Laura Hendon

Laura Hendon

Associate Professor

Department:
SOM-Peds-Genetics

Email:
lhendon@umc.edu

Work Phone:
(601) 815-4487

Biography

Laura Godfrey Hendon is an Associate Professor of Pediatrics and Ob-Gyn at UMMC where she is a certified genetic counselor with 14 years of experience providing genetic counseling across the lifespan. She was the first prenatal genetic counselor in Mississippi. She is actively engaged in medical education, clinical research, and student supervision. Laura holds leadership positions within the National Society of Genetic Counselors and is a member of the Association of Professors of Human and Medical Genetics. She is particularly passionate about revising genetics education at UMMC where she serves as the Faculty supervisor of the Genetics Special Interest Group. Laura serves on multiple committees at UMMC including Faculty Focus, Faculty Senate, GWIMS, and the Curriculum Development and Innovation Subcommittee. She is a member of the Academy for Excellence in Education and a past winner of AGCPD’s Outstanding Clinical Supervisor Award. Laura received her MA in Molecular Genetics and Genomics from Washington University in St. Louis and her MS in Genetic Counseling from the University of Texas Health Science Center in Houston.

Education

University of Texas Health Science Center at Houston, MS, Genetic Counseling2011
Washington University in Saint Louis, MA, Biomedical Sciences2008
University of Mississippi, BS, Biology2006

Specialty Certification Licensure

Licensure, Genetic Counseling State License02/2026 - 02/2028
Certification, Certified Genetic Counselor, American Board of Genetic Counseling12/2022 - 12/2027

Current Positions

Associate Professor, School of Medicine, Department of Pediatrics07/2022 - Present
Associate Professor, School of Medicine, Department of Obstetrics and Gynecology07/2022 - Present
The University of Mississippi Medical Center
Jackson, Mississippi 39216

Academic Appointments or Other Previous Appointments

Assistant Professor, University of Mississippi Medical Center, School of Medicine, Department of Pediatrics10/2017 - 06/2022
Assistant Professor, University of Mississippi Medical Center, School of Medicine, Department of Obstetrics and Gynecology10/2017 - 06/2022

Sponsored Program Funding

Extramural, Expanding Prenatal cell-free DNA screening Across monogenic Disorders (EXPAND) Study, Natera06/2025 - Present
Extramural, Project Baby Magnolia (PBM) Research Team and Project Baby Magnolia Scholars (PBMS) Clinical Liaison and Student Supervisor, UMMC Molecular Center for Health and Disease (MCHD) Core A07/2024 - Present
Extramural, Return of Genomic Results and Aggregate Penetrance in Population-Based Cohorts, Brigham & Women's Hospital, NIH/NHLBI02/2021 - 08/2023
Extramural, Clinical sequencing across communities in the Deep South, NIH/NHGRI10/2017 - 05/2021
Extramural, Perinatal Exposures and Maternal Factors Responsible for Critical Congenital Heart Defects in Mississippi, National Instititue of General Medical Sciences06/2017 - 05/2020

