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

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 Kirk B. Lane, John A. Phillips et al. profile →
Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis

2007 920 citations Mary Armanios, Julian J.‐L. Chen et al. 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 →

Peers

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

#	Work	Indexed citations
1	Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant 2024 ·American Journal of Medical Genetics Part A ·(unknown), Rory J. Tinker, Yutaka Furuta, Alican Gulsevin, Lisa Bastarache, Rizwan Hamid, Joy D. Cogan, Lynette Rives, (unknown), (unknown), (unknown), John A. Phillips, (unknown)	1
2	A review of multiple diagnostic approaches in the undiagnosed diseases network to identify inherited metabolic diseases 2024 ·Orphanet Journal of Rare Diseases ·Yutaka Furuta, Rory J. Tinker, Rizwan Hamid, Joy D. Cogan, (unknown), Devin Oglesbee, Ralph J. DeBerardinis, John A. Phillips, (unknown)	2
3	The Clinical Spectrum of Mosaic Genetic Disease 2024 ·Genes ·(unknown), Yutaka Furuta, (unknown), John A. Phillips, Rory J. Tinker	1
4	157 Patterns of lung ventilation anomalies in children with cystic fibrosis: case studies from an X-ray velocimetry functional imaging pilot and feasibility study 2024 ·Journal of Cystic Fibrosis ·(unknown), Kristin Carson‐Chahhoud, (unknown), (unknown), John A. Phillips, Nina Eikelis, Andrew Tai, (unknown), (unknown)	1
5	Efficacy and safety of a synthetic biotic for treatment of phenylketonuria: a phase 2 clinical trial 2023 ·Nature Metabolism ·Jerry Vockley, Neal Sondheimer, Marja Puurunen, George A. Díaz, (unknown), Dorothy K. Grange, Cary O. Harding, Hope Northrup, John A. Phillips, (unknown), Janet A. Thomas, Roberto T. Zori, William S. Denney, Sharon L. Ernst, (unknown), (unknown), Caroline Kurtz, Aoife M. Brennan	41
6	Probable digenic inheritance of Diamond–Blackfan anemia 2023 ·American Journal of Medical Genetics Part A ·Yutaka Furuta, Rory J. Tinker, Alican Gulsevin, (unknown), Rizwan Hamid, Joy D. Cogan, Lynette Rives, Qi Liu, Hua‐Chang Chen, Karen M. Joos, John A. Phillips, (unknown)	3
7	A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay 2022 ·Human Mutation ·Hongzheng Dai, Wenmiao Zhu, Bo Yuan, Sophie Nicole, Kelly Schoch, Yong‐hui Jiang, John A. Phillips, Melissa S. Jones, Pengfei Liu, David R. Murdock, Lindsay C. Burrage, Brendan Lee, Jill A. Rosenfeld, Rui Xiao, (unknown)	3
8	Familial Autonomic Ganglionopathy Caused by Rare CHRNA3 Genetic Variants 2021 ·Neurology ·Cyndya A. Shibao, Karen M. Joos, John A. Phillips, Joy D. Cogan, John H. Newman, Rizwan Hamid, Jens Meiler, John A. Capra, Jonathan H. Sheehan, Francesco Vetrini, Yaping Yang, Bonnie K. Black, André Diedrich, (unknown), Italo Biaggioni	8
9	Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer–Rokitansky–Küster–Hauser Syndrome 2021 ·Human Genetics ·Sasha Mikhael, (unknown), (unknown), Lynn P. Chorich, (unknown), Amy C. Lossie, Hyung‐Goo Kim, James Knight, Hugh S. Taylor, Souhrid Mukherjee, John A. Capra, John A. Phillips, Michael J. Friez, Lawrence C. Layman	19
10	Safety and pharmacodynamics of an engineered E. coli Nissle for the treatment of phenylketonuria: a first-in-human phase 1/2a study 2021 ·Nature Metabolism ·Marja Puurunen, Jerry Vockley, (unknown), Stephanie Sacharow, John A. Phillips, William S. Denney, Benjamin D. Goodlett, David A. Wagner, Larry Blankstein, Mary Joan Castillo, Mark R. Charbonneau, Vincent M. Isabella, (unknown), Richard J. Riese, Caroline Kurtz, Aoife M. Brennan	105
