J. Malinowski

发表

Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis

Manuel A. R. Ferreira, James R. Staley, Daniel F. Freitag, 2015, The lancet. Diabetes & endocrinology.

Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

David T. Miller, L. Demmer, M. Scheuner, 2020, Genetics in Medicine.

Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci

Gerard Tromp, Marylyn D. Ritchie, Dana C. Crawford, 2017, Circulation research.

The genetic underpinnings of variation in ages at menarche and natural menopause among women from the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) Study: A trans-ethnic meta-analysis

Janina M. Jeff, E. Demerath, C. Carty, 2018, PloS one.

Robert J. Goodloe, D. Crawford, K. Brown-Gentry, 2015, Front. Genet..

Alpha Blocker Versus Calcium Channel Blocker for Pheochromocytoma

G. Callender, J. Malinowski, E. Holt, 2018 .

Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network

Suzette J. Bielinski, Christopher G. Chute, Marylyn D. Ritchie, 2014, PloS one.

Genetic testing for the epilepsies: A systematic review

A. Poduri, D. Gloss, L. Bier, 2021, Epilepsia.

Observational study of population genomic screening for variants associated with endocrine tumor syndromes in a large, healthcare-based cohort

A. Sturm, A. Buchanan, M. Kelly, 2022, BMC Medicine.

Intellectual property considerations for molecular diagnostic development with emphasis on companion diagnostics

J. Malinowski, R. Warburg, Harry Glorikian, 2018, Expert opinion on therapeutic patents.

The uptake and utility of genetic testing and genetic counseling for hypertrophic cardiomyopathy—A systematic review and meta‐analysis

J. Natoli, A. Cirino, M. Kelly, 2022, Journal of genetic counseling.

Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study.

Robert J. Goodloe, C. Carlson, M. Fornage, 2013, Human reproduction.

Genetic Variation and Reproductive Timing: African American Women from the Population Architecture Using Genomics and Epidemiology (PAGE) Study

C. Carlson, C. Carty, T. Matise, 2013, PloS one.

Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability

David T. Miller, L. Demmer, M. Scheuner, 2020, Genetics in Medicine.

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

Cue Hyunkyu Lee, M. Fornage, A. Hofman, 2018, Journal of the American Heart Association.

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

Cue Hyunkyu Lee, Gao T. Wang, Benjamin J. Wright, 2016, Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease.

Vasopressor choice for hypotension in elective Cesarean section: ephedrine or phenylephrine?

J. Malinowski, Sathees B. C. Chandra, Venkatesh G. Suryanarayana, 2010, Archives of medical science : AMS.

Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)

Danny E Miller, T. Yu, H. Kearney, 2021, Genetics in Medicine.

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).

Y. Akkari, K. Monaghan, J. Malinowski, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Parathyroidectomy prior to kidney transplant decreases graft failure

M. Javid, S. Kulkarni, T. Carling, 2017, Surgery.

Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia.

Harvey Risch, Peter Kraft, Dana C Crawford, 2014, Carcinogenesis.

Diagnostic validity and clinical utility of genetic testing for hypertrophic cardiomyopathy: a systematic review and meta-analysis

J. Natoli, M. Kelly, J. Malinowski, 2022, Open Heart.

Identifying Heart Failure from Electronic Health Records: A Systematic Evidence Review

V. Roger, L. Rasmussen, S. Bielinski, 2021, medRxiv.

Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies.

Marco L. Leung, J. Malinowski, Elizabeth S. Barrie, 2022, Genetics in Medicine.

Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies.

Marco L. Leung, J. Malinowski, Elizabeth S. Barrie, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Phenylalanine hydroxylase deficiency treatment and management: A systematic evidence review of the American College of Medical Genetics and Genomics (ACMG).

P. Rothberg, J. Malinowski, April D. Adams, 2023, Genetics in medicine : official journal of the American College of Medical Genetics.

Y. Akkari, K. Monaghan, J. Malinowski, 2023, Genetics in medicine : official journal of the American College of Medical Genetics.

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

Cue Hyunkyu Lee, M. Fornage, L. Kiemeney, 2016, Journal of the American Heart Association.

Dissection of Levels II Through V Is Required for Optimal Outcomes in Patients with Lateral Neck Lymph Node Metastasis from Papillary Thyroid Carcinoma.

M. Javid, T. Carling, R. Udelsman, 2016, Journal of the American College of Surgeons.

Replication of genetic loci for ages at menarche and menopause in the multi-ethnic Population Architecture using Genomics and Epidemiology (PAGE) study.

Robert J. Goodloe, C. Carlson, M. Fornage, 2013, Human reproduction.