Publications

Journal Article

Asadollahi R, Ahmad A, Boonsawat P, Shahanoor Hinzen J, Lohse M, Bouazza-Arostegui B, Sun S,
Utesch T, Sommer JD, Ilic D, Padmanarayana M, Fischermanns K, Ranjan M, Boll M, Ka C, Piton A,
Mattioli F, Isidor B, Õunap K, Reinson K, Wojcik MH, Marshall CR, Mercimek-Andrews S,
Matsumoto N, Miyake N, Stephan BO, Honjo RS, Bertola DR, Kim CA, Yusupov R, Mefford HC,
Christodoulou J, Lee J, Heath O, Brown NJ, Baker N, Stark Z, Delatycki M, Lake NJ, Zeidler S,
Zuurbier L, Maas SM, de Kruiff CC, Rajabi F, Rodan LH, Coury SA, Platzer K, Oppermann H, Abou
Jamra R, Beblo S, Maxton C, Śmigiel R, Underhill H, Dubbs H, Rosen A, Helbig KL, Helbig I,
Ruggiero SM, Fitzgerald MP, Kraemer D, Prada CE, Tenney J, Jayakar P, Redon S, Lefranc J, Uguen K,
Race S, Efthymiou S, Maroofian R, Houlden H, Coppens S, Deconinck N, Ashokkumar B, Varalakshmi
P, Gowda K VR, Eghbal F, Ghayoor Karimiani E, Heidari M, Neidhardt J, Owczarek-Lipska M,
Korenke GC, Bamshad MJ, Campeau PM, Lehman A, Hendon LG, Wentzensen IM, Mona Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function. Nature Genetics. November 2025.
2025
Spangenberg M, Hendon LG, Goodloe DH, Brewer F, Zhai G, Gomes A. Prenatal genetic counseling challenges with indeterminate SMA results. Journal of Genetic Counseling. April 2025.2025
McBride A, Cannon A, Prakash S, Roberts AW, Seasely A, Hurst ACE, Hendon L. Cell-free DNA results indicating mosaic monosomy X of likely maternal origin: impact on genetic counseling practices and patient experiences. Prenatal Diagnosis. April 2025.2025
Favier M, Brischoux-Boucher E, Pyle LC, Mottet N, Auber-Lenoir M, Cattin J, Dahlen E, Cabrol C,
Arbez-Gindre F, Attié-Bitach T, Boute O, Devisme L, Trost D, Boughalem A, Chitayat D, Prasov L,
Chorin O, Rein-Rothschild A, Kassif E, Weissbach T, Hendon LG, Adam MP, Quelin C, Jaillard S,
Mary L, Aukema SM, Heijligers M, de Die-Smulders C, Stegmann S, Badalato L, Ben-Yehuda A,
Beneteau C, Forey PL, Kuentz P, Piard J. Fetal presentation of MYRF-related cardiac urogenital syndrome: an emerging and challenging prenatal diagnosis. Prenatal Diagnosis. December 2024.
2024
Alia Tayara, Laura G Hendon, Shelby Barrera, Jeffrey Carron. Middle ear fibrosis contributes to hearing loss in patients with Myhre syndrome. Ear, Nose, and Throat Journal. June 2024.2024
Stephanie A Felker, James M J Lawlor, Susan M Hiatt, Michelle L Thompson, Donald R Latner,
Candice R Finnila, Kevin M Bowling, Zachary T Bonnstetter, Katherine E Bonini, Nicole R Kelly,
Whitley V Kelly, Anna C E Hurst, Salman Rashid, Melissa A Kelly, Ghunwa Nakouzi, Laura G
Hendon, E Martina Bebin, Eimear E Kenny, Gregory M Cooper. Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testing. Genetics in Medicine. August 2023.
2023
Lemke AA, Thompson ML, Gimpel EC, McNamara KC, Rich CA, Finnila CR, Cochran ME, Lawlor
JMJ, East KM, Bowling KM, Latner DR, Hiatt SM, Amaral MD, Kelley WV, Greve V, Gray DE, Felker
SA, Meddaugh H, Cannon A, Luedecke A, Jackson KE, Hendon LG, Janani HM, Johnston M, Merin
LA, Deans SL, Tuura C, Hughes T, Williams H, Laborde K, Neu MB, Patrick-Esteve J, Hurst ACE,
Kirmse BM, Savich R, Spedale SB, Knight SJ, Barsh GS, Korf BR, Cooper GM, Brothers KB. Parents' perspectives on the utility of genomic sequencing in the neonatal intensive care unit. Personalized Medicine. June 2023.
2023
Kevin M. Bowling, Michelle L. Thompson, Melissa A. Kelly, Sarah Scollon, Anne M. Salvotinek,
Bradford C. Powell, Brian M. Kirmse, Laura G. Hendon, Kyle B. Brothers, Bruce R. Korf, Gregory M.
Cooper, John M. Greally and Anna C.E. Hurst. Return of non-ACMG recommended incidental genetic findings to pediatric patients: considerations and opportunities from experience in genomic sequencing. Genome Medicine. November 2022.
2022
Gerarda Cappuccio, Simona Brillante, Roberta Tammaro, Michele Pinelli, Margherita Lucia De
Bernardi, Maria Grazia Gensini, Emilia K Bijlsma, Tamara T Koopmann, Mariette J V Hoffer,
Kimberly McDonald, Laura G Hendon, Sofia Douzgou, Charulata Deshpande, Stefano D’Arrigo,
Annalaura Torella, Vincenzo Nigro, Brunella Franco, Nicola Brunetti-Pierri. Biallelic variants in CENPF causing a phenotype distinct from Stromme syndrome. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. April 2022.
2022
