva Andermann, Elmira Agagulukizi Quliyeva, Gabriel M. Ronen, Mary Connolly, Vernon Anderson	1993	11
15	Deletions and microdeletions of 22q11.2 in velo‐cardio‐facial syndrome American Journal of Medical Genetics ·Deborah A. Driscoll, Nancy B. Spinner, Marcia L. Budarf, Donna M. McDonald‐McGinn, Elaine H. Zackai, Rosalie Goldberg, Robert J. Shprintzen, Howard M. Saal, Jonathan Zonana, Marilyn C. Jones, James T. Mascarello, Beverly S. Emanuel	1992	299
16	Prenatal diagnosis of X‐linked hypohidrotic ectodermal dysplasia by linkage analysis American Journal of Medical Genetics ·Jonathan Zonana, Albert Schinzel, Meena Upadhyaya, N S Thomas, I. Anton‐Lamprecht, Peter S. Harper	1990	14
17	Lymphedema in Noonan syndrome: Clues to pathogenesis and prenatal diagnosis and review of the literature American Journal of Medical Genetics ·David R. Witt, H. Eugene Hoyme, Jonathan Zonana, David Manchester, J. P. Fryns, J. Geoffrey Stevenson, Cynthia J. Curry, Judith G. Hall, John M. Opitz, James F. Reynolds	1987	105
18	Familial porencephaly and congenital hemiplegia The Journal of Pediatrics ·Jonathan Zonana, Bruce T. Adornato, H. Martin Puchner, Kyung-Hwan Song	1986	18
19	Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association The Journal of Pediatrics ·Roberta A Pagon, John M. Graham, Jonathan Zonana, Siu‐Li Yong Hit paper breakdown →	1981	610
20	Macrocephaly with multiple lipomas and hemangiomas The Journal of Pediatrics ·Jonathan Zonana, David L. Rimoin, David C. Davis	1976	64

About Jonathan Zonana

Jonathan Zonana is a scholar working on Genetics, Cancer Research, Cell Biology, Molecular Biology and Urology, having authored 44 papers that have together received 4.1k indexed citations. Recurring topics across this work include dental development and anomalies (10 papers), NF-κB Signaling Pathways (7 papers), Immune Response and Inflammation (5 papers), Wnt/β-catenin signaling in development and cancer (5 papers), Skin and Cellular Biology Research (4 papers), Congenital heart defects research (4 papers), Tracheal and airway disorders (4 papers) and Fibroblast Growth Factor Research (3 papers). The work is most often cited by research in Oral Surgery (447 citations), Genetics (596 citations), Urology (262 citations), Molecular Biology (2.5k citations) and Genetics (937 citations). Jonathan Zonana has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Betsy Ferguson, Roberta A Pagon, John M. Graham, Siu‐Li Yong, Denis J. Headon, Paul A. Overbeek, Lynda C. Schneider, David L. Rimoin, Angus Clarke and Ulpu Saarialho‐Kere. Their work appears in journals such as The Journal of Pediatrics, Nature Genetics, Journal of Clinical Investigation, Journal of Investigative Dermatology and Genetics in Medicine.

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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