Michael W. Pauciulo - Concepedia

Author

Michael W. Pauciulo

Cincinnati Children's Hospital Medical Center ORCID

Also Known As

Diane K Kissell, M. Pauciulo, M. W. Pauciulo, M.W. Pauciulo, Michael Pauciulo, Michael W Pauciulo, Michael W. Pauciulo, Michael W. Pauciulo, Pauciulo, Michael, Pauciulo, Michael W

130

Publications

6.6K

Citations

H-Index

Concepts

All Affiliations

Cincinnati Children's Hospital Medical Center University of Cincinnati University of Cincinnati Medical Center University of Colorado Denver Columbia University Irving Medical Center

About

Michael W. Pauciulo is an author at Cincinnati Children's Hospital Medical Center specializing in medicine, public health, and pulmonary vascular disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	19	2.6K
2	Public Health	14	15	2.4K
3	African American Studies	1	1	54
4	Allergy	1	1	32
5	Biostatistics	1	1	11

Michael W. Pauciulo

Publications

6.2K

Citations

H-Index

Page 1

	Year	Citations
Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension Kirk B. Lane, Rajiv D. Machado, Michael W. Pauciulo, Nature Genetics HypertensionPulmonary Arterial HypertensionTgf-β ReceptorGenetic DisorderGenetics	2000	1.5K
Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia Richard C. Trembath, Jennifer R. Thomson, Rajiv D. Machado, New England Journal of Medicine	2001	719
BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension Rajiv D. Machado, Michael W. Pauciulo, Jennifer R. Thomson, The American Journal of Human Genetics HypertensionPulmonary Arterial HypertensionPulmonary CirculationPrimary Pulmonary HypertensionInherited Molecular Mechanism	2001	533
Glucocerebrosidase activity in Parkinson’s disease with and without<i>GBA</i>mutations Roy N. Alcalay, Oren Levy, Cheryl Waters, Brain	2015	389
Comparison of Parkinson Risk in Ashkenazi Jewish Patients With Gaucher Disease and<i>GBA</i>Heterozygotes Roy N. Alcalay, Tama Dinur, Timothy J. Quinn, JAMA Neurology	2014	211
High Frequency of <i>BMPR2</i> Exonic Deletions/Duplications in Familial Pulmonary Arterial Hypertension Joy D. Cogan, Michael W. Pauciulo, Amy P. Batchman, American Journal of Respiratory and Critical Care Medicine	2006	210
Mutations in <i>GBA</i> are associated with familial Parkinson disease susceptibility and age at onset William C. Nichols, Nathan Pankratz, D. K. Marek, Neurology	2008	194
Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease Na Zhu, Carrie L. Welch, Jiayao Wang, Genome Medicine	2018	153
Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With Adults Na Zhu, Claudia Gonzaga‐Jauregui, Carrie L. Welch, Circulation Genomic and Precision Medicine	2018	148
Parkinson disease phenotype in Ashkenazi jews with and without <i>LRRK2</i> G2019S mutations Roy N. Alcalay, Anat Mirelman, Rachel Saunders‐Pullman, Movement Disorders	2013	142

Page 1