11	Development and Progression of Radiologic Abnormalities in Individuals at Risk for Familial Interstitial Lung Disease 2020 ·American Journal of Respiratory and Critical Care Medicine ·Margaret L. Salisbury, J.C. Hewlett, Guixiao Ding, Cheryl Markin, (unknown), Wendi R. Mason, Adam Guttentag, John A. Phillips, Joy D. Cogan, Sara Reiss, Daphne B. Mitchell, Pingsheng Wu, Lisa R. Young, Lisa Lancaster, James E. Loyd, Stephen M. Humphries, David A. Lynch, Jonathan A. Kropski, Timothy S. Blackwell	50
12	Whole Exome Sequencing to Identify a Novel Gene (Caveolin-1) Associated With Human Pulmonary Arterial Hypertension 2012 ·Circulation Cardiovascular Genetics ·Eric D. Austin, Lijiang Ma, Charles A. LeDuc, Erika B. Rosenzweig, Alain Borczuk, John A. Phillips, Teresa Palomero, Pavel Sumazin, Hyunjae R. Kim, Megha Talati, James West, James E. Loyd, Wendy K. Chung	267
13	Short telomeres are a risk factor for idiopathic pulmonary fibrosis breakdown → 2008 ·Proceedings of the National Academy of Sciences ·Jonathan K. Alder, Julian J.‐L. Chen, Lisa Lancaster, Sonye K. Danoff, (unknown), Joy D. Cogan, Irma Vulto, Mingyi Xie, Xiaodong Qi, Rubin M. Tuder, John A. Phillips, Peter M. Lansdorp, James E. Loyd, Mary Armanios	553
14	Clinical and Pathologic Features of Familial Interstitial Pneumonia 2005 ·American Journal of Respiratory and Critical Care Medicine ·Mark P. Steele, Marcy C. Speer, James E. Loyd, Kevin M. Brown, (unknown), Susan H. Slifer, Lauranell H. Burch, Momen M. Wahidi, John A. Phillips, Thomas A. Sporn, H. Page McAdams, Marvin I. Schwarz, David A. Schwartz	265
15	High Allelic Heterogeneity Between Afro-Brazilians and Euro-Brazilians Impacts Cystic Fibrosis Genetic Testing 2003 ·Genetic Testing ·Salmo Raskin, (unknown), Francisco J.C. Reis, Nelson Augusto Rosário Filho, (unknown), (unknown), John A. Phillips, (unknown), Ruth A. Heim, Elaine A. Sugarman, Christian Probst, Fábio R. Faucz, L. Culpi	19
16	Pulmonary Veno-occlusive Disease Caused by an Inherited Mutation in Bone Morphogenetic Protein Receptor II 2003 ·American Journal of Respiratory and Critical Care Medicine ·James Runo, Cindy L. Vnencak‐Jones, Melissa Prince, James E. Loyd, Lisa Wheeler, Ivan M. Robbins, Kirk B. Lane, John H. Newman, Joyce Johnson, William C. Nichols, John A. Phillips	95
17	Lack of interest by nonpregnant couples in population-based cystic fibrosis carrier screening. 1996 ·PubMed ·Ellen Wright Clayton, Vickie Hannig, Jean P. Pfotenhauer, (unknown), Preston W. Campbell, John A. Phillips	65
18	Cervicomedullary compression in young patients with achondroplasia: Value of comprehensive neurologic and respiratory evaluation 1987 ·The Journal of Pediatrics ·Cheryl S. Reid, Reed E. Pyeritz, Steven E. Kopits, Bernard L. Maria, Henry E. Wang, Robert W. McPherson, Orest Hurko, John A. Phillips, Arthur E. Rosenbaum	108
19	Prenatal diagnosis of lethal perinatal osteogenesis imperfecta (OI Type II) 1982 ·The Journal of Pediatrics ·(unknown), John A. Phillips, Peter H. Byers, (unknown), Karen A. Holbrook, L. Stefan Levin, John P. Dorst, Gregory S. Barsh, Karen E. Peterson, Phillip J. Goldstein	44
20	Ratios of α‐ to β‐globin RNA sequences in the erythropoietic mouse spleen 1979 ·FEBS Letters ·John A. Phillips, (unknown), (unknown), Haig H. Kazazian	1

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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