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Profil bibliographique

Kum Hei Ryu

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

73Publications signalées
1422Citations signalées
2Affiliations récentes

Les institutions déclarées

Les domaines associés

Helicobacter pylori-related gastroenterology studiesColorectal Cancer Screening and DetectionGastroesophageal reflux and treatmentsBRCA gene mutations in cancerGenetic factors in colorectal cancer

Les publications récentes

Accès ouvert 2026 article OpenAlex

Information-seeking experiences during genetic testing and counseling: a qualitative study of patients at high risk for hereditary breast cancer

Sun Young Park, Yeon-Joo Kim, Heejung Chae, Yoon‐Jung Choi et autres

BACKGROUND: Genetic testing and counseling have become increasingly prevalent in breast cancer treatment with the advancement of precision oncology. Understanding patients' information-seeking experiences is essential for providing better genetic cancer services. However, these experiences are insufficiently understood. This qualitative study explored the …

kr, us (code pays fourni par la source)

0 citations BMC Cancer
2026 article OpenAlex

“Every Resident Is a Doctor” : North Korea’s Word-of-Mouth-Based Therapeutic Networks and Post-Defection Medical Vertigo

Kwanwook Kim, Kum Hei Ryu, Sang Hoon Lee, Yeol Kim

본 연구는 북한의 보건의료 체계 마비 이후 기층 주민들이 국가 제도를 우회하여 대안적 의료 지식을 형성 및 실천해 온 과정을 분석했다. 면담참여자 10명의 구술 데이터에 나타난 자가 치유 실천은 비공식 경로인 ‘입소문’에서 시작되어 개별 신체의 경험적 확인을 거쳐 체화된 암묵지의 성격을 띠고 …

0 citations The Journal of the Humanities for Unification
Accès ouvert 2025 article OpenAlex

Perceptions and Readiness for Generative Artificial Intelligence Implementation Among Oncology Nurses: A Qualitative Study in a Specialized Cancer Hospital

Ji-Young Han, Kum Hei Ryu, Kwangsoo Shin

PURPOSE: In order to bridge the gap between rapid technological changes and the healthcare environment, and to alleviate the burden of nursing tasks, the need for change management must be recognized. Understanding nurses' perceptions of generative artificial intelligence (AI) is essential for …

kr, us (code pays fourni par la source)

1 citation Asian Nursing Research
Accès ouvert 2025 article OpenAlex

Comprehensive Review of Peutz–Jeghers Syndrome: Genetics, Clinical Manifestations, and Management Strategies

Jun-Kyu Kim, Eun‐Gyeong Lee, Sung Chan Park, Myong Cheol Lim et autres

Jun-Kyu Kim, R.N., Eun-Gyeong Lee, M.D., Sung Chan Park, M.D., Myong Cheol Lim, M.D., Hyeji Kim, B.S., Kum Hei Ryu, M.D., Sun-Young Kong, M.D.. Lab Med Online 2025;15:277-85. https://doi.org/10.47429/lmo.2025.15.4.277

kr (code pays fourni par la source)

0 citations Laboratory Medicine Online
Accès ouvert 2024 article OpenAlex

Acceptance of Digital Health Care Technology and the Role of Nursing Education

Ji-Young Han, Meeyoung Kim, Kum Hei Ryu, Kwangsoo Shin

Background As digital health care technology develops, the use of technology in the nursing field has become an essential part of nursing education. However, few studies have linked nurses' awareness of digital health care with nursing education. This study examines the direct …

kr (code pays fourni par la source)

1 citation The Journal of Continuing Education in Nursing
Accès ouvert 2024 article OpenAlex

Impact of graphical display on the intention to undergo risk-reducing salpingo-oophorectomy and mastectomy in individuals positive for BRCA pathogenic variant

Yoon-Jung Choi, Younju Park, Boyoung Park, Heejung Chae et autres

The BRCA1/2 pathogenic variant (PV) increases the risk of breast and ovarian cancer; thus, risk-reducing salpingo-oophorectomy (RRSO) and mastectomy (RRM) are recommended. We evaluated the effects of the graphical display of cancer risk compared with those of numerical presentation on the decision-making …

kr, us (code pays fourni par la source)

1 citation Scientific Reports
Accès ouvert 2024 article OpenAlex

Clinical Significance of PALB2 Pathogenic Germline Variant

Minchae Kang, Richards Sashika N., Jong Eun Park, Mi‐Ae Jang et autres

Min-Chae Kang, R.N., Jong Eun Park, M.D., Mi-Ae Jang, M.D., Dongju Won, M.D., Boyoung Park, M.D., Seeyoun Lee, M.D., Dong Ock Lee, M.D., Kum Hei Ryu, M.D., Yoon-Jung Chang, M.D., Sun-Young Kong, M.D.. Lab Med Online 2024;14:311-20. https://doi.org/10.47429/lmo.2024.14.4.311

us, kr (code pays fourni par la source)

0 citations Laboratory Medicine Online
Accès ouvert 2024 review OpenAlex

Healthcare Professionals’ Learning Needs and Perspectives on Essential Information in Genetic Cancer Care: A Systematic Review

Sun Young Park, Youlim Kim, Maria C. Katapodi, Yeon-Joo Kim et autres

BACKGROUND: The increased demand for genetic testing and counseling necessitates healthcare professionals (HCPs) to improve their genetic competency through training programs. This systematic review identified HCPs' learning needs and their perspectives on essential information for families with hereditary cancer. METHODS: This review …

kr, ch (code pays fourni par la source)

7 citations Cancers
2024 conference-abstract OpenAlex

Abstract 7332: Healthcare professionals' perceptions and educational needs in genetic counseling for cancer risk management: An integrated mixed-methods systematic review

So‐Youn Jung, Sun Young Park, Eun‐Gyeong Lee, Heejung Chae et autres

Abstract Background: The role of healthcare professionals (HCPs) is crucial in the genetic counseling process for managing hereditary cancer risks. However, HCPs face challenges due to a lack of specialized training and confidence, particularly in communicating genetic risks to patients. Hence, it …

kr (code pays fourni par la source)

1 citation Cancer Research
2024 conference-abstract OpenAlex

Abstract 7336: Exploring the impact of cancer predisposition gene variants by functional analysis and whole genome sequencing analysis in hereditary cancer patients

Hyeji Kim, Jong Eun Park, Gi Yeon Lee, Jung-Ah Hwang et autres

Abstract Background: Hereditary cancer confirmed by germline pathogenic variant has been increased with increasing next generation sequencing (NGS) panel tests in recent years. However, some cases who were suspected hereditary cancer represented having variant of uncertain significance (VUS) or no variants even …

kr (code pays fourni par la source)

0 citations Cancer Research

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