Hutton M. Kearney

5.8k citations

40 papers · 3.2k indexed · 3 hit papers · h-index 21

Impact in

Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Pediatrics, Perinatology and Child Health top 1%
- Prenatal Screening and Diagnostics
- Fetal and Pediatric Neurological Disorders

Papers in

Genetics 26
- Genomic variations and chromosomal abnormalities 20
- Genomics and Rare Diseases 16
Pediatrics, Perinatology and Child Health 13
- Prenatal Screening and Diagnostics 13

Co-authors: Sarah T. South Erik C. Thorland Fabiola Quintero‐Rivera Kerry K. Brown Athena M. Cherry Sibel Kantarci Swaroop Aradhya Erin Rooney Riggs
Journals: Genetics in Medicine (12 papers)Genetics (3 papers)PLoS Genetics (2 papers)npj Genomic Medicine (1 paper)Blood Advances (1 paper)
Partner nations: United States Canada China

In The Last Decade

Hutton M. Kearney

38 papers receiving 3.1k citations

Hit Papers

align trajectories log scale

Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG) 2021 · 288 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2021 Genetics in Medicine
2019 Genetics in Medicine
2011 Genetics in Medicine

Peers

Countries citing papers authored by Hutton M. Kearney

Since Specialization

Citations

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

Fields of papers citing papers by Hutton M. Kearney

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hutton M. Kearney. 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 Hutton M. Kearney. The network helps show where Hutton M. Kearney may publish in the future.

