Teresa Kruisselbrink

机构：Helix (United States) · ORCID：0009-0002-3295-6624

发表论文 59 篇 · 总被引 1643 次 · h-index 18

代表论文

• Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome (2022 · Genome Medicine · 被引 24)
• Impact of integrated translational research on clinical exome sequencing (2023 · Genetics in Medicine · 被引 14)
• Mayo Clinic Tapestry Study (2024 · Mayo Clinic Proceedings · 被引 13)
• Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD) (2023 · Journal of Translational Medicine · 被引 12)
• An intervention strategy to improve genetic testing for dilated cardiomyopathy in a heart failure clinic (2022 · Genetics in Medicine · 被引 11)
• Rare TBX4 Variant Causing Pulmonary Arterial Hypertension With Small Patella Syndrome in an Adult Man (2021 · JACC Case Reports · 被引 6)