Kyle B. Brothers, Carla A. Rich, Emily C. Gimpel, Kelly M. East, Meagan E. Cochran, Veronica Greve, Whitley V. Kelley, Kelly E. Jackson, Laura G. Hendon, Amanda Luedecke, Hillary M. Janani, Hannah Meddaugh, Donald R. Latner, Kevin M. Bowling, Michelle L. Thompson, Candice R. Finnila, Susan M. Hiatt, Michelle D. Amaral, James M.J. Lawlor, David E. Gray, Stephanie A. Felker, Ashley Cannon, Marla Johnston, Lee Ann Merin, Sarah L. Deans, Carly Tuura, Heather Williams, Kelly Laborde, Matthew B. Neu, Jessica Patrick-Esteve, Anna C.E. Hurst, Jegen Kandasamy, Waldemar A. Carlo, Brian M. Kirmse, Renate Savich, Duane Superneau, Steven B. Spedale, Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper Genome sequencing as a first-line diagnostic test for hospitalized infants. Genetics in Medicine. 2021 September 11.2021
Boothe E, West B, Hendon L, Kaplan J, and B Kirmse. Asynchronous Telemedicine for Clinical Genetics Consultations in the NICU: A Single Center's Solution J Perinatol. 2021 July 23. Online ahead of print.2021
Suckiel, S.A.; O'Daniel, J.M.; Donohue, K.E.; Gallagher, K.M.; Gilmore, M.J.; Hendon, L.G.; Joseph, G.; Lianoglou, B.R.; Mathews, J.M.; Norton, M.E. Genomic Sequencing Results Disclosure in Diverse and Medically Underserved Populations: Themes, Challenges, and Strategies from the CSER Consortium Journal of Personalized Medicine. 11(3)2021
Van Dijck A, Vulto-van Silfhout AT, Cappuyns E, van der Werf IM, Mancini GM, Tzschach A, Bernier R, Gozes I, Eichler EE, Romano C, Lindstrand A, Nordgren A; ADNP Consortium, Kvarnung M, Kleefstra T, de Vries BBA, Küry S, Rosenfeld JA, Meuwissen ME, Vandeweyer G, Kooy RF.
Collaborators: Bakshi M, Wilson M, Berman Y, Dickson R, Fransen E, Helsmoortel C, Van den Ende J, Van der Aa N, van de Wijdeven MJ, Rosenblum J, Monteiro F, Kok F, Quercia N, Bowdin S, Dyment D, Chitayat D, Alkhunaizi E, Boonen SE, Keren B, Jacquette A, Faivre L, Bezieau S, Isidor B, Rieß A, Moog U, Lynch SA, McVeigh T, Elpeleg O, Smeland MF, Fannemel M, van Haeringen A, Maas SM, Veenstra-Knol HE, Schouten M, Willemsen MH, Marcelis CL, Ockeloen C, van der Burgt I, Feenstra I, van der Smagt J, Jezela-Stanek A, Krajewska-Walasek M, González-Lamuño D, Anderlid BM, Malmgren H, Nordenskjöld M, Clement E, Hurst J, Metcalfe K, Mansour S, Lachlan K, Clayton-Smith J, Hendon LG, Abdulrahman OA, Morrow E, McMillan C, Gerdts J, Peeden J, Schrier Vergano SA, Valentino C, Chung WK, Ozmore JR, Bedrosian-Sermone S, Dennis A, Treat K, Hughes SS, Safina N, Le Pichon JB, McGuire M, Infante E, Madan-Khetarpal S, Desai S, Benke P, Krokosky A, Cristian I, Baker L, Gripp K, Stessman HA, Eichenberger J, Jayakar P, Pizzino A, Manning MA, Slattery L. Clinical presentation of a complex neurodevelopmental disorder caused by mutations in ADNP Biological Psychiatry. 85(4):287-297
2018
Pena LDM, Jiang YH, Schoch K, Spillmann RC, Walley N, Stong N, Rapisardo Horn S, Sullivan JA, McConkie-Rosell A, Kansagra S, Smith EC, El-Dairi M, Bellet J, Keels MA, Jasien J, Kranz PG, Noel R, Nagaraj SK, Lark RK, Wechsler DSG, Del Gaudio D, Leung ML, Hendon LG, Parker CC, Jones KL, Undiagnosed Diseases Network Members, Goldstein DB, Shashi V Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases Genetics in Medicine. 20(4):464-469.2017
Morris CA, Mervis CB, Paciorkowski AP, Abdul-Rahman O, Dugan SL, Rope AF, Bader P, Hendon LG, Velleman SL, Klein-Tasman BP, Osborne LR 7q11.23 duplication syndrome: physical characteristics and natural history American Journal of Medical Genetics Part A. 167A(12):2916-35.2015
Vandeweyer G, Helsmoortel C, Van Dijck A, Vulto-van Silfhout AT, Coe BP, Bernier R, Gerdts J, Rooms L, van den Ende J, Bakshi M, Wilson M, NOrdgren A, Hendon LG, Abdulrahman OA, Romano C, de Vries BB, Kleefstra T, Eichler EE, van der Aa N, Kooy RF The transcriptional regulator ADNP links the BAF (SWI/SNF) complexes with autism American Journal of Medical Genetics C Seminars in Medical Genetics. 166C(3):315-262014
Reisch N, Idkowiak J, Hughes BA, Ivison HE, Abdul-Rahman OA, Hendon LG, Olney AH, Nielsen S, Harrison R, Blair EM, Dhir V, Krone N, Shackleton CH, Arlt W Prenatal diagnosis of congenital adrenal hyperplasia caused by P450 oxidoreductase deficiency Journal of Clinical Endocrinology and Metabolism, 2013, 98(3).2013
Cahan P, Godfrey LE, Eis PS, Richmond TA, Selzer, RR, Brent M, McLeod HL, Ley TJ, Graubert TA wuHMM: a robust algorithm to detect DNA copy number variation using long oligonucleotide microarray data Nucleic Acids Research. 2008. 36(7)2008

