Rebecca Reimers

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Title(s)	Assistant Clinical Professor, Pediatrics
School	Vc-health Sciences-schools
Address	9500 Gilman Drive # La Jolla CA 92093
vCard	Download vCard

Bibliographic

publications

Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.

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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.

Novel Therapeutic Treatments in Perinatal Genetics Bridging Prenatal and Postnatal Care of Genetic Conditions. Clin Ther. 2026 Jul; 48(7):555-556. Russo ML, Reimers R, Talati AN. PMID: 42264972.

View in: PubMed Mentions: Fields:
Dru Drug Therapy The Therapeutics
The Fastest NICU Genome is One Completed (or at Least Coordinated) Prenatally: A Joint Perspective From United States-Based Maternal-Fetal Medicine and Neonatologist-Geneticists. Clin Ther. 2026 Jul; 48(7):588-591. Reimers R, Chaudhari BP. PMID: 42209309.

View in: PubMed Mentions: Fields:
Dru Drug Therapy The Therapeutics
Translation:Humans
Clinical utility and cost-effectiveness of BeginNGS newborn screening by genome sequencing and standard newborn screening for severe childhood genetic diseases: an adaptive, international and comparative clinical trial. BMJ Open. 2025 Nov 13; 15(11):e098609. Reimers R, Bailey M, Brown C, Chan K, Defay T, Finkel T, Kahn S, Protopsaltis L, Stoddard L, Talati AJ, Wigby K, Wigby K, Akil ASA, Wright M, Kingsmore SF, BeginNGS Consortium. PMID: 41238356; PMCID: PMC12625857.

View in: PubMed Mentions: 2 Fields:
Med Medicine (General)
Translation:Humans PHPublic Health
Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations. Nat Commun. 2025 Aug 07; 16(1):7267. Kobren SN, Moldovan MA, Reimers R, Traviglia D, Li X, Barnum D, Veit A, Corona RI, Carvalho Neto GV, Willett J, Berselli M, Ronchetti W, Nelson SF, Martinez-Agosto JA, Sherwood R, Krier J, Kohane IS, Undiagnosed Diseases Network, Sunyaev SR. PMID: 40770127; PMCID: PMC12328722.

View in: PubMed Mentions: 1 Fields:
Bio Biology Sci Science
Translation:Humans
Advancing precision care in pregnancy through a treatable fetal findings list. Am J Hum Genet. 2025 06 05; 112(6):1251-1269. Cohen JL, Duyzend M, Adelson SM, Yeo J, Fleming M, Ganetzky R, Hale R, Mitchell DM, Morton SU, Reimers R, Roberts A, Strong A, Tan W, Thiagarajah JR, Walker MA, Green RC, Gold NB. PMID: 40209713; PMCID: PMC12256799.

View in: PubMed Mentions: 2 Fields:
Gen Genetics
Translation:Humans
A machine learning decision support tool optimizes WGS utilization in a neonatal intensive care unit. NPJ Digit Med. 2025 Jan 30; 8(1):72. Juarez EF, Peterson B, Sanford Kobayashi E, Gilmer S, Tobin LE, Schultz B, Lenberg J, Carroll J, Bai-Tong S, Sweeney NM, Beebe C, Stewart L, Olsen L, Reinke J, Kiernan EA, Reimers R, Wigby K, Tackaberry C, Yandell M, Hobbs C, Bainbridge MN. PMID: 39885315; PMCID: PMC11782664.

View in: PubMed Mentions: 1
Prequalification of genome-based newborn screening for severe childhood genetic diseases through federated training based on purifying hyperselection. Am J Hum Genet. 2024 12 05; 111(12):2618-2642. Kingsmore SF, Wright M, Smith LD, Liang Y, Mowrey WR, Protopsaltis L, Bainbridge M, Baker M, Batalov S, Blincow E, Cao B, Caylor S, Chambers C, Ellsworth K, Feigenbaum A, Frise E, Guidugli L, Hall KP, Hansen C, Kiel M, Van Der Kraan L, Krilow C, Kwon H, Madhavrao L, Lefebvre S, Leipzig J, Mardach R, Moore B, Oh D, Olsen L, Ontiveros E, Owen MJ, Reimers R, Scharer G, Schleit J, Shelnutt S, Mehtalia SS, Oriol A, Sanford E, Schwartz S, Wigby K, Wigby K, Willis MJ, Yandell M, Kunard CM, Defay T. PMID: 39642867; PMCID: PMC11639087.

