Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

Annika M. Dries · SciRah

Researcher profile · Semantic Scholar

Annika M. Dries

Share profile

Annika M. Dries — researcher profile on SciRah

h-index: 15
Works: 24
Citations: 1,192

Most-cited papers

Effect of Moderate-Intensity Exercise Training on Peak Oxygen Consumption in Patients With Hypertrophic Cardiomyopathy: A Randomized Clinical Trial
S. Saberi, M. Wheeler, J. Bragg-Gresham, W. Hornsby +12 more
2017Journal of the American Medical Association (JAMA)228 citations Open access
Semantic Scholar
MARRVEL: Integration of Human and Model Organism Genetic Resources to Facilitate Functional Annotation of the Human Genome.
Julia Wang, Rami Al-ouran, Yan-Hui Hu, Seon-Young Kim +180 more
2017American Journal of Human Genetics194 citations Open access
Semantic Scholar
The Undiagnosed Diseases Network: Accelerating Discovery about Health and Disease.
R. Ramoni, J. Mulvihill, David R. Adams, Patrick Allard +175 more
2017American Journal of Human Genetics177 citations Open access
Semantic Scholar
A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3.
Hsiao-Tuan Chao, M. Davids, Elizabeth A. Burke, J. Pappas +176 more
2017American Journal of Human Genetics111 citations Open access
Semantic Scholar
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder
M. Oláhová, W. Yoon, K. Thompson, S. Jangam +209 more
2018American Journal of Human Genetics91 citations Open access
Semantic Scholar
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype.
V. Shashi, L. Pena, Katherine H. Kim, B. Burton +191 more
2016American Journal of Human Genetics58 citations Open access
Semantic Scholar
Yield of Whole Exome Sequencing in Undiagnosed Patients Facing Insurance Coverage Barriers to Genetic Testing
C. Reuter, Jennefer N. Kohler, D. Bonner, Diane B. Zastrow +25 more
2019Journal of Genetic Counseling53 citations Open access
Semantic Scholar
Genotype–phenotype correlations in individuals with pathogenic RERE variants
Valerie K. Jordan, Brieana Fregeau, Xiaoyan Ge, J. Giordano +25 more
2018Human Mutation46 citations Open access
Semantic Scholar
De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder
G. Mirzaa, Jessica X. Chong, A. Piton, B. Popp +72 more
2019Genetics in Medicine41 citations Open access
Semantic Scholar
The Genetic Architecture of Plakophilin 2 Cardiomyopathy
Annika M. Dries, A. Kirillova, C. Reuter, John Garcia +29 more
2021Genetics in Medicine30 citations Open access
Semantic Scholar
Extracutaneous Manifestations in Phacomatosis Cesioflammea and Cesiomarmorata: Case Series and Literature Review
Akash Kumar, Diane B. Zastrow, E. Kravets, Daniah T Beleford +16 more
2019American Journal of Medical Genetics. Part A25 citations Open access
Semantic Scholar
Intrinsic Atrial Myopathy Precedes Left Ventricular Dysfunction and Predicts Atrial Fibrillation in Lamin A/C Cardiomyopathy
M. Tremblay-Gravel, K. Ichimura, K. Picard, Y. Kawano +5 more
2022Circulation Genomic and Precision Medicine24 citations Open access
Semantic Scholar
Whole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice‐site and Charcot‐Marie‐Tooth phenotype with early onset symptoms
T. Cassini, L. Duncan, Lynette C. Rives, J. Newman +177 more
2019Molecular Genetics & Genomic Medicine24 citations Open access
Semantic Scholar
Effects of Vigorous Versus Restorative Yoga Practice on Objective Cognition Functions in Sedentary Breast and Ovarian Cancer Survivors: A Randomized Controlled Pilot Trial
Gary Deng, T. Bao, Elizabeth L. Ryan, Lara Benusis +6 more
2022Integrative Cancer Therapies15 citations Open access
Semantic Scholar
IgG4‐related disease: Association with a rare gene variant expressed in cytotoxic T cells
J. Newman, Aaron C. Shaver, Jonathan H. Sheehan, S. Mallal +208 more
2019Molecular Genetics & Genomic Medicine15 citations Open access
Semantic Scholar
Clinical and genetic risk factors for aromatase inhibitor-associated arthralgia in breast cancer survivors
Sally A. D. Romero, H. I. Su, J. Satagopan, Q. Li +4 more
2019Breast14 citations Open access
Semantic Scholar
A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network
Chloe M. Reuter, Elise Brimble, Colette DeFilippo, Annika M. Dries +5 more
2018Jornal de Pediatria14 citations Open access
Semantic Scholar
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students
Megan E. Grove, Shana White, D. Fisk, Shannon Rego +200 more
2019Journal of Genetic Counseling12 citations Open access
Semantic Scholar
A Patient with Sjogren’s Syndrome and Subsequent Diagnosis of Inclusion Body Myositis and Light-Chain Amyloidosis
J. Hom, S. Marwaha, Anna Postolova, Jessie Kittle +15 more
2019Journal of general internal medicine7 citations Open access
Semantic Scholar
Exome sequencing identifies de novo pathogenic variants in FBN1 and TRPS1 in a patient with a complex connective tissue phenotype
Diane B. Zastrow, Patricia A. Zornio, Annika M. Dries, Jennefer N. Kohler +10 more
2017Cold Spring Harbor molecular case studies7 citations Open access
Semantic Scholar
Arrhythmogenic Cardiomyopathy: Mechanisms, Genetics, and Their Clinical Implications
Chloe M. Reuter, Annika M. Dries, V. Parikh
2021Current Cardiovascular Risk Reports4 citations
Semantic Scholar
Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy
Annika M. Dries, A. Kirillova, Chloe M. Reuter, John Garcia +29 more
2021Genetics in Medicine2 citations Open access
Semantic Scholar
A resource of lipidomics and metabolomics data from individuals with undiagnosed diseases
J. Kyle, K. Stratton, Erika M. Zink, Young-Mo Kim +202 more
2021Scientific Data1 citations Open access
Semantic Scholar
Abstract 15382: Variant Subtype and Regionality Aid Assessment of Pathogenicity in Plakophillin-2 ( PKP2 )
Annika M. Dries, A. Kirillova, Chloe M. Reuter, Hana Zouk +8 more
20200 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

Jennefer N. Kohler×15
Invite
Jennefer N. Kohler — researcher profile on SciRah
Ya-Ping Yang×12
Invite
Ya-Ping Yang — researcher profile on SciRah
D. Waggott×11
Invite
D. Waggott — researcher profile on SciRah
J. Krier×10
Invite
J. Krier — researcher profile on SciRah

Ellen F. Macnamara

×10

Invite

Ellen F. Macnamara — researcher profile on SciRah

Invite

L. Rodan — researcher profile on SciRah

Invite

K. Schoch — researcher profile on SciRah

Invite

V. Shashi — researcher profile on SciRah

R. Spillmann×10

Invite

R. Spillmann — researcher profile on SciRah

D. Sweetser×10

Invite

D. Sweetser — researcher profile on SciRah

Invite

M. Wangler — researcher profile on SciRah

H. Barseghyan×9

Invite

H. Barseghyan — researcher profile on SciRah