Jennifer J. Johnston

6.5k citations

55 papers · 3.1k indexed · 1 hit paper · h-index 25

Molecular Biology top 5%
Genetics top 2%
Pharmacology top 2%
Cardiology and Cardiovascular Medicine top 5%
Epidemiology top 10%

Co-authors: Leslie G. Biesecker Joseph Dinchuk James M. Trzăskos Bruce D. Car Vicki M. Eng Nancy Contel Bruce Jaffee Richard J. Focht
Topics: Genomics and Rare Diseases (12 papers)Hedgehog Signaling Pathway Studies (9 papers)Genetic and Kidney Cyst Diseases (8 papers)
Cited by: Endocrine and Autonomic Systems Genetics Pharmacology
Journals: Nature Journal of Biological ChemistrySHILAP Revista de lepidopterología
Partner nations: United States United Kingdom Canada

In The Last Decade

Jennifer J. Johnston

52 papers receiving 3.0k 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.

Renal abnormalities and an altered inflammatory response in mice lacking cyclooxygenase II

1995 805 citations Jennifer J. Johnston et al. profile →

Peers

Countries citing papers authored by Jennifer J. Johnston

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer J. Johnston

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer J. Johnston

This figure shows the co-authorship network connecting the top 25 collaborators of Jennifer J. Johnston. A scholar is included among the top collaborators of Jennifer J. Johnston 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 Jennifer J. Johnston. Jennifer J. Johnston 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	Clinical and molecular heterogeneity of syndromic hypothalamic hamartoma 2023 ·American Journal of Medical Genetics Part A ·Carsten G. Bönnemann,Kalpathy S. Krishnamoorthy,Jennifer J. Johnston,Mary Lee,Darren Fowler,Leslie G. Biesecker,Lewis B. Holmes	0
2	Genome-wide identification of dominant polyadenylation hexamers for use in variant classification 2023 ·Human Molecular Genetics ·(unknown),Celine Hong,D.N. Cooper,Jennifer J. Johnston,(unknown),Leslie G. Biesecker	1
3	Updated variant curation expert panel criteria and pathogenicity classifications for 251 variants for RYR1 -related malignant hyperthermia susceptibility 2022 ·Human Molecular Genetics ·Jennifer J. Johnston,Robert T. Dirksen,Thierry Girard,Philip M. Hopkins,Natalia Kraeva,Ognoon Mungunsukh,(unknown),Sheila Riazi,Rachel L. Robinson,Louis Saddic,Nyamkhishig Sambuughin,Richa Saxena,(unknown),Kathryn M. Stowell,James L. Weber,(unknown),Henry Rosenberg,Leslie G. Biesecker	15
4	Orofacial overgrowth with peripheral nerve enlargement and perineuriomatous pseudo-onion bulb proliferations is part of the PIK3CA-related overgrowth spectrum 2020 ·SHILAP Revista de lepidopterología ·Ioannis G. Koutlas,(unknown),(unknown),Ana Sueli Rodrigues Cavalcante,Mohammed Al Kindi,(unknown),Julie C. Sapp,Hannah Kondolf,Marjorie J. Lindhurst,(unknown),Jennifer J. Johnston,(unknown),(unknown),Arupa Ganguly,Leslie G. Biesecker	6
5	NAA10 polyadenylation signal variants cause syndromic microphthalmia 2019 ·Journal of Medical Genetics ·Jennifer J. Johnston,Kathleen A. Williamson,(unknown),Julie C. Sapp,Morad Ansari,Heather Chapman,D.N. Cooper,Tabib Dabir,(unknown),Richard Holt,Nicola Ragge,Alejandro A. Schäffer,Shurjo K. Sen,Anne Slavotinek,David Fitzpatrick,Thomas Gläser,Fiona Stewart,Graeme C. Black,Leslie G. Biesecker	22
6	Disclosure of cardiac variants of uncertain significance results in an exome cohort 2018 ·Clinical Genetics ·Tokunbor A. Lawal,Katie L. Lewis,Jennifer J. Johnston,(unknown),David Ng,F. Gaston‐Johansson,William M. P. Klein,Barbara B. Biesecker,Leslie G. Biesecker	14
7	Recurrent, Activating Variants in the Receptor Tyrosine Kinase DDR2 Cause Warburg-Cinotti Syndrome 2018 ·The American Journal of Human Genetics ·(unknown),Hanne Jensen,Jennifer J. Johnston,Emilio Di Maria,Katja Kloth,(unknown),Julie C. Sapp,Thomas N. Darling,Laryssa A. Huryn,Lisbeth Tranebjærg,Élisa Cinotti,Christian Kubisch,Eyvind Rødahl,Ove Bruland,Leslie G. Biesecker,Gunnar Houge,Cecilie Bredrup	18
8	Health behaviors among unaffected participants following receipt of variants of uncertain significance in cardiomyopathy-associated genes 2018 ·Genetics in Medicine ·(unknown),Katie L. Lewis,Tokunbor A. Lawal,David Ng,Jennifer J. Johnston,Barbara B. Biesecker,Leslie G. Biesecker	4
