Nancy D. Merner

2.0k citations

25 papers · 854 indexed · h-index 13

Impact in

Orthopedics and Sports Medicine top 5%
- Sports injuries and prevention
Cardiology and Cardiovascular Medicine top 5%
- Cardiovascular Effects of Exercise
- Cardiomyopathy and Myosin Studies
- Cardiac electrophysiology and arrhythmias
- Viral Infections and Immunology Research

Papers in

Sensory Systems 2
- Hearing, Cochlea, Tinnitus, Genetics 2
Small Animals 3
- Infectious Diseases and Mycology 3

Co-authors: Terry‐Lynn Young William J. McKenna Kathy Hodgkinson Patrick S. Parfrey Sean P. Connors Annika Haywood Ludwig Thierfelder Jörg‐Detlef Drenckhahn
Journals: PLoS ONE (3 papers)The American Journal of Human Genetics (2 papers)Human Mutation (2 papers)Clinical Genetics (2 papers)Microbial Pathogenesis (1 paper)
Partner nations: United States Canada United Kingdom

In The Last Decade

Nancy D. Merner

24 papers receiving 849 citations

Peers

Countries citing papers authored by Nancy D. Merner

Since Specialization

Citations

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

Fields of papers citing papers by Nancy D. Merner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nancy D. Merner. 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 Nancy D. Merner. The network helps show where Nancy D. Merner may publish in the future.