Abstracts

Rajeevi Madankumar; Thomas Westover; Luis D. Pacheco; Mollie McDonnold; Jessica Scholl; Lawrence D. Platt; Ravindu P. Gunatilake; Olaide Ashimi Balogun; Angela T. Bianco; Laura G. Hendon; Todd Rosen; Ashley S. Roman; Karen Fitch; Karin Niemeyer; Ravi Vijaya Satya; Ebad Ahmed; Xingwu Lu; Wenbo Xu; Hyunseok P. Kang; Fergal Casey; Matthew Rabinowitz; Emily Morton; Vivienne Souter; Jeffrey T. Meltzer; John Williams, III. Performance of a Single Gene Non-Invasive Prenatal Screening Test for Recessive Conditions. Society of Maternal Fetal Medicine 2026 Pregnancy Meeting Oral Abstracts.2026
Donald R. Latner, Kevin M. Bowling, Michelle L. Thompson, Candice R. Finnila, Susan M. Hiatt, Michelle D. Amaral, James M.J. Lawlor,Kelly M. East, Meagan E. Cochran, Veronica Greve, Whitley V. Kelley, 1David E. Gray, Stephanie A. Felker, Hannah Meddaugh, Ashley Cannon, Amanda Luedecke, Kelly E. Jackson, Laura G. Hendon, Hillary M. Janani, Marla Johnston, Lee Ann Merin, Sarah L. Deans, Carly Tuura, Heather Williams, Kelly Laborde, Matthew B. Neu, Jessica Patrick-Esteve, Anna C.E. Hurst, Jegen Kandasamy, Wally Carlo, Kyle B. Brothers, Brian M. Kirmse, Renate Savich, Duane Superneau, Steven B. Spedale, 8Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper SouthSeq: Genome Sequencing for a Diverse Population of Hospitalized Infants American College of Medical Genetics (ACMG) Annual Meeting 20222022
Michelle L. Thompson, Kevin M. Bowling, Donald R. Latner, Candice R. Finnila, Susan M. Hiatt, Michelle D. Amaral, Whitley V. Kelley, Kelly M. East, Veronica Greve, Meagan E. Cochran, David E. Gray, James M.J. Lawlor, Hannah Meddaugh, Ashley Cannon, Amanda Luedecke, Kelly E. Jackson, Laura G. Hendon, Hillary M. Janani, Marla Johnston, Lee Ann Merin, Sarah L. Deans, Carly Tuura, Trent Hughes, Heather Williams, Kelly Laborde, Matthew Neu, Jessica Patrick-Esteve, Anna C.E. Hurst, Kyle B. Brothers, Renate Savich, Steven B. Spedale, 7Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper Genome sequencing as a frontline test in ill newborns American Society of Human Genetics (ASHG) Annual Meeting 20212021
Michelle D. Amaral, Michelle L. Thompson, Kevin M. Bowling, Candice R. Finnila, Susan M. Hiatt, Donald R. Latner, Whitley V. Kelley, Kelly M. East, Veronica Greve, Meagan E. Cochran, David E. Gray, James M.J. Lawlor, Hannah Meddaugh, Ashley Cannon, Amanda Luedecke, Kelly E. Jackson, Laura G. Hendon, Hillary M. Janani, Marla Johnston, Lee Ann Merin, Sarah L. Deans, Carly Tuura, Kelly Laborde, Jessica Patrick-Esteve, Anna C.E. Hurst, Kyle B. Brothers, Trent Hughes, Heather Williams, Renate Savich, Steven B. Spedale, Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper SouthSeq: Genome sequencing as a first-tier genetic test in the NICU American College of Medical Genetics (ACMG) Annual Meeting 2021 (virtual)2021
Sabrina A. Suckiel, Julianne M. O'Daniel, Katherine E. Donohue, Katie M. Gallagher, Marian J. Gilmore, Laura G. Hendon, Galen Joseph, Billie Lainoglou, Jennifer Matthews, Mary E. Norton, Jacqueline A. Odgis, Alexis F Poss, Shannon Rego, Sarah Scollon, Tiffany Yip, and Laura M. Amendola. Genomic sequencing results disclosure in diverse and medically underserved populations: themes, challenges, and strategies from the CSER consortium. American College of Medical Genetics (ACMG) Annual Meeting 20212021
Gerarda Cappuccio, Maria Grazia Gensini1, Sofia Douzgou, Emilia K Bijlsma, Laura Hendon, Bertrand Isidor, Cogne Benjamin, Michele Pinelli, Annalaura Torella, Vincenzo Nigro, Nicola Brunetti-Pierri Core clinical features of CENPF-related disorder European Human Genetics Conference (ESHG) 2020 (virtual)2020
Kevin M. Bowling, Susan M. Hiatt, Candice R. Finnila, Michelle L. Thompson, Donald R. Latner, Michelle D. Amaral, Kelly M. East, Meagan E. Cochran, Veronica N. Greve, Whitley V. Kelley, David E. Gray, James M. Lawlor, Laura G. Hendon, Hillary Wienpahl, Kyle B. Brothers, Anna C. Hurst, Renate Savich, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper SouthSeq: Sequencing NICU Newborns in the South American College of Medical Genetics (ACMG) Annual Meeting 2020 (virtual)2020
Meagan Cochran, Kelly East, Veronica Greve, Whitley Kelley, Candice Finnila, Laura Hendon, Hillary Janani, Elizabeth Rahn, Joshua Melnick, Maria I. Danila, Renate Savich, Kyle Brothers, Steven Spedale, Jessica Patrick-Esteve, Brian Sims, Waldemar Carlo, Greg Barsh, Bruce Korf, Greg Cooper Putting It Into Practice: Tracking Errors In Disclosures Of Genome Sequencing Results In The NICU By Trained Non-Genetics Providers American College of Medical Genetics (ACMG) Annual Meeting 2020 (virtual)2020
Michelle D. Amaral, Michelle L. Thompson, Kevin M. Bowling, Candice R. Finnila, Susan M. Hiatt, Donald R. Latner, Whitley V. Kelley, Kelly M. East, Veronica Greve, Meagan E. Cochran, David E. Gray, James M.J. Lawlor, Hannah Meddaugh, Ashley Cannon, Amanda Luedecke, Kelly E. Jackson, Laura G. Hendon, Hillary M. Janani, Marla Johnston, Lee Ann Merin, Sarah L. Deans, Carly Tuura, Kelly Laborde, Jessica Patrick-Esteve, Anna C.E. Hurst, Kyle B. Brothers, Trent Hughes, Heather Williams, Renate Savich, Steven B. Spedale, Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper SouthSeq: Genome sequencing as a first-tier genetic test in the NICU American College of Medical Genetics (ACMG) Annual Meeting 2020 (virtual)2020
Kelly East, Meagan Cochran, Veronica Greve, Whitley Kelley, Ashley Cannon, Laura Hendon, Hillary Weinpahl, Candice Finnila, Kevin Bowling, Anna Hurst, Sara Knight, Elizabeth Rahn, Maio Danila, Renate Savich, Greg Barsh, Bruce Korf, Greg Cooper Non-genetics Healthcare Provider Training to Deliver Whole-Genome Sequencing Results National Society of Genetic Counselors (NSGC) Annual Conference 20192019
Anna Hurst, Ashley Cannon, Kelly East, Meagan Cochran, Veronica Greve, Whitley Kelley, Candice Finnila, Kevin Bowling, Michelle Thompson, Adam Hott, Laura Hendon, Brian Kirmse, Renate Savich, Hillary Weinpahl, Sara Knight, Elizabeth Rahn, Maria I. Danila, Greg Barsh, Bruce Korf, Greg Cooper SouthSeq: Genome Sequencing for Infants in NICUs Across the Deep South Southeastern Regional Genetics Group (SERGG) Annual Meeting 20192019
Kevin M. Bowling, Susan M. Hiatt, Candice R. Finnila, Michelle L. Thompson, Michelle D. Amaral, Whitley V. Kelley, Kelly M. East, David E. Gray, James M. Lawlor, Laura G. Hendon, Hillary Wienpahl, Kyle B. Brothers, Anna C. Hurst, Renate Savich, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper Preliminary Results of SouthSeq: Sequencing NICU Newborns in the South American College of Medical Genetics (ACMG) Annual Meeting 20192019
Kyle B. Brothers, Carla A. Rich, Emily C. Gimpel, Kelly M. East, Meagan E. Cochran, Veronica Greve, Whitley V. Kelley, Kelly E. Jackson, Laura G. Hendon, Amanda Luedecke, Hillary M. Janani, Hannah Meddaugh, Donald R. Latner, Kevin M. Bowling, Michelle L. Thompson, Candice R. Finnila, Susan M. Hiatt, Michelle D. Amaral, James M.J. Lawlor, David E. Gray, Stephanie A. Felker, Ashley Cannon, Marla Johnston, Lee Ann Merin, Sarah L. Deans, Carly Tuura, Heather Williams, Kelly Laborde, Matthew B. Neu, Jessica Patrick-Esteve, Anna C.E. Hurst, Jegen Kandasamy, Waldemar A. Carlo, Brian M. Kirmse, Renate Savich, Duane Superneau, Steven B. Spedale, Sara J. Knight, Gregory S. Barsh, Bruce R. Korf, Gregory M. Cooper Parental Impact of Genome Sequencing During the Neonatal Period American College of Medical Genetics (ACMG) Annual Meeting 2022