9	Outcomes of Counseling after Education about Carrier Results: A Randomized Controlled Trial 2018 ·The American Journal of Human Genetics ·Katie L. Lewis,Kendall L. Umstead,Jennifer J. Johnston,(unknown),(unknown),Kristen Fishler,Leslie G. Biesecker,Barbara B. Biesecker	22
10	Assessing the capability of massively parallel sequencing for opportunistic pharmacogenetic screening 2016 ·Genetics in Medicine ·David Ng,Celine Hong,Larry N. Singh,Jennifer J. Johnston,James C. Mullikin,Leslie G. Biesecker	16
11	Individualized Iterative Phenotyping for Genome-wide Analysis of Loss-of-Function Mutations 2015 ·The American Journal of Human Genetics ·Jennifer J. Johnston,Katie L. Lewis,David Ng,Larry N. Singh,(unknown),Carmen C. Brewer,Brian P. Brooks,Isaac Brownell,Fabio Candotti,Stephen G. Gonsalves,(unknown),Heidi H. Kong,Kristina I. Rother,Robert Sokolic,Benjamin D. Solomon,Wadih M. Zein,D.N. Cooper,Peter D. Stenson,James C. Mullikin,Leslie G. Biesecker	43
12	Functional Analysis of a De NovoACTBMutation in a Patient with Atypical Baraitser-Winter Syndrome 2013 ·Human Mutation ·Jennifer J. Johnston,Kuo‐Kuang Wen,Kim M. Keppler‐Noreuil,Melissa McKane,Jessica L. Maiers,(unknown),Julie C. Sapp,Kris A. DeMali,Peter A. Rubenstein,Leslie G. Biesecker	23
13	Massively-parallel sequencing of genes on a single chromosome: a comparison of solution hybrid selection and flow sorting 2013 ·BMC Genomics ·Jamie K. Teer,Jennifer J. Johnston,Sarah L. Anzick,Marbin Pineda,Gary Stone,(unknown),Paul S. Meltzer,James C. Mullikin,Leslie G. Biesecker	4
14	The Phenotype of a Germline Mutation in PIGA: The Gene Somatically Mutated in Paroxysmal Nocturnal Hemoglobinuria 2012 ·The American Journal of Human Genetics ·Jennifer J. Johnston,Andrea Gropman,Julie C. Sapp,Jamie K. Teer,(unknown),(unknown),Xuan Yuan,Zhaohui Ye,Linzhao Cheng,Robert A. Brodsky,Leslie G. Biesecker	110
15	Brain tissue- and region-specific abnormalities on volumetric MRI scans in 21 patients with Bardet-Biedl syndrome (BBS) 2011 ·BMC Medical Genetics ·Kim M. Keppler‐Noreuil,(unknown),Julie C. Sapp,(unknown),Jennifer J. Johnston,Peg Nopoulos,Leslie G. Biesecker	33
16	Massively Parallel Sequencing of Exons on the X Chromosome Identifies RBM10 as the Gene that Causes a Syndromic Form of Cleft Palate 2010 ·The American Journal of Human Genetics ·Jennifer J. Johnston,Jamie K. Teer,Praveen F. Cherukuri,Nancy F. Hansen,Stacie K. Loftus,Karen Chong,James C. Mullikin,Leslie G. Biesecker	120
17	Recurrence risks for Bardet-Biedl syndrome: Implications of locus heterogeneity 2010 ·Genetics in Medicine ·Julie C. Sapp,Darryl Nishimura,Jennifer J. Johnston,Edwin M. Stone,Elise Héon,Val C. Sheffield,Leslie G. Biesecker	11
18	Association of a de novo16q copy number variant with a phenotype that overlaps with Lenz microphthalmia and Townes-Brocks syndromes 2009 ·BMC Medical Genetics ·Tanya Bardakjian,Adele Schneider,David Ng,Jennifer J. Johnston,Leslie G. Biesecker	18
19	Left-sided embryonic expression of the BCL-6 corepressor, BCOR, is required for vertebrate laterality determination 2007 ·Human Molecular Genetics ·Emma Hilton,Forbes Manson,Jill Urquhart,Jennifer J. Johnston,Anne Slavotinek,Peter Hedera,Eva‐Lena Stattin,Ann Nordgren,Leslie G. Biesecker,Graeme C. Black	40
20	Gonadal mosaicism in severe Pallister–Hall syndrome 2003 ·American Journal of Medical Genetics Part A ·David Ng,Jennifer J. Johnston,Joyce Turner,Eilis Boudreau,Edythe Wiggs,William H. Theodore,Leslie G. Biesecker	17

About Jennifer J. Johnston

Jennifer J. Johnston is a scholar working on Genetics, Immunology and Allergy and Genetics, having authored 55 papers that have together received 3.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), Hedgehog Signaling Pathway Studies (9 papers) and Genetic and Kidney Cyst Diseases (8 papers). The work is most often cited by research in Endocrine and Autonomic Systems (279 citations), Genetics (1.1k citations) and Pharmacology (478 citations). Jennifer J. Johnston has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Leslie G. Biesecker, Joseph Dinchuk, James M. Trzăskos, Bruce D. Car, Vicki M. Eng, Nancy Contel, Bruce Jaffee, Richard J. Focht, Robert J. Collins and Maryanne Covington. Their work appears in journals such as Nature, Journal of Biological Chemistry and SHILAP Revista de lepidopterología.

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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