John A. Phillips

22.0k total citations · 3 hit papers
265 papers, 13.3k citations indexed

About

John A. Phillips is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, John A. Phillips has authored 265 papers receiving a total of 13.3k indexed citations (citations by other indexed papers that have themselves been cited), including 85 papers in Molecular Biology, 78 papers in Genetics and 68 papers in Pulmonary and Respiratory Medicine. Recurrent topics in John A. Phillips's work include Growth Hormone and Insulin-like Growth Factors (52 papers), Pulmonary Hypertension Research and Treatments (30 papers) and Genetics and Neurodevelopmental Disorders (20 papers). John A. Phillips is often cited by papers focused on Growth Hormone and Insulin-like Growth Factors (52 papers), Pulmonary Hypertension Research and Treatments (30 papers) and Genetics and Neurodevelopmental Disorders (20 papers). John A. Phillips collaborates with scholars based in United States, United Kingdom and Germany. John A. Phillips's co-authors include James E. Loyd, Joy D. Cogan, Kirk B. Lane, John H. Newman, William C. Nichols, Richard C. Trembath, Rajiv D. Machado, Michael W. Pauciulo, Lisa Wheeler and Jennifer R. Thomson and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

John A. Phillips

259 papers receiving 12.9k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension

2000 1.1k citations John A. Phillips, James E. Loyd et al. profile →
Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis

2007 920 citations Mary Armanios, Julian J.‐L. Chen et al. New England Journal of Medicine profile →
Short telomeres are a risk factor for idiopathic pulmonary fibrosis

2008 553 citations Jonathan K. Alder, Julian J.‐L. Chen et al. Proceedings of the National Academy of Sciences profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
John A. Phillips	5.9k	4.0k	2.5k	2.0k	2.0k	265	13.3k
Richard C. Trembath	5.8k 1.0×	6.3k 1.6×	2.7k 1.1×	1.7k 0.8×	477 0.2×	210	17.3k
Peter Mündel	1.1k 0.2×	8.3k 2.1×	3.2k 1.3×	2.0k 1.0×	744 0.4×	158	20.0k
Martin Farrall	833 0.1×	3.1k 0.8×	3.2k 1.3×	1.7k 0.9×	1.6k 0.8×	123	10.2k
Thomas Quertermous	1.3k 0.2×	6.9k 1.8×	2.2k 0.9×	2.8k 1.4×	1.6k 0.8×	303	17.2k
Mark Lathrop	1.1k 0.2×	5.8k 1.5×	3.7k 1.5×	3.2k 1.6×	827 0.4×	207	14.0k
Cheryl R. Greenberg	1.3k 0.2×	6.3k 1.6×	1.8k 0.7×	1.0k 0.5×	1.7k 0.9×	218	10.2k
David P. Witte	1.6k 0.3×	5.9k 1.5×	1.6k 0.6×	2.0k 1.0×	422 0.2×	240	13.3k
Francesco J. DeMayo	3.0k 0.5×	14.7k 3.7×	8.5k 3.4×	1.4k 0.7×	2.0k 1.0×	401	32.3k
Michael Kashgarian	1.6k 0.3×	5.1k 1.3×	750 0.3×	1.1k 0.5×	819 0.4×	265	13.5k
Charles T. Roberts	1.1k 0.2×	8.4k 2.1×	2.6k 1.0×	1.8k 0.9×	8.4k 4.2×	264	16.9k

Countries citing papers authored by John A. Phillips

Since Specialization

Citations

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

Fields of papers citing papers by John A. Phillips

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of John A. Phillips

This figure shows the co-authorship network connecting the top 25 collaborators of John A. Phillips. A scholar is included among the top collaborators of John A. Phillips based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with John A. Phillips. John A. Phillips is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Bastarache, Lisa, Rory J. Tinker, Bryce Schuler, et al.. (2025). Characterizing trends in clinical genetic testing: A single-center analysis of EHR data from 1.8 million patients over two decades. The American Journal of Human Genetics. 112(5). 1029–1038. 2 indexed citations

Tinker, Rory J., Yutaka Furuta, Alican Gulsevin, et al.. (2024). Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant. American Journal of Medical Genetics Part A. 194(7). e63597–e63597. 1 indexed citations

Furuta, Yutaka, Rory J. Tinker, Rizwan Hamid, et al.. (2024). A review of multiple diagnostic approaches in the undiagnosed diseases network to identify inherited metabolic diseases. Orphanet Journal of Rare Diseases. 19(1). 427–427. 2 indexed citations