Presentations

National and International Invited Seminars/Lectures, Patient-Provider Panel: Real Stories, Real Impact., Natera, Anaheim, California01/2026
State/Local Invited Seminars/Lectures, The evolving landscape of non-invasive prenatal screening: cell free DNA in 2025., Department of Pediatrics, UMMC Jackson12/2025
Presentation to UMMC GWIMS Chapter, Pumpkin pie and pedigrees: the importance of knowing your family health history., UMMC Chapter of the Group on Women in Medicine and Science (GWIMS), UMMC- Jackson11/2025
National and International Invited Seminars/Lectures, The evolving landscape of inherited conditions: from carrier status to clinical manifestations and NIPT., National Society of Genetic Counselors, Seattle, Washington11/2025
State/Local Invited Seminars/Lectures, The evolving landscape of non-invasive prenatal screening: cell free DNA in 2025., Newborn Associates, River Hills Country Club, Jackson, MS07/2025
Presentation to UMMC's Summer Genetics and Omics Academy, Advances in perinatal/pediatric genetic testing., Molecular Center for Health and Disease (MCHD), UMMC-Jackson07/2025
State/Local Invited Seminars/Lectures, A decade of discovery: (most) everything you need to know about non-invasive prenatal screening in 2025., UMMC Department of OB-Gyn, UMMC- Jackson05/2025
National and International Invited Seminars/Lectures, Navigating unexpected cell free DNA findings in the pregnant patient: laboratory and clinical perspectives. Part 2., National Society of Genetic Counselors, Virtual (Webinar)04/2025
State/Local Invited Seminars/Lectures, A call for collaboration: ascertainment of maternal malignancy via cell free DNA aneuploidy screening., UMMC Department of Ob-Gyn, UMMC- Jackson04/2025
National and International Invited Seminars/Lectures, Navigating unexpected cell free DNA findings in the pregnant patient: laboratory and clinical perspectives. Part 1., National Society of Genetic Counselors (NSGC), Virtual (Webinar)08/2024
Presentation to UMMC's Summer Genetics and Omics Academy, Advances in perinatal/pediatric genetic testing., UMMC Molecular Center for Health and Disease (MCHD), UMMC- Jackson07/2024
State/Local Invited Seminars/Lectures, Unusual variances, low fetal fraction, and atypical findings- oh my! Navigating abnormal NIPT results in the first trimester., Department of Ob-Gyn, River Hills Country Club03/2024
State/Local Invited Seminars/Lectures, Non invasive prenatal screening and genetic counseling., Mississippi Academy of Sciences, University of Southern Mississippi03/2024
Presentation to UMMC School of Nursing Journal Club, Clinical genetics research at UMMC: SouthSeq, PopSeq, and Baby Magnolia., UMMC School of Nursing, UMMC- Jackson08/2023
National and International Invited Seminars/Lectures, Expanded NIPT: genetic counseling concerns., International Society of Prenatal Diagnosis, Virtual (Webinar)06/2022
Poster Presentation, Whole genome sequencing and the identification of dual genetic diagnoses in complex phenotypes in the NICU, National Society of Genetic Counselors Annual Conference, New Orleans, Louisiana09/2021
Regional Invited Seminars/Lectures, Navigating the genetic testing ordering process, Project ECHO, Virtual- Project ECHO07/2021
Regional Invited Seminars/Lectures, Chromosomes: laying the foundation for understanding aneuploidy and basic genetic testing., Project ECHO, Virtual- Project ECHO04/2021
National and International Invited Seminars/Lectures, Student supervision: let's talk about anxiety and perfectionism., National Society of Genetic Counselors Annual Conference, Virtual11/2020
Poster Presentation, Genome sequencing and the challenges of the rare diagnosis in the NICU setting, National Society of Genetic Counselors Annual Conference, Virtual11/2020
National and International Invited Seminars/Lectures, So much more than a gender test: navigating the brave new world of non-invasive prenatal screening., Medical Education Without Borders, Virtual10/2020
State/Local Invited Seminars/Lectures, Genetic counseling: career overview and case examples, Germantown High School01/2020
Poster Presentation, Recurrent Non-Immune Fetal Hydrops (NIFH) due to Native American Myopathy (NAM) in an African-American Couple: Expanding the Phenotype of STAC3-related Congenital Myopathy, National Society of Genetic Counselors Annual Conference, Salt Lake City, Utah11/2019
Poster Presentation, Integrating Genomics Research with Clinical Care in the NICU Setting, National Society of Genetic Counselors Annual Conference, Salt Lake City, Utah11/2019
Invited Symposia, Genetics and CHDs, UMMC, UMMC Classroom Wing06/2019
Invited Symposia, Congenital heart disease, Mississippi State Department of Health, UMMC Conference Center05/2019
State/Local Invited Seminars/Lectures, Genetic Counseling, Madison Central High School01/2019
State/Local Invited Seminars/Lectures, Genetic counseling and patterns of inheritance, Bailey APAC Middle School, Jackson, Mississippi02/2018
State/Local Invited Seminars/Lectures, Pedigree analysis, Madison County School Teachers Education, Jackson, Mississippi07/2016
Invited Symposia, First trimester screening: from NT to NIPT., Annual UMMC-Wiser Society Ultrasound Symposium, Ridgeland, Mississippi04/2016
National and International Invited Seminars/Lectures, Non-invasive prenatal screening, American College of Osteopathic Obstetricians and Gynecologists 2014 Fall Educational Conference, Fort Worth, Texas10/2014
Regional Invited Seminars/Lectures, Henry Pace Commemorative Luncheon Lecture. Medical Genetics: Hereditary Breast and Ovarian Cancer Syndromes, Mississippi Osteopathic Medical Association 2014 Annual Coast Conference, Destin, Florida05/2014
State/Local Invited Seminars/Lectures, Specific Indications of Medical Genetics in Clinical Practice, Missippi Osteopathic Medical Association (MOMA) Winter CME Meeting, Biloxi, Mississippi02/2014
Poster Presentation, Genetic counselors in the community: Establishing a perinatal support group, National Society of Genetic Counselors Annual Education Conference, Anaheim, California10/2013
State/Local Invited Seminars/Lectures, Genetic counseling: information for your practice, Mississippi Department of Health, Jackson, Mississippi11/2011
Poster Presentation, Physician perceptions of risk regarding mood disorders and pharmacological management during pregnancy: What is current practice?, National Society of Genetic Counselors Annual Education Conference, San Diego, California10/2011

