Jennifer Kemppainen - Mayo Clinic - Rochester

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论文共 38 篇作者统计合作学者相似作者

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P201: the Clinical Utility of Next-Generation Sequencing (Ngs)-Based Genetic Testing in Pediatric Polycystic Kidney Disease

Elif Bozkurt, Hana Yang,Jennifer Kemppainen, Tracy Baker, Mohamad Sheikh Najeeb, Whitney Thompson,Cheryl Tran, David Sas,Carl Cramer, Fouad Chebib,Neera Dahl, Vicente Torres,Filippo Pinto E Vairo, Peter Harris,Christian Hanna

Genetics in Medicine Open (2025): 102166

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Genetic Testing Goes Beyond Imaging and Histological Evaluation in Pleuroparenchymal Fibroelastosis

Ghadah Alrehaili,Jennifer Kemppainen,Sanjay Kalra,Filippo Pinto e Vairo,Teng Moua,Eunhee S. Yi,Alejandro Ferrer,Mrinal M. Patnaik,Eva M. Carmona

LUNG（2024）

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Mayo Clinic Tapestry Study: A Large-Scale Decentralized Whole Exome Sequencing Study for Clinical Practice, Research Discovery, and Genomic Education

Lorelei A. Bandel,Robert A. Vierkant,Teresa M. Kruisselbrink, Michelle L. Bublitz, Tammy A. Wilson,Sebastian M. Armasu,Jan B. Egan,Richard J. Presutti,Niloy Jewel J. Samadder, Aleksandar Sekulic,Rory J. Olson, Jennifer Tan-Arroyo, Joel A. Morales-Rosado,Eric W. Klee,Matthew J. Ferber,Jennifer L. Kemppainen,Jennifer L. Anderson, Jessa S. Bidwell, Joseph J. Wick,Victor E. Ortega,William Bobo,Pavel N. Pichurin, Jessica M. Mcmillan, DeAnna M. Weaver,Douglas L. Riegert-Johnson, Alanna M. Cera, Lauren M. Boucher,Iftikhar J. Kullo, Sarah K. Mantia, Matthew T. Jones,Nicholas B. Larson, Tony C. Luehrs, Jon W. Leitzke,Hugues Sicotte,Shulan Tian, Jennifer R. Stavlund,Joel E. Pacyna,Richard R. Sharp, Akwasi A. Asabere, James Lu,Tammy M. Mcallister, T'Nita S. Walker,A. Keith Stewart,Gianrico Farrugia,Konstantinos N. Lazaridis

MAYO CLINIC PROCEEDINGSno. 12 (2024): 1878-1894

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Implementation of Genomic Medicine for Rare Disease in a Tertiary Healthcare System: Mayo Clinic Program for Rare and Undiagnosed Diseases (Praud)

Filippo Pinto e Vairo,Jennifer L. Kemppainen,Carolyn R. Rohrer Vitek, Denise A. Whalen,Kayla J. Kolbert,Kaitlin J. Sikkink,Sarah A. Kroc,Teresa Kruisselbrink,Gabrielle F. Shupe,Alyssa K. Knudson,Elizabeth M. Burke,Elle C. Loftus,Lorelei A. Bandel,Carri A. Prochnow,Lindsay A. Mulvihill,Brittany Thomas,Dale M. Gable, Courtney B. Graddy,Giovanna G. Moreno Garzon,Idara U. Ekpoh,Eva M. Carmona Porquera,Fernando C. Fervenza,Marie C. Hogan,Mireille El Ters,Kenneth J. Warrington,John M. Davis,Matthew J. Koster,Amir B. Orandi,Matthew L. Basiaga,Adrian Vella,Seema Kumar,Ana L. Creo,Aida N. Lteif,Siobhan T. Pittock,Peter J. Tebben,Ejigayehu G. Abate,Avni Y. Joshi,Elizabeth H. Ristagno,Mrinal S. Patnaik,Lisa A. Schimmenti,Radhika Dhamija,Sonia M. Sabrowsky,Klaas J. Wierenga,Mira T. Keddis,Niloy Jewel J. Samadder,Richard J. Presutti,Steven I. Robinson,Michael C. Stephens,Lewis R. Roberts,William A. Faubion,Sherilyn W. Driscoll,Lily C. Wong-Kisiel,Duygu Selcen,Eoin P. Flanagan,Vijay K. Ramanan,Lauren M. Jackson,Michelle L. Mauermann,Victor E. Ortega,Sarah A. Anderson,Stacy L. Aoudia,Eric W. Klee,Tammy M. McAllister,Konstantinos N. Lazaridis

