Margaret G. Ehm

11.4k citations

43 papers · 3.3k indexed · 1 hit paper · h-index 25

Genetics top 1%
- Genetic Associations and Epidemiology 26
- Genomics and Rare Diseases 11
- Genetic Mapping and Diversity in Plants and Animals 9
- Genetics and Neurodevelopmental Disorders 4
- Evolution and Genetic Dynamics 3
Endocrine and Autonomic Systems top 5%
Physiology top 5%
Molecular Biology top 10%
- Bioinformatics and Genomic Networks 5
Endocrinology, Diabetes and Metabolism top 5%
Pharmacology
- Pharmacogenetics and Drug Metabolism 4
Oncology
- Drug Transport and Resistance Mechanisms 2

Co-authors: Michael J. Wagner Dmitri V. Zaykin B. S. Weir Dahlia M. Nielsen Peter H. Westfall Daniel K. Burns Matthew R. Nelson H. Sakul
Cited by: Genetics Endocrine and Autonomic Systems Physiology
Journals: Journal of Clinical Investigation (1 paper)Journal of Clinical Oncology (1 paper)PLoS ONE (4 papers)
Partner nations: United States United Kingdom Australia

In The Last Decade

Margaret G. Ehm

42 papers receiving 3.3k citations

Hit Papers

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Peers

Countries citing papers authored by Margaret G. Ehm

Since Specialization

Citations

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

Fields of papers citing papers by Margaret G. Ehm

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Margaret G. Ehm. 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 Margaret G. Ehm. The network helps show where Margaret G. Ehm may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Meta-Analysis of 26 638 Individuals Identifies Two Genetic Loci Associated With Left Ventricular Ejection Fraction Circulation Genomic and Precision Medicine ·Hélène Choquet,Khanh K. Thai,J Chen,Dilrini K. Ranatunga,Thomas J. Hoffmann,Alan S. Go,Alistair C Lindsay,Margaret G. Ehm,Dawn Waterworth,Neil Risch,Catherine Schaefer	2020	14
2	Characterization of ADME gene variation in 21 populations by exome sequencing Pharmacogenetics and Genomics ·Daniel H. Hovelson,Zhengyu Xue,Matthew Zawistowski,Margaret G. Ehm,E Clare Harris,Sophie L. Stocker,Annette S. Gross,In‐Jin Jang,Ichiro Ieiri,Jong Eun Lee,Lon R. Cardon,Stephanie L. Chissoe,Gonçalo R. Abecasis,Matthew R. Nelson	2016	34
3	Comparing variant calling algorithms for target-exon sequencing in a large sample BMC Bioinformatics ·Yancy Lo,Hyun Min Kang,Matthew R. Nelson,Mohammad Othman,Stephanie L. Chissoe,Margaret G. Ehm,Gonçalo R. Abecasis,Sebastian Zöllner	2015	3
4	The Benefits of Using Genetic Information to Design Prevention Trials The American Journal of Human Genetics ·Youna Hu,Li Li,Margaret G. Ehm,Nan Bing,Kijoung Song,Matthew R. Nelson,Philippa J. Talmud,Aroon D. Hingorani,Meena Kumari,Mika Kivimäki,Chun‐Fang Xu,Dawn Waterworth,John C. Whittaker,Gonçalo R. Abecasis,Cathie Spino,Hyun Min Kang	2013	14
5	Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families PLoS ONE ·Carlos Cruchaga,Sumitra Chakraverty,Kevin H. Mayo,Francesco Vallania,Robi D. Mitra,Kelley Faber,Jennifer Williamson,T. Bird,Ramon Diaz‐Arrastia,Tatiana Foroud,Bradley F. Boeve,Neill R. Graff‐Radford,Pamela St. Jean,Michael J. Lawson,Margaret G. Ehm,Richard Mayeux,Alison Goate	2012	206
6	Correction: Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families PLoS ONE ·Carlos Cruchaga,Sumitra Chakraverty,Kevin H. Mayo,Francesco Vallania,Robi D. Mitra,Kelley Faber,Jennifer Williamson,Thomas G. Bird,Ramon Diaz‐Arrastia,Tatiana Foroud,Bradley F. Boeve,Neill R. Graff‐Radford,Pamela St. Jean,Michael J. Lawson,Margaret G. Ehm,Richard Mayeux,Alison Goate	2012	30
7	Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes PLoS ONE ·Li Li,Yun Li,Sharon R. Browning,Brian L. Browning,Andrew J. Slater,Xiangyang Kong,Jennifer L. Aponte,Vincent Mooser,Stephanie L. Chissoe,John C. Whittaker,Matthew R. Nelson,Margaret G. Ehm	2011	40
8	Comparison of association methods for dense marker data Genetic Epidemiology ·Silviu‐Alin Bacanu,Matthew R. Nelson,Margaret G. Ehm	2008	11
9	Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions The Pharmacogenomics Journal ·Matthew R. Nelson,Silviu‐Alin Bacanu,Michael Mosteller,Ling-Ling Li,Clive Bowman,A D Roses,Eric Lai,Margaret G. Ehm	2008	69