Honors, Awards, and Recognition

Induction into the Academy for Excellence in Education, Academy for Excellence in Education2023
Trailblazer Teaching Award 2019-2020, University of Mississippi Medical Center- Office of Medical Education2020
Outstanding Clinical Supervisor Award- University of Alabama at Birmingham, Association of Genetic Counseling Program Directors (AGCPD)2019

Professional Membership and Service

Association of Professors of Human and Medical Genetics (APHMG), Member2024 - 2025
NSGC Prenatal Special Interest Group, Member, Continuing Service, National Organization2012 - Present
American Board of Genetic Counseling, Member2011 - Present
National Society of Genetic Counselors, Member, Continuing Service, National Organization2009 - Present

Committee Service

SCHOOL OF MEDICINE-GROUP ON WOMEN IN MEDICINE AND SCIENCE, President2025 - Present
Academy for Excellence in Education, Task Force Member2024 - Present
MEDICAL CENTER-FACULTY SENATE, Task Force Chair2024 - Present
SCHOOL OF MEDICINE-GROUP ON WOMEN IN MEDICINE AND SCIENCE, Co-Chair2024 - 2025
MEDICAL CENTER-FACULTY SENATE, Member2024 - Present
MEDICAL CENTER-FACULTY FOCUS COMMITTEE, Chair2024 - Present
SCHOOL OF MEDICINE-CURRICULUM - DEVELOPMENT AND INNOVATION SUBCOMMITTEE, Member2023 - Present
SCHOOL OF MEDICINE-ADMISSIONS FILE REVIEW SUBCOMMITTEE, Member2021 - Present

Community Service

UMMC Rare Disease Day Research Symposium, Founder/Organizer02/2025 - 02/2025
Madison County High School Academy of Engineering and Biomedical Sciences Advisory Board, Advisory Board Member01/2025 - Present
UMMC Pediatric Research Day, Volunteer Poster Judge07/2024 - 07/2024
Central Mississippi Down Syndrome Society Buddy Center, Volunteer03/2024 - 03/2024
Rare Disease Awareness Day at UMMC, Founder/Organizer02/2024 - 02/2024
Central Mississippi Down Syndrome Society Buddy Center, Volunteer03/2023 - 03/2023
Rare Disease Awareness Day at UMMC, Founder/Organizer02/2023 - 02/2023
Question It? Discover It! Mississippi Children's Museum, Volunteer Instructor11/2022 - 11/2022
Girl Scouts of Greater Mississippi, Daisy and Brownie Troop Leader (4378, 4379)09/2021 - 05/2023
Question It? Discover It! Mississippi Children's Museum, Volunteer Instructor10/2020 - 10/2020
Genetics Day at MS Children's Museum, Volunteer09/2019 - 09/2019
Run Up for Downs Race, Team Captain03/2019 - 03/2019
Genetics Day at MS Children's Museum, Volunteer09/2018 - 09/2018
22q at the Zoo, Volunteer05/2018 - 05/2018
TSC Step Forward Walk, Participant05/2018 - 05/2018
Run Up for Downs Race, Team Captain03/2018 - 03/2018
DNA Day at MS Children's Museum, Volunteer06/2017 - 06/2017
22q at the Zoo, Volunteer05/2017 - 05/2017
Central MS Buddy Walk, Participant10/2016 - 10/2016
22q at the Zoo, Volunteer05/2016 - 05/2016
Run Up for Downs Race, Participant03/2016 - 03/2016
Run Up for Downs Race, Participant03/2015 - 03/2015
Run Up for Downs Race, Participant03/2014 - 03/2014
Run Up for Downs Race, Participant05/2013 - 05/2013
High Hopes Farm Therapeutic Horseback Riding Program, Volunteer Coordinator/Head Volunteer10/2012 - 10/2017

