Haley M. Crane, MS, LCGC

Peer-Reviewed Publications

2025

Burrill, N., Paidas Teefey, C., Wright, R., Huynh, M., Schindewolf, E., Pilchman, L., Crane, H., Noyes, A., Roman, A., Gulersen, M., Moldenhauer, J. (January 2025). Phenotypic Expansion: Fetus with Cole-Carpenter Type 2 Presenting with Novel Neonatal Lethal Skeletal Dysplasia. American Journal of Medical Genetics Part A. 

Burrill, N., Schindewolf, E., Pilchman, L., Wright, R., Crane, H., Gebb, J., Khalek, N., Soni, S., Paidas Teefey, N., Oliver, E., Linn, R., Moldenhauer, J. (January 2025). Whole Exome Sequencing in a Population of Fetuses with Structural Anomalies. Prenatal Diagnosis.  

2024

Crane, H., Schindewolf, E., Burrill, N., Debari, S., Khalek, N., Paidas Teefey, N., Soni, S., Coleman, B., Moldenhauer, J., Gebb, J. (July 2024). Reliability of ultrasound markers in identifying fetuses with life-limiting skeletal dysplasias. Prenatal Diagnosis. PD-24-0131.R2, Epub ahead of print. 

Burrill, N., Crane, H., Khalek, N., Soni, S., Wild, K. T., Skraban, C., McManus, M., Szigety, K., Oliver, E. R., Fisher, A., Wang, J., Moldenhauer, J. S. (May 2024). Expansion of the Prenatal Phenotype of Baraitser-Winter Syndrome: Presentation of Two Cases of Multiple Congenital Anomaly Syndrome. American Journal of Medical Genetics Part A. 

Crane, H. M., Asher, S., Conway, L., Drivas, T. G., & Kallish, S. (March 2024). Unraveling a history of overlap: A phenotypic comparison of RBCK1-related disease and glycogen storage disease type IV. American Journal of Medical Genetics Part A, e63574. https://doi.org/10.1002/ajmg.a.63574  

Oral Presentations 

2024

Crane, H., Schindewolf, E., Burrill, N., DeBari, S., Khalek, N., Paidas Teefey, N., Soni, S., Coleman, B., Moldenhauer, J., Gebb, J. (February 2024). Reliability of “lethal” ultrasound markers in identifying fetuses with truly life-limited skeletal dysplasia. Society for Maternal-Fetal Medicine Annual Pregnancy Meeting, National Harbor, MD, United States.

Poster Presentations 

2025

Crane, H. M., Wright, R., Burrill, N., Pilchman, L., Gianforcaro, K., Eisenberg, G., Soni, S., Paidas Teefey, C., Wu, S., Moldenhauer, J., Gebb, J., Huynh, M., Coleman, B., Rychik, J., Khalek, N. (March 2025). Expanding the Prenatal Phenotype of MYRF-Related Cardiac-Urogenital Syndrome. American College of Medical Genetics and Genomics Annual Clinical Genetics Meeting, Los Angeles, CA, United States. 

Crane, H. M., Giardine, R., Pilchman, L., Wright, R., Gianforcaro, K., Eisenberg, G., Strong, A., Wild, K. T., Zackai, E., Dugoff, L., Sparks, T., Coleman, B., Moldenhauer, J. (March 2025). Prenatally Diagnosed Beare-Stevenson Cutis Gyrata Syndrome with a Novel Variant. American College of Medical Genetics and Genomics Annual Clinical Genetics Meeting, Los Angeles, CA, United States. 

Crane, H. M., Pilchman, L., Wright, R., Gianforcaro, K., Eisenberg, G., Paidas Teefey, C., Horii, S., Skraban, C., Strong, A., Demczko, M., Marchese, M., Szigety, K., Soni, S. (March 2025). Follow the Family History: Neonatal Diagnosis of YARSopathy and Congenital CMV. American College of Medical Genetics and Genomics Annual Clinical Genetics Meeting, Los Angeles, CA, United States. 

Crane, H. M., Pilchman, L., Wright, R., Gianforcaro, K., Eisenberg, G., Paidas Teefey, C., Huynh, M., Szwast, A., Moldenhauer, J. (March 2025). A Fetus with Diamond-Blackfan Anemia and HLHS: Expanding the Cardiac Phenotype. American College of Medical Genetics and Genomics Annual Clinical Genetics Meeting, Los Angeles, CA, United States. 

2024

Crane, H. M., Moldenhauer, J. S., Khalek, N., Gebb, J., Paidas Teefey, C., Schindewolf, E., Burrill, N., Pilchman, L., Wright, R., Borst, A. J., Fox, M. D., Coleman, B., Soni, S. (March 2024). Milroy Disease Presenting as Hydrops Fetalis: A Case Series. American College of Medical Genetics and Genomics Annual Clinical Genetics Meeting, Toronto, Canada.  

