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

B. Cade · SciRah

Researcher profile · Semantic Scholar

B. Cade

Share profile

B. Cade — researcher profile on SciRah

h-index: 45
Works: 203
Citations: 13K

Most-cited papers

The power of genetic diversity in genome-wide association studies of lipids
Sarah E. Graham, S. Clarke, Kuan-Han H. Wu, S. Kanoni +496 more
2021Nature826 citations Open access
Semantic Scholar
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
A. Mahajan, C. Spracklen, Wei-Hua Zhang, M. Ng +345 more
2022Nature Genetics616 citations Open access
Semantic Scholar
Genetic drivers of heterogeneity in type 2 diabetes pathophysiology
Ken Suzuki, K. Hatzikotoulas, L. Southam, H. Taylor +360 more
2024Nature540 citations Open access
Semantic Scholar
Genetic diversity fuels gene discovery for tobacco and alcohol use
Gretchen R. B. Saunders, Xingyan Wang, Fang Chen, Seonkyeong Jang +213 more
2022Nature426 citations Open access
Semantic Scholar
Association of clonal hematopoiesis with chronic obstructive pulmonary disease
P. Miller, D. Qiao, J. Rojas-Quintero, M. Honigberg +40 more
2021Blood207 citations Open access
Semantic Scholar
Clonal hematopoiesis and risk of chronic liver disease
Wai-Hay J. Wong, C. Emdin, A. Bick, S. Zekavat +435 more
2023Nature174 citations Open access
Semantic Scholar
Aberrant activation of TCL1A promotes stem cell expansion in clonal hematopoiesis
J. Weinstock, J. Gopakumar, B. Burugula, M. Uddin +107 more
2023Nature106 citations Open access
Semantic Scholar
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
M. Taub, Matthew P. Conomos, Rebecca Keener, K. Iyer +144 more
2022Cell Genomics67 citations Open access
Semantic Scholar
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
S. Kanoni, Sarah E. Graham, Yuxuan Wang, Ida Surakka +496 more
2022Genome Biology59 citations Open access
Semantic Scholar
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole-genome sequencing studies
Xi-Hao Li, Corbin Quick, Hufeng Zhou, Sheila M. Gaynor +420 more
2022Nature Genetics55 citations Open access
Semantic Scholar
Polygenic prediction of body mass index and obesity through the life course and across ancestries
R. Smit, K. Wade, Qin Hui, J. Arias +496 more
2025Nature Medicine51 citations Open access
Semantic Scholar
Genetic discovery and risk characterization in type 2 diabetes across diverse populations
L. Polfus, B. Darst, H. Highland, Xin Sheng +50 more
2021HGG advances42 citations Open access
Semantic Scholar
Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank
H. Dashti, N. Miranda, B. Cade, Tian-Yi Huang +3 more
2022BMC Medicine39 citations Open access
Semantic Scholar
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
S. Ramdas, Jonathan Judd, Sarah E. Graham, S. Kanoni +496 more
2022American Journal of Human Genetics36 citations Open access
Semantic Scholar
Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.
M. Graff, A. Justice, Kristin L. Young, E. Marouli +221 more
2021American Journal of Human Genetics33 citations Open access
Semantic Scholar
Genetic determinants of cardiometabolic and pulmonary phenotypes and obstructive sleep apnoea in HCHS/SOL
Yuan Zhang, Michael Elgart, N. Kurniansyah, Brian W. Spitzer +10 more
2022EBioMedicine30 citations Open access
Semantic Scholar
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
S. Choi, S. Jurgens, Ling Xiao, M. Hill +496 more
2025Nature Genetics29 citations Open access
Semantic Scholar
Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications
Ken Suzuki, K. Hatzikotoulas, L. Southam, H. Taylor +347 more
2023medRxiv27 citations Open access
Semantic Scholar
Tailoring Risk Prediction Models to Local Populations.
Aniket N. Zinzuwadia, Olga Mineeva, Chunying Li, Zareen M. Farukhi +7 more
2024JAMA cardiology26 citations Open access
Semantic Scholar
Structural variation across 138,134 samples in the TOPMed consortium
G. Jun, A. English, Ginger A. Metcalf, Jianzhi Yang +83 more
2023bioRxiv26 citations Open access
Semantic Scholar
The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections
S. Jones, F. I. Maisha, S. Strausz, B. Cade +9 more
2022medRxiv25 citations Open access
Semantic Scholar
Rare genetic variants explain missing heritability in smoking
Seonkyeong Jang, L. Evans, A. Fialkowski, D. Arnett +86 more
2022Nature Human Behaviour24 citations Open access
Semantic Scholar
Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program.
Xiao-Wei Hu, D. Qiao, Wonji Kim, M. Moll +47 more
2022American Journal of Human Genetics19 citations Open access
Semantic Scholar
Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program
Daniel A. DiCorpo, Sheila M. Gaynor, E. Russell, K. Westerman +89 more
2021Communications Biology18 citations Open access
Semantic Scholar
Pathway-specific Polygenic Risk Scores (PRS) Identify OSA-related Pathways Differentially Moderating Genetic Susceptibility to CAD
M. Goodman, B. Cade, Neomi A. Shah, Tian-Yi Huang +6 more
2022Circulation Genomic and Precision Medicine16 citations Open access
Semantic Scholar
Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate
T. Mack, M. Raddatz, Y. Pershad, D. Nachun +41 more
2024Nature Aging14 citations
Semantic Scholar
Sleep apnea phenotyping and relationship to disease in a large clinical biobank
B. Cade, S. M. Hassan, H. Dashti, Melissa Kiernan +3 more
2022JAMIA Open14 citations Open access
Semantic Scholar