Other Service

State of Mississippi Genetic Counseling Licensure Board, Board Member2026 - Present
NSGC Education Committee, Chair2026 - Present
NSGC Education Committee, Vice Chair2025 - 12/2025
NSGC Abstract Working Group, Chair2024 - 12/2024
University of Alabama at Birmingham (UAB) Genetic Counseling Program External Course Reviewer- GC504: Embryology, Teratology, and Prenatal Genetics, External Course Reviewer12/2023 - Present
University of Alabama at Birmingham (UAB) Genetic Counseling Training Program (GCTP) Research Projects Committee, Member08/2023 - Present
NSGC Abstract Working Group, Vice Chair2023 - 12/2023
UMMC School of Medicine (SOM) Genetics Special Interest Group (SIG), Faculty Advisor08/2022 - Present
NSGC Prenatal SIG Literature Review Committee, Curate and disseminate journal articles to special interest group2020 - Present
NSGC NSGCares Committee Member, Organize and excecute volunteer activies that support inclusiveness in our community and promote genetic counselors12/2019 - 12/2021
NSGC Abstract Working Group Member, Review abstracts02/2019 - 12/2022
NSGC NSGConnect Mentor, Mentor to junior genetic counselor10/2018 - Present
NSGC Prenatal SIG Education Committee Chair, Comittee Chair, recruit, advise, and coorindate speakers for annual conference and online webinar series12/2012 - 12/2015