Co-authors

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

All Works

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

20 of 20 papers shown

#	Work
1	Updated recommendations for CFTR carrier screening: A position statement of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Joshua L. Deignan, Anthony R. Gregg, Wayne W. Grody, Michael H. Guo, Hutton M. Kearney, Kristin G. Monaghan, Karen S. Raraigh, Jennifer Taylor, Cinthya Zepeda‐Mendoza, Catherine A. Ziats	2023	18
2	P589: Improved efficiency of G-band chromosome analysis via deep neural network workflow SHILAP Revista de lepidopterología ·Xinjie Xu, Derek Slagter, Todd VanDeWalker, Erin Theobald, Tina L. Brown, Daniel Hoppe, Sheryl Castro, Joel Denney, Jennifer M. Gardner, Christopher C. Stahl, Hutton M. Kearney, Jansen N. Seheult, Carley Ann Suarez, Harshawardhan Banda	2023	1
3	Alström syndrome caused by maternal uniparental disomy American Journal of Ophthalmology Case Reports ·Madeline Q.R. Lopour, Lisa A. Schimmenti, Nicole J. Boczek, Hutton M. Kearney, Arlene V. Drack, Michael C. Brodsky	2022	0
4	Lymphoid blast transformation in an MPN with BCR-JAK2 treated with ruxolitinib: putative mechanisms of resistance Blood Advances ·Justin Anthony Chen, Yanli Hou, Krishna M. Roskin, Daniel A. Arber, Charles D. Bangs, Linda B. Baughn, Athena M. Cherry, Mark D. Ewalt, Andrew Fire, Laure Frésard, Hutton M. Kearney, Stephen B. Montgomery, Robert S. Ohgami, Kathryn E. Pearce, Beth A. Pitel, Jason D. Merker, Jason Gotlib	2021	14
5	Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Kandamurugu Manickam, Monica R. McClain, Laurie Demmer, Sawona Biswas, Hutton M. Kearney, Jennifer Malinowski, Lauren Massingham, Danny E. Miller, Timothy W. Yu, Fuki M. Hisama Hit paper breakdown →	2021	288
6	Best practices for the analytical validation of clinical whole-genome sequencing intended for the diagnosis of germline disease npj Genomic Medicine ·Christian R. Marshall, Shimul Chowdhury, Ryan J. Taft, Matthew S. Lebo, Jillian G. Buchan, Steven M. Harrison, Ross Rowsey, Eric W. Klee, Pengfei Liu, Elizabeth A. Worthey, Vaidehi Jobanputra, David Dimmock, Hutton M. Kearney, David Bick, Shashikant Kulkarni, Stacie L. Taylor, John W. Belmont, Dimitri J. Stavropoulos, Niall J. Lennon	2020	85
7	The Medical Genome Initiative: moving whole-genome sequencing for rare disease diagnosis to the clinic Genome Medicine ·Christian R. Marshall, David Bick, John W. Belmont, Stacie L. Taylor, Euan A. Ashley, David Dimmock, Vaidehi Jobanputra, Hutton M. Kearney, Shashikant Kulkarni, Heidi L. Rehm	2020	27
8	Mate pair sequencing outperforms fluorescence in situ hybridization in the genomic characterization of multiple myeloma Blood Cancer Journal ·James B. Smadbeck, Jess F. Peterson, Kathryn E. Pearce, Beth A. Pitel, Andrea Lebron Figueroa, Michael Timm, Dragan Jevremović, Min Shi, A. Keith Stewart, Esteban Braggio, Daniel L. Riggs, P. Leif Bergsagel, George Vasmatzis, Hutton M. Kearney, Nicole L. Hoppman, Rhett P. Ketterling, Shaji Kumar, S. Vincent Rajkumar, Patricia T. Greipp, Linda B. Baughn	2019	29
9	Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Joshua L. Deignan, Wendy K. Chung, Hutton M. Kearney, Kristin G. Monaghan, Catherine Rehder, Elizabeth Chao	2019	121
10	Interstitial 4q Deletion Syndrome Including <b><i>NR3C2</i></b> Causing Pseudohypoaldosteronism Molecular Syndromology ·Amanda Barone Pritchard, Alyssa Ritter, Hutton M. Kearney, Kosuke Izumi	2019	4
11	Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen) Genetics in Medicine ·Erin Rooney Riggs, Erica Andersen, Athena M. Cherry, Sibel Kantarci, Hutton M. Kearney, Ankita Patel, Gordana Raca, Deborah Ritter, Sarah T. South, Erik C. Thorland, Daniel Pineda‐Alvarez, Swaroop Aradhya, Alastair J. Martin Hit paper breakdown →	2019	879
12	Use of mate-pair sequencing to characterize a complex cryptic BCR/ABL1 rearrangement observed in a newly diagnosed case of chronic myeloid leukemia Human Pathology ·Jess F. Peterson, Beth A. Pitel, Stephanie A. Smoley, James B. Smadbeck, Sarah H. Johnson, George Vasmatzis, Hutton M. Kearney, Patricia T. Greipp, Nicole L. Hoppman, Linda B. Baughn, Rhett P. Ketterling	2018	6
13	Constitutional chromosome rearrangements that mimic the 2017 world health organization “acute myeloid leukemia with recurrent genetic abnormalities”: A study of three cases and review of the literature Cancer Genetics ·Jess F. Peterson, Beth A. Pitel, Stephanie A. Smoley, James B. Smadbeck, Sarah H. Johnson, George Vasmatzis, Kathryn E. Pearce, Rong He, Katalin Kelemen, Hamid Al‐Mondhiry, Nicholas Lamparella, Nicole L. Hoppman, Hutton M. Kearney, Linda B. Baughn, Rhett P. Ketterling, Patricia T. Greipp	2018	8
14	Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Athena M. Cherry, Yassmine Akkari, Kimberly M. Barr, Hutton M. Kearney, Nancy C. Rose, Sarah T. South, James Tepperberg, Jeanne Meck	2017	29
15	SVAtools for junction detection of genome-wide chromosomal rearrangements by mate-pair sequencing (MPseq) Cancer Genetics ·Sarah H. Johnson, James B. Smadbeck, Stephanie A. Smoley, Athanasios Gaitatzes, Stephen J. Murphy, Faye R. Harris, Travis Drucker, Roman M. Zenka, Beth A. Pitel, Ross Rowsey, Nicole L. Hoppman, Umut Aypar, William R. Sukov, Robert B. Jenkins, Andrew L. Feldman, Hutton M. Kearney, George Vasmatzis	2017	61
16	ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013 Genetics in Medicine ·Sarah T. South, Charles Lee, Allen N. Lamb, Anne W. Higgins, Hutton M. Kearney	2013	232
17	American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing Genetics in Medicine ·Catherine Rehder, Karen L. David, Betsy Hirsch, Helga V. Toriello, Carolyn M. Wilson, Hutton M. Kearney	2013	114
18	American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities Genetics in Medicine ·Hutton M. Kearney, Sarah T. South, Daynna J. Wolff, Allen N. Lamb, Ada Hamosh, Kathleen W. Rao	2011	73
19	Clinical experience with array CGH: Case presentations from nine months of practice American Journal of Medical Genetics Part A ·Alexis F. Poss, Paula Goldenberg, Catherine Rehder, Hutton M. Kearney, Elizabeth C. Melvin, Dwight D. Koeberl, Marie McDonald	2006	7
20	REC, Drosophila MCM8, Drives Formation of Meiotic Crossovers PLoS Genetics ·Hunter L. Blanton, Sarah J. Radford, Susan McMahan, Hutton M. Kearney, Joseph G. Ibrahim, Jeff Sekelsky	2005	75

About Hutton M. Kearney

Hutton M. Kearney is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Hematology, Genetics and Pathology and Forensic Medicine, having authored 40 papers that have together received 3.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Genomics and Rare Diseases (16 papers), Prenatal Screening and Diagnostics (13 papers), Genetic factors in colorectal cancer (6 papers), Acute Myeloid Leukemia Research (6 papers), Acute Lymphoblastic Leukemia research (4 papers), Chromosomal and Genetic Variations (4 papers) and Chronic Myeloid Leukemia Treatments (4 papers). The work is most often cited by research in Genetics (2.2k citations), Pediatrics, Perinatology and Child Health (1.0k citations), Cancer Research (350 citations), Molecular Biology (1.1k citations) and Genetics (174 citations). Hutton M. Kearney has collaborated with scholars based in United States, Canada and China. Frequent co-authors include Sarah T. South, Erik C. Thorland, Fabiola Quintero‐Rivera, Kerry K. Brown, Athena M. Cherry, Sibel Kantarci, Swaroop Aradhya, Erin Rooney Riggs, Ankita Patel and Erica Andersen. Their work appears in journals such as Genetics in Medicine, Genetics, PLoS Genetics, npj Genomic Medicine and Blood Advances.

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