Expanding Genetic Counselor Roles: A Model for Global Research Development.

genetic counselors publications research

Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
01 Jul 2024
Historique:
received: 09 05 2024
revised: 07 06 2024
accepted: 22 06 2024
medline: 27 7 2024
pubmed: 27 7 2024
entrez: 27 7 2024
Statut: epublish

Résumé

Genetic counselors (GCs) increasingly play key roles in advancing genomic medicine through innovative research. Here, we examine one large cohort of GCs' evolving contributions to the literature, with the goal of facilitating worldwide professional development for GCs through scholarly activities. Publications were cataloged by members of the Section of Genetic Counseling (Section), established at the Children's Hospital of Philadelphia and the University of Pennsylvania in 2014, including publication year, journal, impact factor, and author position. Data were organized using the "My Bibliography" tool on the National Center for Biotechnology Information website and a Research Electronic Data Capture database created to initially collect manuscripts published through 30 June 2020. A subsequent survey captured publications through 5 February 2024. An amount of 52 of 120 (43%) GCs shared their curriculum vitae/papers. 992 unique publications were identified from 1986 to 2024. Since 2013, no less than 32 papers were published annually by Section members and no less than 10 GCs contributed to publications yearly. Impact factors typically averaged >5.0 per year. Areas of foci diversified considerably since 2015. Here, we establish that GCs indeed contribute to scholarly work as evidenced by the number of publications alone. The establishment of an academic home may have contributed, given publications increased concurrent to launching the Section, providing a model for organizing GCs at institutions nationally and internationally. Highlighting such achievements will foster the expansion of GC roles in the era of precision genomic medicine and therapy. Considering ways to support GCs towards expanding these activities is equally important.

Identifiants

pubmed: 39062646
pii: genes15070867
doi: 10.3390/genes15070867
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Colleen C Muraresku (CC)

Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Elizabeth M McCormick (EM)

Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Lydia Rockart (L)

22q and You Center, Clinical Genetics, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

T Blaine Crowley (T)

22q and You Center, Clinical Genetics, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Stephanie Asher (S)

Division of Translational Medicine and Human Genetics, Department of Medicine, Perelman School of Medicine, Penn Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Amanda Back (A)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Neurology, The Epilepsy Neurogenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Sarah M Baldino (SM)

Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Emma Bedoukian (E)

Roberts Individualized Medical Genetics Center (RIMGC), Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Allison D Britt (AD)

Comprehensive Vascular Anomalies Program, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Natalie Burrill (N)

Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Cara Cacioppo (C)

Penn Telegenetics Program, University of Pennsylvania, Philadelphia, PA 19104, USA.

Dana Farengo Clark (DF)

Division of Hematology and Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Mary Egan Clark (ME)

Division of Hematology and Oncology, Department of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Laura Conway (L)

Master of Science in Genetic Counseling Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Laynie Dratch (L)

Department of Neurology, University of Pennsylvania, Philadelphia, PA 19104, USA.

Holly A Dubbs (HA)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Nicole M Engelhardt (NM)

Section of Biochemical Genetics, Division of Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Natalie Ginn (N)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Neurology, The Epilepsy Neurogenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Christopher Gray (C)

Roberts Individualized Medical Genetics Center (RIMGC), Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Tiff Hartman (T)

Master of Science in Genetic Counseling Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Evan R Hathaway (ER)

Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Katherine L Helbig (KL)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Lily Hoffman-Andrews (L)

Division of Cardiovascular Medicine, Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Stefanie Kasperski (S)

Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Beth A Keena (BA)

Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Kierstin N Keller (KN)

Center for Mitochondrial and Epigenomic Medicine, Department of Pathology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Jessica M Long (JM)

Basser Center for BRCA, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Lauren Lulis (L)

Division of Genomic Diagnostics, Department of Pathology, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Laina Lusk (L)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Neurology, The Epilepsy Neurogenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Daniel E McGinn (DE)

Mitochondrial Medicine Frontier Program, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
22q and You Center, Clinical Genetics, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Rebecca Mueller (R)

Masters Genetic Counseling Program, Department of Medical Ethics and Health Policy, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Rache A Paul (RA)

Department of Neurology, University of Pennsylvania, Philadelphia, PA 19104, USA.

Lisa Pilchman (L)

Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Jacquelyn Powers (J)

Basser Center for BRCA, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Sarah E Raible (SE)

Roberts Individualized Medical Genetics Center (RIMGC), Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Sara Reichert (S)

Division of Genomic Diagnostics, Department of Pathology, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Alyssa L Rippert (AL)

Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Angela G Arnold (AG)

Basser Center for BRCA, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Sarah M Ruggiero (SM)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Neurology, The Epilepsy Neurogenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Neurology, The Epilepsy Neurogenetics Initiative, Center for Epilepsy and Neurodevelopmental Disorders (ENDD), Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Erica Schindewolf (E)

CHOP Precision Medicine Services, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Katie Rose Sullivan (KR)

Division of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Division of Neurology, The Epilepsy Neurogenetics Initiative, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Shannon Terek (S)

Center for Applied Genomics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Bekah Wang (B)

22q and You Center, Clinical Genetics, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

McKenzie Wells (M)

Department of Neurology, University of Pennsylvania, Philadelphia, PA 19104, USA.

Natalia Wisniewski (N)

Obstetrics and Gynecology Reproductive Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Renee Wright (R)

Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Elisabeth McCarty Wood (EM)

Penn Telegenetics Program, University of Pennsylvania, Philadelphia, PA 19104, USA.

Stacy Woyciechowski (S)

Division of Cardiology, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Kristin Zelley (K)

Division of Oncology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

Kathleen D Valverde (KD)

Master of Science in Genetic Counseling Program, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.

Donna M McDonald-McGinn (DM)

22q and You Center, Clinical Genetics, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Human Biology and Medical Genetics, Sapienza University, 00185 Rome, Italy.

Classifications MeSH