Ulrike Schwarze

Seattle Pacific University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

36h-index9.0kcitations90works3.82yr avg
OpenAlex↗Google Scholar↗Lab page↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Connective tissue disorders research(62), Cell Adhesion Molecules Research(11), Bone and Dental Protein Studies(11), Aortic Disease and Treatment Approaches(8), Aortic aneurysm repair treatments(8)

Publications90 total

A comprehensive multidisciplinary thoracic aortic program improves patient quality metrics after type A aortic dissection repair
JTCVS Open·2025Open Access
Institutional impact of multidisciplinary aortic team implementation on practice patterns and surgical productivity
Seminars in Vascular Surgery·2025
Incidence and Description of Confirmed Genetic Mutations Among Patients With Aortic Pathology
Journal of Vascular Surgery·2025Open Access
Non-canonical splice variants in thoracic aortic dissection cases and Marfan syndrome with negative genetic testing
npj Genomic Medicine·2025Open Access
Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition
Nature Genetics·2025· 27 citedOpen Access
Multidisciplinary hybrid approach to management of a thoracoabdominal aneurysm in a patient with both Loeys-Dietz and vascular Ehlers-Danlos syndrome
Journal of Vascular Surgery Cases and Innovative Techniques·2024· 1 citedOpen Access
Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts
Rare·2024· 2 citedOpen Access
P210: Unexpected recurrence of vascular Ehlers-Danlos syndrome in sibships due to parental mosaicism for COL3A1 variants
Genetics in Medicine Open·2024Open Access
Synchronized long-read genome, methylome, epigenome, and transcriptome for resolving a Mendelian condition
2023· 7 citedOpen Access
Full-length Isoform Sequencing for Resolving the Molecular Basis of Charcot-Marie-Tooth 2A
Neurology Genetics·2023· 6 citedOpen Access
Dominant‐negative variant in <i>SLC1A4</i> causes an autosomal dominant epilepsy syndrome
Annals of Clinical and Translational Neurology·2023· 3 citedOpen Access
Splenic artery pathology presentation, operative interventions, and outcomes in 88 patients with vascular Ehlers-Danlos syndrome
Journal of Vascular Surgery·2023· 7 citedOpen Access
Full-length isoform sequencing for resolving the molecular basis of Charcot-Marie-Tooth 2A
2023Open Access
EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis
The American Journal of Human Genetics·2022· 21 citedOpen Access
Marfan syndrome resulting from a rare pathogenic <scp><i>FBN1</i></scp> variant, ascertained through a proband with <scp>IgG4</scp>‐related arteriopathy
American Journal of Medical Genetics Part A·2021Open Access
Abnormal Bone Collagen Cross‐Linking in Osteogenesis Imperfecta/Bruck Syndrome Caused by Compound Heterozygous <scp><i>PLOD2</i></scp> Mutations
JBMR Plus·2020· 28 citedOpen Access
Multicenter Clinicopathologic Correlation of Kidney Biopsies Performed in COVID-19 Patients Presenting With Acute Kidney Injury or Proteinuria
American Journal of Kidney Diseases·2020· 184 citedOpen Access
A family with Classical Ehlers-Danlos Syndrome (cEDS), mild bone fragility and without vascular complications, caused by the p.Arg312Cys mutation in COL1A1
European Journal of Medical Genetics·2019· 14 cited
Compound heterozygosity for a frameshift mutation and an upstream deletion that reduces expression of <i>SERPINH1</i> in siblings with a moderate form of osteogenesis imperfecta
American Journal of Medical Genetics Part A·2019· 8 cited
A novel Ser40Trp variant in IFITM5 in a family with osteogenesis imperfecta and review of the literature
Clinical Dysmorphology·2019· 16 cited
page 1 of 5Next →

Frequent Co-authors

Peter H. Byers(39), Melanie Pepin(12), David R. Eyre(6), James M. Pace(4), David W. Russell(4), Tobias Sommer(4), Sofie Symoens(3), Andrea Superti‐Furga(3), Daniel H. Cohn(3), Deborah Krakow(3), Diana Chen(3), Kathleen Yang(3), Elizabeth M. Petty(3), Shawna M. Pyott(3), Dru F. Leistritz(3), MaryAnn Weis(3), Andreas Winterpacht(3), Stefan Mundlos(3), Lynne T. Smith(3), Bert Callewaert(2)