Crane, H., Schindewolf, E., Gebb, J., Burrill, N., Pilchman, L., Wright, R., DeBari, S., Coleman, B., Moldenhauer, J. (February 2024). Utility of genetic testing in fetuses with suspected lethal skeletal dysplasia on sonography. Society for Maternal-Fetal Medicine Annual Pregnancy Meeting, National Harbor, MD, United States. 

Crane, H., Schindewolf, E., Burrill, N., DeBari, S., Khalek, N., Paidas Teefey, C., Soni, S., Coleman, B., Moldenhauer, J., Gebb, J. (February 2024). Value of "lethal" ultrasound markers identifying fetuses with lethal skeletal dysplasia before/after 28 weeks. Society for Maternal-Fetal Medicine Annual Pregnancy Meeting, National Harbor, MD, United States. 

2023

DiCicco, R., Burrill, N., Crane, H., Khalek, N. Schindewolf, E., Agarwal, S, Whitehead, M., Zarrow, D., Oliver, E., Bach, A., Moldenhauer, J. (March 2023). Two cases of prenatally diagnosed Cri-du-Chat Syndrome and Associated MRI Findings. American College of Medical Genetics and Genomics Annual Clinical Genetics Meeting, Salt Lake City, UT, United States. 

2022

Crane, H., Asher, S., Conway, L., Drivas, T., Kallish, S. (October 2022). Characterizing the Natural History of RBCK1-Related Disease: A Phenotypic Comparison of Rare Disease Diagnoses. National Society of Genetic Counselors Conference, Nashville, TN, United States.

Additional Research Experience

1. Peer Reviewer: Prenatal Diagnosis 

   a. 3 manuscripts (June & September 2024, January 2025) 

Grand Rounds

2025

Crane, H., Gianforcaro, K., Budney, A., Wild, T., Khalek, N. (March 2025). Complex Antenatal Resuscitation Evaluation: Navigating Genetic Testing in the Setting of Life-Threatening Fetal Diagnoses. Children’s Hospital of Philadelphia Genetics Grand Rounds, Philadelphia, PA, United States. 

2024

Crane, H., Wright, R. (December 2024). CFDT/Pathology Rounds. Center for Fetal Diagnosis and Treatment Pathology Rounds, Philadelphia, PA, United States. 

Crane, H., Schindewolf, E., Gebb, J., Moldenhauer, J. (July 2024). Fetal skeletal dysplasia: Can we predict outcome and how does genetics aid in this pursuit? Children’s Hospital of Philadelphia Genetics Grand Rounds, Philadelphia, PA, United States. 

Strong, A., Bhoj, E., Donoghue, S., Keena, B., Crane, H., Moldenhauer, J., Zackai, E. (April 2024). Craniosynostosis and Something New for Everyone. Children’s Hospital of Philadelphia Genetics Grand Rounds, Philadelphia, PA, United States. 

Crane, H., Burrill, N. (April 2024). CFDT/Pathology Rounds. Center for Fetal Diagnosis and Treatment Pathology Rounds, Philadelphia, PA, United States. 

Wright, R., Burrill, N., Crane, H., Soni, S., Moldenhauer, J., Khalek, N. (March 2024). Genetics of Prenatally Diagnosed Micro/Anophthalmia. Children’s Hospital of Philadelphia Genetics Grand Rounds, Philadelphia, PA, United States. 

2022

Giardine, R., Presser, K., Wisniewski, N., Crane, H. (December 2022). Unexpected Results from Carrier Screening and Prenatal Diagnosis. Children’s Hospital of Philadelphia Genetics Grand Rounds, Philadelphia, PA, United States.  

Invited Lectures

2024

Crane, H., Gebb, J., Paidas Teefey, C., Wild, K. T. (June 2024). Fetal skeletal dysplasia: Can we predict outcome and what should we do if we can’t? CFDT Fetal Firesides, Children’s Hospital of Philadelphia, Philadelphia, PA, United States. 

Crane, H., Wright, R. (May 2024). Neurogenetics and Complex Malformation Syndromes. From the Start: Innovations in the Care of Fetal Anomalies Before, During, and After Birth, Children’s Hospital of Philadelphia, Philadelphia, PA, United States. 

Education/Teaching

2025

Co-Course Director for Reproductive Genetics Course (January 2025-Current), Master of Science in Genetic Counseling Program, University of Pennsylvania, Philadelphia, PA, United States.  

Crane, H. (March 2025). Fetal Intervention. Fundamentals of Genetic Counseling: Reproductive and Pediatric Care Course, Genetic Counseling Graduate Program, Kean University, Union, NJ, United States. 

2024

Crane, H. (April 2024). Assessment of Fetal Skeletal Dysplasias. Reproductive Genetics Course, Master of Science in Genetic Counseling Program, University of Pennsylvania, Philadelphia, PA, United States.