Concepedia

Author

Kathryn L. Lunetta

Boston UniversityORCID

Also Known As

A.P. Lieberman, Ambrosone, C.B., Ambrosone, Christine B., Ambs, S., Andrew P Lieberman, Aulchenko, Yurii S., Bandera, Elisa V., Bensen, Jeannette T., Blot, W., Castro-Webb, Nelsy

614

Publications

53.4K

Citations

98

H-Index

196

Concepts

All Affiliations

Boston UniversityFramingham Heart StudyHarvard UniversityNational Heart Lung and Blood InstituteMassachusetts General Hospital
KL

About

Kathryn L. Lunetta is an author at Boston University specializing in medicine, genetics, and public health.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

35

56

8.1K

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Health Sciences

3

3

172

3

Engineering

2

2

644

4

Natural Sciences

2

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99

5

Education

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448

Kathryn L. Lunetta

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217

Publications

28.1K

Citations

71

H-Index

YearCitations

New insights into the genetic etiology of Alzheimer’s disease and related dementias

Céline Bellenguez, Fahri Küçükali, Iris E. Jansen,

Nature Genetics

2022

2.3K

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Daniel Taliun, Daniel Harris, Michael D. Kessler,

Nature

2021

2.2K

Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease

Valentina Escott‐Price, Céline Bellenguez, Li‐San Wang,

PLoS ONE

2014

1.4K

Common variants at 30 loci contribute to polygenic dyslipidemia

Sekar Kathiresan, Cristen J. Willer, Gina M. Peloso,

Nature Genetics

2008

1.4K

DNA methylation age of blood predicts all-cause mortality in later life

Riccardo E. Marioni, Sonia Shah, Allan F. McRae,

Genome Biology

2015

1.3K

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

Ekaterina Rogaeva, Yan Meng, Joseph H. Lee,

Nature Genetics

2007

1.2K

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Alexander G. Bick, Joshua S. Weinstock, Satish K. Nandakumar,

Nature

2020

698

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

Bruce M. Psaty, Christopher J. O’Donnell, Vilmundur Guðnason,

Circulation Cardiovascular Genetics

2009

605

PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden Syndrome

Deborah J. Marsh, Jennifer B. Kum, Kathryn L. Lunetta,

Human Molecular Genetics

1999

605

Common variants in KCNN3 are associated with lone atrial fibrillation

Patrick T. Ellinor, Kathryn L. Lunetta, Nicole L. Glazer,

Nature Genetics

2010

480

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