Carson‐Chahhoud, Kristin, et al.. (2024). 157 Patterns of lung ventilation anomalies in children with cystic fibrosis: case studies from an X-ray velocimetry functional imaging pilot and feasibility study. Journal of Cystic Fibrosis. 23. S88–S88. 1 indexed citations

Vockley, Jerry, Neal Sondheimer, Marja Puurunen, et al.. (2023). Efficacy and safety of a synthetic biotic for treatment of phenylketonuria: a phase 2 clinical trial. Nature Metabolism. 5(10). 1685–1690. 41 indexed citations

Furuta, Yutaka, Rory J. Tinker, Alican Gulsevin, et al.. (2023). Probable digenic inheritance of Diamond–Blackfan anemia. American Journal of Medical Genetics Part A. 194(3). e63454–e63454. 3 indexed citations

Dai, Hongzheng, Wenmiao Zhu, Bo Yuan, et al.. (2022). A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay. Human Mutation. 43(12). 1816–1823. 3 indexed citations

Puurunen, Marja, Jerry Vockley, Stephanie Sacharow, et al.. (2021). Safety and pharmacodynamics of an engineered E. coli Nissle for the treatment of phenylketonuria: a first-in-human phase 1/2a study. Nature Metabolism. 3(8). 1125–1132. 105 indexed citations

Shibao, Cyndya A., Karen M. Joos, John A. Phillips, et al.. (2021). Familial Autonomic Ganglionopathy Caused by Rare CHRNA3 Genetic Variants. Neurology. 97(2). e145–e155. 8 indexed citations

10.

Mikhael, Sasha, Lynn P. Chorich, Amy C. Lossie, et al.. (2021). Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer–Rokitansky–Küster–Hauser Syndrome. Human Genetics. 140(4). 667–680. 19 indexed citations

11.

Salisbury, Margaret L., J.C. Hewlett, Guixiao Ding, et al.. (2020). Development and Progression of Radiologic Abnormalities in Individuals at Risk for Familial Interstitial Lung Disease. American Journal of Respiratory and Critical Care Medicine. 201(10). 1230–1239. 50 indexed citations

12.

Austin, Eric D., Lijiang Ma, Charles A. LeDuc, et al.. (2012). Whole Exome Sequencing to Identify a Novel Gene (Caveolin-1) Associated With Human Pulmonary Arterial Hypertension. Circulation Cardiovascular Genetics. 5(3). 336–343. 267 indexed citations

13.

Alder, Jonathan K., Julian J.‐L. Chen, Lisa Lancaster, et al.. (2008). Short telomeres are a risk factor for idiopathic pulmonary fibrosis. Proceedings of the National Academy of Sciences. 105(35). 13051–13056. 553 indexed citations breakdown →

14.

Armanios, Mary, Julian J.‐L. Chen, Joy D. Cogan, et al.. (2007). Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis. New England Journal of Medicine. 356(13). 1317–1326. 920 indexed citations breakdown →

15.

Steele, Mark P., Marcy C. Speer, James E. Loyd, et al.. (2005). Clinical and Pathologic Features of Familial Interstitial Pneumonia. American Journal of Respiratory and Critical Care Medicine. 172(9). 1146–1152. 265 indexed citations

16.

Raskin, Salmo, Francisco J.C. Reis, Nelson Augusto Rosário Filho, et al.. (2003). High Allelic Heterogeneity Between Afro-Brazilians and Euro-Brazilians Impacts Cystic Fibrosis Genetic Testing. Genetic Testing. 7(3). 213–218. 19 indexed citations

17.

Clayton, Ellen Wright, et al.. (1996). Lack of interest by nonpregnant couples in population-based cystic fibrosis carrier screening.. PubMed. 58(3). 617–27. 65 indexed citations

18.

Reid, Cheryl S., Reed E. Pyeritz, Steven E. Kopits, et al.. (1987). Cervicomedullary compression in young patients with achondroplasia: Value of comprehensive neurologic and respiratory evaluation. The Journal of Pediatrics. 110(4). 522–530. 108 indexed citations

19.

Phillips, John A., Peter H. Byers, Karen A. Holbrook, et al.. (1982). Prenatal diagnosis of lethal perinatal osteogenesis imperfecta (OI Type II). The Journal of Pediatrics. 100(1). 127–133. 44 indexed citations

20.

Phillips, John A., et al.. (1979). Ratios of α‐ to β‐globin RNA sequences in the erythropoietic mouse spleen. FEBS Letters. 97(2). 327–329. 1 indexed citations

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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