Journal of Translational Medicine（2024）

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Exome Sequencing Identifies Carriers of the Autosomal Dominant Cancer Predisposition Disorders Beyond Current Practice Guideline Recommendations

N. Jewel Samadder, Emily Gay, Vanda Lindpere, Michelle L. Bublitz,Lorelei A. Bandel,Sebastian M. Armasu,Robert A. Vierkant,Matthew J. Ferber,Eric W. Klee,Nicholas B. Larson,Teresa M. Kruisselbrink,Jan B. Egan,Jennifer L. Kemppainen, Jessa S. Bidwell,Jennifer L. Anderson,Tammy M. McAllister, T'Nita S. Walker,Katie L. Kunze,Michael A. Golafshar,Margaret A. Klint,Richard J. Presutti,William V. Bobo,Aleksander Sekulic, Jolene M. Summer-Bolster,Cheryl L. Willman,Konstantinos N. Lazaridis

JCO Precision Oncology (2024)

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Mayo Clinic Tapestry Study

Lorelei A. Bandel,Robert A. Vierkant,Teresa M. Kruisselbrink, Michelle L. Bublitz, Tammy A. Wilson,Sebastian M. Armasu,Jan B. Egan,Richard J. Presutti,Niloy Jewel J. Samadder, Aleksandar Sekulic,Rory J. Olson, Jennifer Tan-Arroyo, Joel A. Morales-Rosado,Eric W. Klee,Matthew J. Ferber,Jennifer L. Kemppainen,Jennifer L. Anderson, Jessa S. Bidwell, Joseph J. Wick,Victor E. Ortega,William V. Bobo,Pavel N. Pichurin, Jessica M. Mcmillan, DeAnna M. Weaver,Douglas L. Riegert-Johnson, Alanna M. Cera, Lauren M. Boucher,Iftikhar J. Kullo, Sarah K. Mantia, Matthew T. Jones,Nicholas B. Larson, Tony C. Luehrs, Jon W. Leitzke,Hugues Sicotte,Shulan Tian, Jennifer R. Stavlund,Joel E. Pacyna,Richard R. Sharp, Akwasi A. Asabere, James Lu,Tammy M. McAllister, T’Nita S. Walker,A. Keith Stewart,Gianrico Farrugia,Konstantinos N. Lazaridis

Mayo Clinic Proceedingsno. 12 (2024): 1878-1894

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EMBEDDING GENOME SEQUENCING AND GENETIC COUNSELLING INTO THE MALE INFERTILITY PRACTICE

Christopher J. Warren, Kaitlin Sikkink Brown, Kayla Kolbert,Laura Duncan,Sarah Kroc, Emily Toering, Chloe Gill, Sonia Sabrowsky, Alyssa Knudson,Jennifer Kemppainen,Filippo Pinto E. Vairo,Jewel Samadder,Sevann Helo,Nahid Punjani

FERTILITY AND STERILITY（2024）

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Diagnostic Yield of Exome and Genome Sequencing after Non-Diagnostic Multi-Gene Panels in Patients with Single-System Diseases

Matheus V. M. B. Wilke,Eric W. Klee,Radhika Dhamija,Fernando C. Fervenza,Brittany Thomas,Nelson Leung,Marie C. Hogan,Megan M. Hager,Kayla J. Kolbert,Jennifer L. Kemppainen,Elle C. Loftus, Katie M. Leitzen,Carolyn R. Vitek,Tammy McAllister,Konstantinos N. Lazaridis,Filippo Pinto e Vairo

Orphanet Journal of Rare Diseasesno. 1 (2024)

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Role of Genetic Testing in Pleuroparenchymal Fibroelastosis

Joelle Friesen, Ghadah Alrehaili,Jennifer Kemppainen,Sanjay Kalra, Filippo Pinto Vairo,Teng Moua,Eunhee Yi,Alejandro Ferrer,Mrinal Patnaik,Eva Carmona

EUROPEAN RESPIRATORY JOURNAL (2024)

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65 Gene-specific Risk of Syndrome-Associated Cancers in First-Degree Relatives of Pancreatic Cancer Patients with Pathogenic/likely Pathogenic Variants

Xuan Chen,Kari G. Rabe,Margaret A. Meyer,Jennifer L. Kemppainen,Masayasu Horibe,Shruti Chandra,Shounak Majumder,Gloria M. Petersen

Journal of Clinical and Translational Scienceno. s1 (2023): 18-18

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