John Pappas

2.8k citations

54 papers · 885 indexed · h-index 17

Impact in

Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
Otorhinolaryngology top 10%

Papers in ⓘ

Genetics 18
- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 4
Immunology 10
- Immunotherapy and Immune Responses 5
- T-cell and B-cell Immunology 3
- Immune Cell Function and Interaction 3

Co-authors: Charlotte Colp (1 shared paper)Rachel D. Burnside (3 shared papers)C. Papavasiliou (4 shared papers)Inder Gadi (2 shared papers)Vikram Jaswaney (2 shared papers)Peter Papenhausen (2 shared papers)M. Pavlatou (2 shared papers)Stuart Schwartz (2 shared papers)
Journals: International Journal of Radiation Oncology*Biology*Physics (2 papers)Molecular Genetics and Metabolism (2 papers)Cancer (1 paper)European Journal of Human Genetics (1 paper)Nature Communications (1 paper)
Partner nations: United States Greece Canada

In The Last Decade

John Pappas

51 papers receiving 833 citations

Peers

Countries citing papers authored by John Pappas

Since Specialization

Citations

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

Fields of papers citing papers by John Pappas

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 54 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	UPD detection using homozygosity profiling with a SNP genotyping microarray American Journal of Medical Genetics Part A ·Peter Papenhausen, Stuart Schwartz, Hiba Risheg, Elisabeth A. Keitges, Inder Gadi, Rachel D. Burnside, Vikram Jaswaney, John Pappas, Romela Pasion, Kenneth J. Friedman, James Tepperberg	2011	115
2	De novo mutations in KIF1A cause progressive encephalopathy and brain atrophy Annals of Clinical and Translational Neurology ·Sahar Esmaeeli Nieh, Maura R.Z. Madou, Minhajuddin Sirajuddin, Brieana Fregeau, Dianalee McKnight, Katrina W. Lexa, Jonathan B. Strober, Christine G. Spaeth, Barbara Hallinan, Nizar Smaoui, John Pappas, Thomas Andrew Burrow, Marie McDonald, Mariam Latibashvili, Esther Leshinsky‐Silver, Dorit Lev, Luba Blumkin, Ronald D. Vale, A. James Barkovich, Elliott H. Sherr	2015	76
3	Variants of α1-Antitrypsin in Puerto Rican Children With Asthma CHEST Journal ·Charlotte Colp, John Pappas, Donald W. Moran, Jack Liebemuin	1993	60
4	A heat shock protein based polyvalent vaccine targeting HSV-2: CD4+ and CD8+ cellular immunity and protective efficacy Vaccine ·Annie X. Mo, Cristina Musselli, Hong Chen, John Pappas, Kenneth LeClair, Aston Liu, Roman M. Chicz, Alemseged Truneh, Stephen Monks, Daniel L. Levey, Pramod K. Srivastava	2011	38
5	In vivo epigenetic editing of Sema6a promoter reverses transcallosal dysconnectivity caused by C11orf46/Arl14ep risk gene Nature Communications ·Cyril Peter, Atsushi Saito, Yuto Hasegawa, Yuya Tanaka, Mohika Nagpal, Gabriel Pérez‐Lucas, Emily Alway, Sergio Espeso‐Gil, Tariq Fayyad, Chana Ratner, Aslihan Dincer, Achla Gupta, Lakshmi A. Devi, John Pappas, François Lalonde, John A. Butman, Joan C. Han, Schahram Akbarian, Atsushi Kamiya	2019	37
6	Well-differentiated Pancreatic Neuroendocrine Carcinoma in Tuberous Sclerosis—Case Report and Review of the Literature The American Journal of Surgical Pathology ·Nicoleta C. Arva, John Pappas, Teena Bhatla, Elizabeth A. Raetz, Michael Macari, Howard B. Ginsburg, Cristina Hajdu	2011	37
7	A stop codon mutation in COL11A2 induces exon skipping and leads to non‐ocular Stickler syndrome American Journal of Medical Genetics Part A ·Mirka M. Vuoristo, John Pappas, Valerie Jansen, Leena Ala‐Kokko	2004	37
8	Nasopharyngeal cancer in patients under the age of thirty years Cancer ·C. Papavasiliou, M. Pavlatou, John Pappas	1977	37
9	Expansion of phenotype and genotypic data in CRB2-related syndrome European Journal of Human Genetics ·Ryan E. Lamont, Wen‐Hann Tan, A. Micheil Innes, Jillian S. Parboosingh, Dina Schneidman‐Duhovny, Aleksandar Rajkovic, John Pappas, Pablo Altschwager, Stephanie J. DeWard, Anne B. Fulton, Kathryn J. Gray, Max Krall, Lakshmi Mehta, Lance H. Rodan, Devereux N. Saller, Deanna Steele, Deborah R. Stein, Svetlana A. Yatsenko, François P. Bernier, Anne Slavotinek	2016	36
10	Immune responses to human tumors: development of tumor vaccines. PubMed ·Chris D. Platsoucas, John E. Fincke, John Pappas, Weon-Ju Jung, M Heckel, Roland Schwarting, Eleni Magira, Dimitri Monos, Ralph S. Freedman	2003	36