The Genetic Etiology of Periodic Leg Movement in Sleep.
Jacob L. Edelson, L. Schneider, D. Amar, A. Brink-Kjaer +18 more
2022Sleep13 citations Open access
Semantic Scholar
Author Correction: The power of genetic diversity in genome-wide association studies of lipids
Sarah E. Graham, S. Clarke, Kuan-Han H. Wu, S. Kanoni +496 more
2023Nature12 citations Open access
Semantic Scholar
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes
J. Weinstock, C. Laurie, J. Broome, K. Taylor +83 more
2023Science Advances12 citations Open access
Semantic Scholar
Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study
Yuxuan Wang, M. Selvaraj, Xi-Hao Li, Zi-Lin Li +70 more
2023medRxiv11 citations Open access
Semantic Scholar
Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries
A. Huerta-Chagoya, Joohyun Kim, R. Mandla, Ying-Chang Lu +254 more
2025medRxiv9 citations
Semantic Scholar
Obstructive Sleep Apnea and Longitudinal Changes in Interstitial Lung Imaging and Lung Function: The MESA Study.
J. S. Kim, A. Azarbarzin, A. Podolanczuk, Michael R. Anderson +9 more
2023Annals of the American Thoracic Society9 citations Open access
Semantic Scholar
Public health impact of poor sleep on COVID-19, influenza and upper respiratory infections
S. Jones, F. I. Maisha, S. Strausz, B. Cade +8 more
2022Sleep Medicine9 citations Open access
Semantic Scholar
Genome-wide association analysis of composite sleep health scores in 413,904 individuals
M. Goodman, T. Faquih, Valentina Paz, P. Nagarajan +22 more
2025Communications Biology8 citations Open access
Semantic Scholar
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Xi-Hao Li, Han Chen, M. Selvaraj, Eric Van Buren +438 more
2025Nature Computational Science8 citations Open access
Semantic Scholar
Genome-wide association analysis of composite sleep health scores in 413,904 individuals
M. Goodman, T. Faquih, Valentina Paz, P. Nagarajan +22 more
2024medRxiv7 citations Open access
Semantic Scholar
Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes
Rebecca Keener, Surya B. Chhetri, C. Connelly, M. Taub +94 more
2024Nature Communications7 citations Open access
Semantic Scholar
Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
J. Huffman, J. Nicholas, Julie Hahn, Adam S. Heath +132 more
2024Blood7 citations Open access
Semantic Scholar
An integrated multi-omics analysis of sleep-disordered breathing traits implicates P2XR4 purinergic signaling
N. Kurniansyah, Danielle A. Wallace, Y. Zhang, Bing Yu +16 more
2023Communications Biology7 citations Open access
Semantic Scholar
Correlates of daytime sleepiness and insomnia among adults in Samoa
Lacey W. Heinsberg, J. Carlson, A. Pomer, B. Cade +6 more
2022medRxiv7 citations Open access
Semantic Scholar
Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles.
J. Huffman, J. Nicolas, Julie Hahn, Adam S. Heath +132 more
2023medRxiv6 citations Open access
Semantic Scholar
cellSTAAR: Incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of non-coding regions
Eric Van Buren, Yi Zhang, Xi-Hao Li, M. Selvaraj +61 more
2025bioRxiv5 citations Open access
Semantic Scholar
Polygenic scores for obstructive sleep apnoea reveal pathways contributing to cardiovascular disease
N. Kurniansyah, S. Strausz, G. Chittoor, Shreyash Gupta +31 more
2025EBioMedicine5 citations Open access
Semantic Scholar
A large-scale genome-wide study of gene-sleep duration interactions for blood pressure in 811,405 individuals from diverse populations
P. Nagarajan, T. Winkler, Amy R. Bentley, Clint L. Miller +158 more
2025Molecular Psychiatry5 citations Open access
Semantic Scholar
Whole genome sequence analysis of apparent treatment resistant hypertension status in participants from the Trans-Omics for Precision Medicine program
N. Armstrong, V. Srinivasasainagendra, Farah Ammous, T. Assimes +40 more
2023Frontiers in Genetics5 citations Open access
Semantic Scholar
Heritability and Genetic Correlations for Sleep Apnea, Insomnia, and Hypersomnia in a Large Clinical Biobank
B. Cade, S. Redline
2023Sleep Health5 citations Open access
Semantic Scholar
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Xi-Hao Li, Han Chen, M. Selvaraj, Eric Van Buren +64 more
2023bioRxiv5 citations Open access
Semantic Scholar
Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea.
Jing-Jing Liang, He-Ming Wang, B. Cade, N. Kurniansyah +31 more
2022American Journal of Respiratory and Critical Care Medicine5 citations Open access
Semantic Scholar
Big Data Approaches for Novel Mechanistic Insights on Sleep and Circadian Rhythms: a Workshop Summary.
L. Baizer, R. Bures, Girish N. Nadkarni, Carolyn Reyes-Guzman +22 more
2025Sleep4 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

S. Redline×30
Invite
S. Redline — researcher profile on SciRah
J. Brody×29
Invite
J. Brody — researcher profile on SciRah
C. Kooperberg×26
Invite
C. Kooperberg — researcher profile on SciRah
Jennifer A. Smith×24
Invite
Jennifer A. Smith — researcher profile on SciRah

×24

Invite

Y. Chen — researcher profile on SciRah

Invite

M. Fornage — researcher profile on SciRah

Invite

P. Peyser — researcher profile on SciRah

Invite

L. Yanek — researcher profile on SciRah

Invite

S. Kardia — researcher profile on SciRah

Invite

J. Rotter — researcher profile on SciRah

Xiu-Qing Guo×19

Invite

Xiu-Qing Guo — researcher profile on SciRah

Invite

M. Irvin — researcher profile on SciRah