Teaching Experience

Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2026 - 2026
Medicine, M3 Small Groups FacilitatorSpring 2026 - 2026
Lecture, Lecturer, SOM 622Fall 2025
Medicine, Lecture, Lecturer, OB-Gyn Residents LectureSpring 2025 - 2025
Medicine, Small Group, Facilitator, M1 History Taking Small Group WorkshopsFall 2024 - 2024
Medicine, Lecture, Lecturer, M2Fall 2024 - 2024
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2024 - 2024
Medicine, Lecture, Lecturer, M3 Ob-Gyn Clerkship Lecture: Genetics and genetic disorders in Ob-GynSpring 2023-present
Medicine, Lecture, Lecturer, SOM 610Fall 2023, 2024, 2025
Medicine, Lecture, Lecturer, Pediatric Residents LectureSummer 2023 - 2023
Medicine, Lecture, Lecturer, Maternal Fetal Medicine Fellows DidacticsSpring 2023 - 2023
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2023 - 2023
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2022 - 2022
Medicine, Lecture, Lecturer, M1 StudentsFall 2021 and 2022
Medicine, Lecture, Lecturer, M1 LectureFall 2021 and 2022
Medicine, Small Group, Facilitator, M1 Small Group WorkshopsFall 2021 and 2022
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2021 - 2021
Medicine, Lecture, Lecturer, M3 Ob-Gyn Clerkship Lecture: Genetics and genetic disorders in Ob-GynSpring 2021 - 2021
Graduate, Lecture, Lecturer, Intrauterine fetal desmise (IUFD).Spring 2021 - 2021
Medicine, Lecture, Lecturer, M3 Ob-Gyn Clerkship Lecture: Genetics and genetic disorders in Ob-GynSpring 2021 - 2021
Medicine, Lecture, Lecturer, M3 Ob-Gyn Clerkship Lecture: Genetics and genetic disorders in Ob-GynSpring 2021 - 2021
Medicine, Lecture, Lecturer, M3 Ob-Gyn Clerkship Lecture: Genetics and genetic disorders in Ob-GynFall 2021 - 2021
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2021 - 2021
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2021 - 2021
Medicine, Lecture, Lecturer, M3 Ob-Gyn Clerkship Lecture: Genetics and genetic disorders in Ob-GynFall 2021 - 2021
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2021 - 2021
Medicine, Course, Lecturer, M1 Biochemistry 610Fall 2021 - 2021
Medicine, Course, Lecturer, M1 Biochemistry 610Fall 2021 - 2021
Medicine, Course, Lecturer, M1 Biochemistry 610Fall 2021 - 2021
Medicine, Small Group, Preceptor, M1 Biochemistry 610.Fall 2021 - 2021
Medicine, Lecture, Lecturer, M3 Ob-Gyn Clerkship Lecture: Genetics and genetic disorders in Ob-GynFall 2021 - 2021
Medicine, Lecture, Lecturer, M3 Ob-Gyn Clerkship Lecture: Genetics and genetic disorders in Ob-GynFall 2021 - 2021
Graduate, Lecture, Lecturer, MFM Fellows LectureSpring 2020 - 2020
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2020 - 2020
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2020 - 2020
Medicine, Lecture, Lecturer, Pediatric Grand RoundsSpring 2020 - 2020
Medicine, Lecture, Lecturer, OB Gyn Grand RoundsFall 2020 - 2020
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2020 - 2020
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2020 - 2020
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2020 - 2020
Medicine, Lecture, Lecturer, M1 Biochemistry 610Fall 2020 - 2020
Medicine, Lecture, Lecturer, M1 Biochemistry 610Fall 2020 - 2020
Medicine, Lecture, Facilitator, M1 Biochemistry 610Fall 2020 - 2020
Medicine, Small Group, Preceptor, M1 Biochemistry 610Fall 2020 - 2020
Medicine, Lecture, Lecturer, M3 Pediatric Clerkship: Genetics ReviewFall 2020 - 2020
Medicine, Lecture, Lecturer, M3 Ob-Gyn Clerkship Lecture: Genetics and genetic disorders in Ob-GynFall 2020 - 2020
Course, Lecturer, Frate Bioethics FellowshipSummer 2019 - 2019
Graduate, Lecture, Lecturer, MFM Fellow LectureSpring 2019 - 2019
Medicine, Lecture, Lecturer, M1 Biochemistry 610Fall 2019 - 2019
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2019 - 2019
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2019 - 2019
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2019 - 2019
Course, Lecturer, Frate Bioethics FellowshipSummer 2018 - 2018
Medicine, Course, Lecturer, M2 Pathology 621Spring 2018
Medicine, Lecture, Lecturer, Nelson LectureSummer 2018 - 2018
Medicine, Lecture, Lecturer, M1 Biochemistry 610Fall 2018 - 2018
Medicine, Lecture, Lecturer, M1 Biochemistry 610Fall 2018
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2018 - 2018
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2018 - 2018
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2018 - 2018
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2018 - 2018
Graduate, Lecture, Lecturer, NICU Fellows LectureSpring 2018 - 2018
Graduate, Lecture, Lecturer, NICU Fellows LectureSpring 2018 - 2018
Graduate, Lecture, Lecturer, NICU Fellows LectureFall 2018 - 2018
Graduate, Lecture, Lecturer, NICU Fellows LectureFall 2018 - 2018
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2018 - 2018
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2018 - 2018
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2018 - 2018
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2018 - 2018
Course, Lecturer, Frate Bioethics FellowshipSummer 2017 - 2017
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2017 - 2017
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2017 - 2017
Graduate, Lecture, Lecturer, MFM Fellows LectureSpring 2017 - 2018
Graduate, Lecture, Lecturer, NICU Fellows LectureFall 2017 - 2017
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2017 - 2014
Graduate, Lecture, Lecturer, OB Gyn Residents LectureSpring 2017 - 2017
Graduate, Lecture, Lecturer, OB Gyn Residents LectureSpring 2017 - 2017
Graduate, Lecture, Lecturer, OB Gyn Residents LectureSpring 2017 - 2017
Graduate, Lecture, Lecturer, OB Gyn Residents LectureFall 2017 - 2017
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2017 - 2017
Course, Lecturer, Frate Bioethics FellowshipSummer 2016 - 2016
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2016 - 2016
Graduate, Lecture, Lecturer, MFM Fellows LectureSpring 2016 - 2017
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2016 - 2016
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2016 - 2016
Medicine, Lecture, Lecturer, OB Gyn Residents LectureSpring 2016
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2016 - 2016
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2016 - 2016
Medicine, Lecture, Lecturer, OB Gyn Residents LectureFall 2016 - 2106
Course, Lecturer, Frate Bioethics FellowshipSummer 2015 - 2015
Course, Lecturer, Frate Bioethics FellowshipSummer 2014 - 2014
Course, Lecturer, Frate Bioethics FellowshipSummer 2013 - 2013
Summer Bioethics Program, Course, Lecturer, Frate Bioethics FellowshipSummer 2012 - 2012
Graduate, Lecture, Lecturer, MFM Fellows LectureFall 2012 - 2018

Directed Student Learning

Primary (sole) supervisor, Advised: Maddie Buhl2026 - Present
Primary (sole) supervisor, Advised: Nyambi Williams2026 - Present
Master's Thesis Committee Member, Assessing management and counseling practices for patients with suspected mosaic maternal Turner syndrome detected via non-invasive prenatal testing (NIPT)
Advised: Audrey McBride
2022 - 2024
Master's Thesis Committee Member, Prenatal genetic counseling practices with indeterminate spinal muscular atrophy (SMA) results in non-Ashkenazi Jewish populations
Advised: Molly Spangenberg
2022 - 2024
Primary (sole) Supervisor, Advised: Zaria Neal2022 - 2022
Lead Supervisor, Advised: Sara Cowan2020 - 2020
Primary Supervisor, Advised: Alexis Coates2020 - 2020
Primary Supervisor, Advised: Summer Duffy2019 - 2019
Primary Supervisor, Advised: Olivia Kesler2019 - 2019
Primary Supervisor, Advised: Dora Moore2019 - 2019
Primary Supervisor, Advised: Katie Gunther2018 - 2018
Primary Supervisor, Advised: Erin McCown2017 - 2017
Supervisor, Advised: Amanda Gerard2016 - 2016
Supervisor, Advised: Angela Douglas2016 - 2016
Supervisor, Advised: Emily Boothe2013 - 2013

Fellows supervised

MFM, Lead Supervisor of Mandatory Genetics Rotation, 12 fellows supervised, MFM Genetics Elective10/2019 - Present
Maternal Fetal Medicine, QI Project Supervisor, 2 fellows supervised, QI Project01/2017 - Present