11	Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype American Journal of Medical Genetics Part A ·Rachel D. Burnside, John Pappas, Stephanie Sacharow, Carolyn Applegate, Ada Hamosh, Inder Gadi, Vikram Jaswaney, Elisabeth A. Keitges, Karen Phillips, Venketaswara R. Potluri, Hiba Risheg, Janice Smith, J.H. Tepperberg, Stuart Schwartz, Peter Papenhausen	2013	30
12	Quantitative Systems Pharmacology Modeling of Acid Sphingomyelinase Deficiency and the Enzyme Replacement Therapy Olipudase Alfa Is an Innovative Tool for Linking Pathophysiology and Pharmacology CPT Pharmacometrics & Systems Pharmacology ·Chanchala Kaddi, Bradley Niesner, Rena Baek, Paul Jasper, John Pappas, John Tolsma, Jing Li, Zachary van Rijn, Mengdi Tao, Catherine Ortemann‐Renon, Rachael Easton, Sharon Tan, Ana Cristina Puga, Edward H. Schuchman, Jeffrey S. Barrett, Karim Azer	2018	29
13	Loss‐of‐function variants in NFIA provide further support that NFIA is a critical gene in 1p32‐p31 deletion syndrome: A four patient series American Journal of Medical Genetics Part A ·Anya Revah‐Politi, Mythily Ganapathi, Louise Bier, Megan T. Cho, David B. Goldstein, Parisa Hemati, Alejandro Iglesias, Jane Juusola, John Pappas, Slavé Petrovski, Ashley Wilson, Vimla S. Aggarwal, Kwame Anyane‐Yeboa	2017	28
14	The third component of Xenopus complement: cDNA cloning, structural and functional analysis, and evidence for an alternate C3 transcript European Journal of Immunology ·John D. Lambris, John Pappas, Manolis Mavroidis, Yang Wang, Holly Manzone, Joseph Swager, Louis Du Pasquier, Randi Silibovsky	1995	22
15	De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca ²⁺ regulation Proceedings of the National Academy of Sciences ·Matthew Halvorsen, Laura Gould, Xiaohan Wang, Gariel Grant, Raquel Moya, Rachel Rabin, Michael J. Ackerman, David J. Tester, Peter T. Lin, John Pappas, Matthew T. Maurano, David B. Goldstein, Richard W. Tsien, Orrin Devinsky	2021	21
16	Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and Photophobia The American Journal of Human Genetics ·Lynn M. Boyden, Lihi Atzmony, Claire Hamilton, Jing Zhou, Young Hee Lim, Rong‐Hua Hu, John Pappas, Rachel Rabin, Joseph Ekstien, Yoel Hirsch, Julie Prendiville, Richard P. Lifton, Shawn M. Ferguson, Keith A. Choate	2019	18
17	Treatment of cervical carcinoma by total hysterectomy and postoperative external irradiation International Journal of Radiation OncologyBiologyPhysics ·Constantine Papavasiliou, Demetrios Yiogarakis, John Pappas, Antonios Keramopoulos	1980	18
18	Early presentation of bilateral gonadoblastomas in a Denys-Drash syndrome patient: a cautionary tale for prophylactic gonadectomy Journal of Pediatric Endocrinology and Metabolism ·Payal R. Patel, John Pappas, Nicoleta C. Arva, Bonita Franklin, Preneet Cheema Brar	2013	16
19	The Clinical Course of an Overgrowth Syndrome, From Diagnosis in Infancy Through Adulthood: The Case of Beckwith–Wiedemann Syndrome Current problems in pediatric and adolescent health care ·John Pappas	2015	15
20	Successful pregnancy outcome in Ehlers–Danlos syndrome, vascular type The Journal of Maternal-Fetal & Neonatal Medicine ·Maria Palmquist, John Pappas, Boris M. Petrikovsky, Karin J. Blakemore, Daniel Roshan	2009	14

About John Pappas

John Pappas is a scholar working on Genetics, Immunology, Developmental Biology, Molecular Biology and Oncology, having authored 54 papers that have together received 885 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Immunotherapy and Immune Responses (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), T-cell and B-cell Immunology (3 papers), Immune Cell Function and Interaction (3 papers), Lysosomal Storage Disorders Research (3 papers), DNA Repair Mechanisms (3 papers) and Congenital heart defects research (3 papers). The work is most often cited by research in Genetics (309 citations), Otorhinolaryngology (30 citations), Pediatrics, Perinatology and Child Health (125 citations), Immunology (118 citations) and Cell Biology (81 citations). John Pappas has collaborated with scholars based in United States, Greece and Canada. Frequent co-authors include Charlotte Colp, Rachel D. Burnside, C. Papavasiliou, Inder Gadi, Vikram Jaswaney, Peter Papenhausen, M. Pavlatou, Stuart Schwartz, Hiba Risheg and Elisabeth A. Keitges. Their work appears in journals such as International Journal of Radiation Oncology*Biology*Physics, Molecular Genetics and Metabolism, Cancer, European Journal of Human Genetics and Nature Communications.

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.

Explore authors with similar magnitude of impact