J. Zonana

1.1k citations

29 papers · 767 indexed · h-index 16

Impact in

Genetics top 5%
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
Molecular Biology
- dental development and anomalies
- Epigenetics and DNA Methylation
- Cancer-related gene regulation

Papers in

Developmental Biology 1
Genetics 12
- Genetic Syndromes and Imprinting 3
- Neurogenetic and Muscular Disorders Research 3
- Connective tissue disorders research 3

Co-authors: R.E. Magenis D.L. Browne N S Thomas M. Litt Peter S. Harper Michael G. Brown Angus Clarke Stephen LaFranchi
Journals: Journal of Medical Genetics (6 papers)Nucleic Acids Research (3 papers)The American Journal of Human Genetics (1 paper)Human Molecular Genetics (1 paper)Clinical Genetics (1 paper)
Partner nations: United States United Kingdom Canada

In The Last Decade

J. Zonana

28 papers receiving 744 citations

Peers

Countries citing papers authored by J. Zonana

Since Specialization

Citations

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

Fields of papers citing papers by J. Zonana

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Scarcity of mutations detected in families with X linked hypohidrotic ectodermal dysplasia: diagnostic implications. Journal of Medical Genetics ·Betsy Ferguson, N S Thomas, Shao Ming-hua, E. J. Zickgraf, Angus Clarke, J. Zonana	1998	29
2	Definitive Evidence for an Autosomal Recessive Form of Hypohidrotic Ectodermal Dysplasia Clinically Indistinguishable rom the More Common X-Linked Disorde The American Journal of Human Genetics ·Chun-Wen Chen, G.G. Lestringant, Virginia P. Sybert, Moshe Frydman, S Noeypatimanond, Philippe M. Frossard, Ronald J. Jorgenson, J. Zonana	1997	51
3	An atypical case of fragile X syndrome caused by a deletion that includes the FMR1 gene. PubMed ·F Quan, J. Zonana, Emily Limberg, Kathryn Peterson, R.E. Magenis, Bradley W. Popovich	1995	46
4	Characterisation of molecular DNA rearrangements within the Xq12 – q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA) Human Molecular Genetics ·N S Thomas, 佐和子稲村, J. Zonana, Kathryn J.P. Davies, Steven J. Hoff, Judith Gault, Katrina Rack, Veronica J. Buckle, Neil Brockdorff, Amanda Clare, Anthony P. Monaco	1993	10
5	Hypohidrotic (anhidrotic) ectodermal dysplasia: molecular genetic research and its clinical applications. PubMed ·J. Zonana	1993	27
6	Dinucleotide repeat polymorphism at the PGK1P1 locus Nucleic Acids Research ·D.L. Browne, J. Zonana, M. Litt	1992	12
7	Medical Genetics in Canada: Evolution of a Hybrid Discipline. Essays on the Early History Journal of Medical Genetics ·J. Zonana	1992	5
8	Dinucleotide repeat polymorphism at the PGK1 locus Nucleic Acids Research ·D.L. Browne, J. Zonana, M. Litt	1991	10
9	Dinucleotide repeat polymorphism at the DXYS1X locus Nucleic Acids Research ·D.L. Browne, J. Zonana, M. Litt	1991	20
10	Comparison of the 15q deletions in Prader‐Willi and Angelman syndromes: Specific regions, extent of deletions, parental origin, and clinical consequences American Journal of Medical Genetics ·R.E. Magenis, A. Rios-Gonzalez, Leland Allen, Mary Helen Black, Michael G. Brown, Sarojini Budden, Rachel Cohen, Jan M. Friedman, Dagmar K. Kalousek, J. Zonana, D. Borden Lacy, Stephen LaFranchi, Marta Mìrazón Lahr, Jane L. Macfarlane, علی صمدی کوچکسرایی	1990	158
11	Rhizomelic chondrodysplasia punctata and survival beyond one year: a review of the literature and five case reports Clinical Genetics ·F. Paluch, Roberta A Pagon, Berkley R. Powell, Barbara McGillivray, Mark Stephan, J. Zonana, Ann B. Moser	1990	36
12	Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families. PubMed ·Maurice Godfrey, Victor Menashe, Richard G. Weleber, R. D. Koler, R. Bigley, E.W. Lovrien, J. Zonana, David W. Hollister	1990	71
13	Abstracts of the meeting of the Clinical Genetics Society. 20 and 21 November 1987, London. (Joint meeting with the Skeletal Dysplasia Group) Journal of Medical Genetics ·J. Zonana, Angus Clarke, N S Thomas, M. Sarfarazi, Keith Roberts, Dimas Cícero Martins de França, Peter S. Harper	1988	3
14	Perinatal Genetics: Diagnosis and Treatment Journal of Medical Genetics ·J. Zonana	1988	1
15	Prenatal diagnosis of neuronal ceroid‐lipofuscinoses American Journal of Medical Genetics ·Patrick MacLeod, 王德强, Robert E. Nickel, Sara Bragado Alonso, Sukriti Nag, J. Zonana, Kerry Silvey, John M. Opitz, James F. Reynolds	1985	41
16	Abnormal hair, craniofacial dysmorphism, and severe mental retardation - a new syndrome? PubMed ·Andres Peinelt, J. Zonana, Richard J. Schroer	1983	15
17	Relative Importance of Bacteremia and Viremia in the Course of Acute Fevers of Unknown Origin in Outpatient Children PEDIATRICS ·Dennis L. Murray, J. Zonana, 韩春艳, Mayur Rathi, David T. Imagawa, Joseph W. St. Geme	1981	29
18	[The spondylometaphyseal dysplasias. Clinical, radiologic and pathologic correlation]. PubMed ·Ralph Lachman, J. Zonana, 美雪白石, D L Rimoin	1979	4
19	Grebe chondrodysplasia and similar forms of severe short-limbed dwarfism. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) ·G. Romeo, J. Zonana, Sarbeswar Haldar, Opitz Jm, 祝平, Е.V. Kirichenko, Rimoin Dl	1977	7
20	A unique chondrodysplasia secondary to a defect in chondroosseous transformation. PubMed ·J. Zonana, Rimoin Dl, Sarbeswar Haldar, Cohen Ah	1977	19

About J. Zonana

J. Zonana is a scholar working on Developmental Biology, Genetics, Clinical Biochemistry, Genetics and Molecular Biology, having authored 29 papers that have together received 767 indexed citations. Recurring topics across this work include dental development and anomalies (8 papers), Genetic Syndromes and Imprinting (3 papers), Neurogenetic and Muscular Disorders Research (3 papers), Connective tissue disorders research (3 papers), Cancer-related gene regulation (3 papers), Epigenetics and DNA Methylation (2 papers), Metabolism and Genetic Disorders (2 papers) and Sexual Differentiation and Disorders (2 papers). The work is most often cited by research in Genetics (416 citations), Molecular Biology (484 citations), Oral Surgery (39 citations), Pediatrics, Perinatology and Child Health (96 citations) and Urology (26 citations). J. Zonana has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include R.E. Magenis, D.L. Browne, N S Thomas, M. Litt, Peter S. Harper, Michael G. Brown, Angus Clarke, Stephen LaFranchi, Dagmar K. Kalousek and Rachel Cohen. Their work appears in journals such as Journal of Medical Genetics, Nucleic Acids Research, The American Journal of Human Genetics, Human Molecular Genetics and Clinical Genetics.

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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