View in: PubMed Mentions: 5 Fields:
Gen Genetics
Translation:Humans PHPublic Health
Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial. Am J Hum Genet. 2024 12 05; 111(12):2643-2667. Kingsmore SF, Wright M, Olsen L, Schultz B, Protopsaltis L, Averbuj D, Blincow E, Carroll J, Caylor S, Defay T, Ellsworth K, Feigenbaum A, Gover M, Guidugli L, Hansen C, Van Der Kraan L, Kunard CM, Kwon H, Madhavrao L, Leipzig J, Liang Y, Mardach R, Mowrey WR, Nguyen H, Niemi AK, Oh D, Saad M, Scharer G, Schleit J, Mehtalia SS, Sanford E, Smith LD, Willis MJ, Wigby K, Wigby K, Reimers R. PMID: 39642868; PMCID: PMC11639094.

View in: PubMed Mentions: 8 Fields:
Gen Genetics
Translation:Humans PHPublic Health
Prenatal Ultrasonographic Features Associated With ARSL and X-Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series. Prenat Diagn. 2024 12; 44(13):1663-1670. Broeren E, Stover S, Bennett K, Giordano J, Galloway S, Lauzon J, Rust L, Suerink M, van Haeringen A, Australian Genomic Autopsy Study Team, Reimers R. PMID: 39313411.

View in: PubMed Mentions: Fields:
Obs Obstetrics
Translation:Humans
Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations. bioRxiv. 2024 Aug 13. Kobren SN, Moldovan MA, Reimers R, Traviglia D, Li X, Barnum D, Veit A, Corona RI, Carvalho Neto GV, Willett J, Berselli M, Ronchetti W, Nelson SF, Martinez-Agosto JA, Sherwood R, Krier J, Kohane IS, Undiagnosed Diseases Network, Sunyaev SR. PMID: 38405764; PMCID: PMC10888768.

View in: PubMed Mentions:
A Machine Learning Decision Support Tool Optimizes Whole Genome Sequencing Utilization in a Neonatal Intensive Care Unit. medRxiv. 2024 Jul 07. Juarez EF, Peterson B, Kobayashi ES, Gilmer S, Tobin LE, Schultz B, Lenberg J, Carroll J, Bai-Tong S, Sweeney NM, Beebe C, Stewart L, Olsen L, Reinke J, Kiernan EA, Reimers R, Wigby K, Tackaberry C, Yandell M, Hobbs C, Bainbridge MN. PMID: 39006422; PMCID: PMC11245077.

View in: PubMed Mentions:
Unique Challenges of NIPT for Sex Chromosome Aneuploidy. Clin Obstet Gynecol. 2023 09 01; 66(3):568-578. Wilkins-Haug L, Reimers R. PMID: 37650669; PMCID: PMC10491423.

View in: PubMed Mentions: 4 Fields:
Gyn Gynecology Obs Obstetrics
Translation:Humans Cells
Position statement from the International Society for Prenatal Diagnosis on the use of non-invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies. Prenat Diagn. 2023 06; 43(7):814-828. Hui L, Ellis K, Mayen D, Pertile MD, Reimers R, Sun L, Vermeesch J, Vora NL, Chitty LS. PMID: 37076973.

View in: PubMed Mentions: 39 Fields:
Obs Obstetrics
Translation:Humans
Validation of claims-based algorithms to identify non-live birth outcomes. Pharmacoepidemiol Drug Saf. 2023 04; 32(4):468-474. Zhu Y, Bateman BT, Hernandez-Diaz S, Gray KJ, Straub L, Reimers RM, Manning-Geist B, Yoselevsky E, Taylor LG, Ouellet-Hellstrom R, Ma Y, Qiang Y, Hua W, Huybrechts KF. PMID: 36420643; PMCID: PMC10906136.

View in: PubMed Mentions: 8 Fields:
Dru Drug Therapy Epi Epidemiology
Translation:Humans
Genetic diagnosis in the fetus. J Perinatol. 2020 07; 40(7):997-1006. Wojcik MH, Reimers R, Poorvu T, Agrawal PB. PMID: 32094481; PMCID: PMC7319864.

View in: PubMed Mentions: 7 Fields:
Per Perinatology
Translation:Humans