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William C. Nichols | Researchclopedia

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William C. Nichols

Cincinnati Children's Hospital Medical Center ORCID

298

Works

18,937

Citations

65

h-index

166

i10-index

Research Topics

Pulmonary Hypertension Research and Treatments Parkinson's Disease Mechanisms and Treatments Lysosomal Storage Disorders Research

Affiliations

Florida State University1975–1975

Northwestern University2004–2007

University of Geneva1999–1999

Cedars-Sinai Medical Center2014–2014

Cincinnati Children's Hospital Medical Center1999–2025

Top Works

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

Gallia G. Levy,William C. Nichols,et al.

20011,742 citations

Counseling, Therapy, and Family Dynamics

Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis

Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Kirk B. Lane,Rajiv D. Machado,et al.

20001,481 citations

Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia

Richard C. Trembath,Jennifer R. Thomson,et al.

2001720 citations

BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary Hypertension

Rajiv D. Machado,Michael W. Pauciulo,et al.

2001536 citations

Introduction to the Work of Melanie Klein

William C. Nichols,Hanna Segal,et al.

1976496 citations

The Language of Psycho-Analysis

William C. Nichols,E. Laplanche,et al.

1976494 citations

Mutations in the ER–Golgi Intermediate Compartment Protein ERGIC-53 Cause Combined Deficiency of Coagulation Factors V and VIII

William C. Nichols,Uri Seligsohn,et al.

1998463 citations

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

William C. Nichols,Nathan Pankratz,et al.

2005453 citations

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Nathan Pankratz,Jemma B. Wilk,et al.

2008443 citations