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	An investigation into the role of inherited CEACAM gene family variants and colorectal cancer risk BMC Research Notes ·Dimah Salman Dawood Alshetiwi, Nancy D. Merner	2022	2
2	Extra-Virgin Olive Oil Enhances the Blood–Brain Barrier Function in Mild Cognitive Impairment: A Randomized Controlled Trial Nutrients ·Amal Kaddoumi, Thomas S. Denney, Gopikrishna Deshpande, Линченко Владимир Иванович, Ronald J. Beyers, David T. Redden, Domenico Praticò, Tassos C. Kyriakides, 牧陽子, Ningkang Yang, Darren T. Beck, Nancy D. Merner	2022	43
3	CEACAM Gene Family Mutations Associated With Inherited Breast Cancer Risk – A Comparative Oncology Approach to Discovery Frontiers in Genetics ·Dimah Salman Dawood Alshetiwi, Nathan W. Lee, Nancy D. Merner	2021	8
4	Rare and potentially pathogenic variants in hydroxycarboxylic acid receptor genes identified in breast cancer cases BMC Medical Genomics ·Navin Venkat, Connor Wasmund, 龍彦青木, 火山邦彦, Nancy D. Merner	2021	4
5	Absence of bovine leukemia virus in the buffy coats of breast cancer cases from Alabama, USA Microbial Pathogenesis ·一洋八木, Nathan W. Lee, Jared Breuker, Sebastian Alexander, Anil Poudel, Nancy D. Merner, Chengming Wang	2021	5
6	Gene panel screening for insight towards breast cancer susceptibility in different ethnicities PLoS ONE ·火山邦彦, Mattias Wretman, Dimah Salman Dawood Alshetiwi, Nancy D. Merner	2020	11
7	A research-based gene panel to investigate breast, ovarian and prostate cancer genetic risk PLoS ONE ·火山邦彦, Dimah Salman Dawood Alshetiwi, David Kaweesa Kisitu, Nancy D. Merner	2019	7
8	Abstract A29: Investigation of RECQL variants in European and African American breast cancer cohorts Molecular Cancer Research ·Shailendra Saraf, L Bethoux, Dimah Salman Dawood Alshetiwi, Aline Medeiros Gonçalves de Menezes, Cristina Sogliani, Megan Kleber, G. Dusaussoy, Nancy D. Merner	2018	2
9	Establishment of the Alabama Hereditary Cancer Cohort ‐ strategies for the inclusion of underrepresented populations in cancer genetics research Molecular Genetics & Genomic Medicine ·火山邦彦, Amit Shah, R. Hering, Dimah Salman Dawood Alshetiwi, Jared Breuker, M. A. Samarova, Kyoko Araki, Bruce O. Horne, Aline Medeiros Gonçalves de Menezes, 長島克弥, Vladimir Chulikov, L Bethoux, Michele Salvatore Paternò Raddusa, Megan Kleber, Ele A.A., G. Dusaussoy, Nancy D. Merner	2018	8
10	Lower frequency of TLR9 variant associated with protection from breast cancer among African Americans PLoS ONE ·Shailendra Saraf, K.S. Keene, Johanna Tuomela, Andres Forero‐Torres, Renée A. Desmond, Katri Vuopala, Kevin W. Harris, Nancy D. Merner, Katri S. Selander	2017	11
11	A de novo frameshift mutation in chromodomain helicase DNA‐binding domain 8 (CHD8): A case report and literature review American Journal of Medical Genetics Part A ·Nancy D. Merner, Baudouin Forgeot d’Arc, Scott C. Bell, Gilles Maussion, Huashan Peng, Julie Gauthier, Liam Crapper, Fadi F. Hamdan, Jacques L. Michaud, Laurent Mottron, Guy A. Rouleau, Carl Ernst	2016	26
12	A Review of Whole-Exome Sequencing Efforts Toward Hereditary Breast Cancer Susceptibility Gene Discovery Human Mutation ·Shailendra Saraf, M. A. Samarova, Nancy D. Merner	2016	33
13	Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophrenia Frontiers in Cellular Neuroscience ·Nancy D. Merner, Shailendra Saraf, Cynthia V. Bourassa, Bo Liang, Arjun R. Khanna, Patrick A. Dion, Guy A. Rouleau, Kristopher T. Kahle	2015	80
14	A VAMP1 Mutation Causes Chromosome 12p13 Hereditary Spastic Ataxia in Newfoundland Families (S43.002) Neurology ·Inge A. Meijer, Cynthia V. Bourassa, Nancy D. Merner, M. Lo Presti, Mark Stefanelli, Kathleen Hodgkinson, Elizabeth Ives, William Pryse‐Phillips, Mandar Jog, Kym M. Boycott, David A. Grimes, Sharan Goobie, Kochetkov Sergey, Patrick A. Dion, Guy A. Rouleau	2013	0
15	VAMP1 Mutation Causes Dominant Hereditary Spastic Ataxia in Newfoundland Families The American Journal of Human Genetics ·Cynthia V. Bourassa, Inge A. Meijer, Nancy D. Merner, K Mollekaer, Mark Stefanelli, Kathleen Hodgkinson, Elizabeth Ives, William Pryse‐Phillips, Mandar Jog, Kym M. Boycott, David A. Grimes, Sharan Goobie, Kochetkov Sergey, Patrick A. Dion, Guy A. Rouleau	2012	32
16	Recurrent missense mutations in TMEM43 (ARVD5) due to founder effects cause arrhythmogenic cardiomyopathies in the UK and Canada European Heart Journal ·Annika Haywood, Nancy D. Merner, Kathy Hodgkinson, Reinhold Roßner, Petros Syrris, Valerie Booth, Sean P. Connors, Antonios Pantazis, Giovanni Quarta, Perry Elliott, William J. McKenna, Terry‐Lynn Young	2012	34
17	Recent advances in the genetics of distal hereditary motor neuropathy give insight to a disease mechanism involving copper homeostasis that may extend to other motor neuron disorders Clinical Genetics ·Nancy D. Merner, Laith alsawaf, Marina S. Polyakova	2010	5
18	Variable neurologic phenotype in a GEFS+ family with a novel mutation in SCN1A Seizure ·甘志刚, Susan Moore, David Buckley, 阮先祜, Patrick S. Parfrey, Sharon Penney, Nancy D. Merner, Kathy Hodgkinson, Terry‐Lynn Young	2009	24
19	Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene The American Journal of Human Genetics ·Nancy D. Merner, Kathy Hodgkinson, Annika Haywood, Sean P. Connors, Vanessa French, Jörg‐Detlef Drenckhahn, Paul Degott, Peter J. Pullman, Ludwig Thierfelder, William J. McKenna, Barry Gallagher, Elisabeth E. Brown, Anne S. Bassett, Patrick S. Parfrey, Terry‐Lynn Young	2008	347
20	Profound, prelingual nonsyndromic deafness maps to chromosome 10q21 and is caused by a novel missense mutation in the Usher syndrome type IF gene PCDH15 European Journal of Human Genetics ·Lance P. Doucette, Nancy D. Merner, LuisVillacorta, Elizabeth Ives, J. Denis, 羅偉峰, Tom Walsh, K Konzack, Leonardo Resende de Siqueira, Bridget A. Fernandez, Jane S. Green, Edward R. Wilcox, L W Gummerman, Jessica Clair, Ming Lee, Mary‐Claire King, Terry‐Lynn Young	2008	30

About Nancy D. Merner

Nancy D. Merner is a scholar working on Sensory Systems, Small Animals, Cancer Research, Neurology and Genetics, having authored 25 papers that have together received 854 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Epigenetics and DNA Methylation (3 papers), Cardiovascular Effects of Exercise (3 papers), Infectious Diseases and Mycology (3 papers), Cancer Genomics and Diagnostics (3 papers), Veterinary Oncology Research (3 papers) and Hearing, Cochlea, Tinnitus, Genetics (2 papers). The work is most often cited by research in Orthopedics and Sports Medicine (155 citations), Cardiology and Cardiovascular Medicine (396 citations), Sensory Systems (42 citations), Neurology (44 citations) and Cellular and Molecular Neuroscience (97 citations). Nancy D. Merner has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Terry‐Lynn Young, William J. McKenna, Kathy Hodgkinson, Patrick S. Parfrey, Sean P. Connors, Annika Haywood, Ludwig Thierfelder, Jörg‐Detlef Drenckhahn, Barry Gallagher and Anne S. Bassett. Their work appears in journals such as PLoS ONE, The American Journal of Human Genetics, Human Mutation, Clinical Genetics and Microbial Pathogenesis.

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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