10	On the utility of data from the International HapMap Project for Australian association studies Human Genetics ·Jim Stankovich,Charles Cox,Rachel B. Tan,Douglas S. Montgomery,Stewart Huxtable,Justin P. Rubio,Margaret G. Ehm,Laura Johnson,Helmut Butzkueven,Trevor J. Kilpatrick,Terence P. Speed,Allen D. Roses,Melanie Bahlo,Simon J. Foote	2006	17
11	Guidelines for conducting and reporting whole genome/large-scale association studies Human Molecular Genetics ·Margaret G. Ehm,Matthew R. Nelson,Nigel K. Spurr	2005	10
12	Case‐control single‐marker and haplotypic association analysis of pedigree data Genetic Epidemiology ·Sharon R. Browning,J. D. Briley,Linda P. Briley,Gyan Chandra,Jonathan H. Charnecki,Margaret G. Ehm,Kelley A. Johansson,Brendan Jones,Andrew J. Karter,David P. Yarnall,Michael J. Wagner	2004	41
13	Linkage Analysis Using Single Nucleotide Polymorphisms Human Heredity ·Brian L. Browning,Donna L. Brashear,Andy A. Butler,Devon D. Cyr,E Clare Harris,Anita J. Nelsen,David P. Yarnall,Margaret G. Ehm,Michael J. Wagner	2004	8
14	Selection of Genetic Markers for Association Analyses, Using Linkage Disequilibrium and Haplotypes The American Journal of Human Genetics ·Zhaoling Meng,Dmitri V. Zaykin,Chun‐Fang Xu,Michael J. Wagner,Margaret G. Ehm	2003	114
15	Testing Association of Statistically Inferred Haplotypes with Discrete and Continuous Traits in Samples of Unrelated Individualsbreakdown → Human Heredity ·Dmitri V. Zaykin,Peter H. Westfall,S Stanley Young,Maha A. Karnoub,Michael J. Wagner,Margaret G. Ehm	2002	547
16	Genome-Wide Scan of Obesity in the Old Order Amish¹ The Journal of Clinical Endocrinology & Metabolism ·Wen‐Chi Hsueh,Braxton D. Mitchell,Jennifer L. Schneider,Pamela L. St. Jean,Toni I. Pollin,Margaret G. Ehm,Michael Wagner,Daniel K. Burns,H. Sakul,Callum J. Bell,Alan R. Shuldiner	2001	68
17	Migraine with Aura Susceptibility Locus on Chromosome 19p13 Is Distinct from the Familial Hemiplegic Migraine Locus Genomics ·Keith Jones,Margaret G. Ehm,Margaret A. Pericak‐Vance,Jonathan L. Haines,Peter R. Boyd,Stephen J. Peroutka	2001	55
18	Autosomal Genomic Scan for Loci Linked to Obesity and Energy Metabolism in Pima Indians The American Journal of Human Genetics ·Rachel Norman,P. Antonio Tataranni,Richard E. Pratley,D B Thompson,Robert L. Hanson,Michal Procházka,Leslie J. Baier,Margaret G. Ehm,H. Sakul,Tatiana Foroud,W. Timothy Garvey,David K Burns,William C. Knowler,Peter H. Bennett,Clifton Bogardus,Éric Ravussin	1998	146
19	Detecting Marker-Disease Association by Testing for Hardy-Weinberg Disequilibrium at a Marker Locus The American Journal of Human Genetics ·Dahlia M. Nielsen,Margaret G. Ehm,B. S. Weir	1998	283
20	An Autosomal Genomic Scan for Loci Linked to Type II Diabetes Mellitus and Body-Mass Index in Pima Indians The American Journal of Human Genetics ·Robert L. Hanson,Margaret G. Ehm,David J. Pettitt,Michal Procházka,D B Thompson,David S. Timberlake,Tatiana Foroud,Sayuko Kobes,Leslie J. Baier,Daniel K. Burns,Laura Almasy,John Blangero,W. Timothy Garvey,Peter H. Bennett,William C. Knowler	1998	382

About Margaret G. Ehm

Margaret G. Ehm is a scholar working on Genetics, Pharmacology and Endocrine and Autonomic Systems, having authored 43 papers that have together received 3.3k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (26 papers), Genomics and Rare Diseases (11 papers), Genetic Mapping and Diversity in Plants and Animals (9 papers), Bioinformatics and Genomic Networks (5 papers), Pharmacogenetics and Drug Metabolism (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Evolution and Genetic Dynamics (3 papers) and Drug Transport and Resistance Mechanisms (2 papers). The work is most often cited by research in Genetics (1.7k citations), Endocrine and Autonomic Systems (193 citations) and Physiology (659 citations). Margaret G. Ehm has collaborated with scholars based in United States, United Kingdom and Australia. Frequent co-authors include Michael J. Wagner, Dmitri V. Zaykin, B. S. Weir, Dahlia M. Nielsen, Peter H. Westfall, Daniel K. Burns, Matthew R. Nelson, H. Sakul, William C. Knowler and D B Thompson. Their work appears in journals such as Journal of Clinical Investigation, Journal of Clinical Oncology and PLoS ONE.

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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