Stephanie L. Sherman

Stephanie L. Sherman

Emory & Henry College

H-index: 81

North America-United States

About Stephanie L. Sherman

Stephanie L. Sherman, With an exceptional h-index of 81 and a recent h-index of 40 (since 2020), a distinguished researcher at Emory & Henry College, specializes in the field of Down syndrome, Fragile X-associated disorders, Meiosis, Human Genetics.

His recent articles reflect a diverse array of research interests and contributions to the field:

Heritable Variation in Lymphocyte-Related Traits and Risk of Down Syndrome Acute Lymphoblastic Leukemia: A Mendelian Randomization Study

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

Genomic landscape of Down syndrome–associated acute lymphoblastic leukemia

Innovating Therapies for Down Syndrome: An International Virtual Conference of the T21 Research Society

The diagnostic experience of women with fragile X–associated primary ovarian insufficiency (FXPOI)

The International Fragile X Premutation Registry: building a resource for research and clinical trial readiness

Co‐occurrence of congenital anomalies by maternal race/ethnicity among infants and fetuses with Down syndrome, 2013–2017: A US population‐based analysis

Descriptive analysis of seizures and comorbidities associated with fragile X syndrome

Stephanie L. Sherman Information

University

Position

Professor of Human Genetics School of Medicine

Citations(all)

25357

Citations(since 2020)

6512

Cited By

21445

hIndex(all)

81

hIndex(since 2020)

40

i10Index(all)

221

i10Index(since 2020)

132

Email

University Profile Page

Google Scholar

Stephanie L. Sherman Skills & Research Interests

Down syndrome

Fragile X-associated disorders

Meiosis

Human Genetics

Top articles of Stephanie L. Sherman

Title

Journal

Author(s)

Publication Date

Heritable Variation in Lymphocyte-Related Traits and Risk of Down Syndrome Acute Lymphoblastic Leukemia: A Mendelian Randomization Study

Blood

Yunqi Li

Melissa A Richard

Linda Kachuri

Yao Yu

Ching-Ju Ruu Hsu

...

2023/11/28

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

EBioMedicine

Kathryn Recto

Priyadarshini Kachroo

Tianxiao Huan

David Van Den Berg

Gha Young Lee

...

2023/9/1

Genomic landscape of Down syndrome–associated acute lymphoblastic leukemia

Blood, The Journal of the American Society of Hematology

Zhenhua Li

Ti-Cheng Chang

Jacob J Junco

Meenakshi Devidas

Yizhen Li

...

2023/7/13

Innovating Therapies for Down Syndrome: An International Virtual Conference of the T21 Research Society

Molecular syndromology

Eric D Hamlett

Lisi Flores-Aguilar

Benjamin Handen

Marie-Claude Potier

Ann-Charlotte Granholm

...

2023/4/11

The diagnostic experience of women with fragile X–associated primary ovarian insufficiency (FXPOI)

Journal of Assisted Reproduction and Genetics

Bonnie Poteet

Nadia Ali

Cecelia Bellcross

Stephanie L Sherman

Whitney Espinel

...

2023/1

The International Fragile X Premutation Registry: building a resource for research and clinical trial readiness

Journal of medical genetics

David Hessl

Hilary Rosselot

Robert Miller

Glenda Espinal

Jessica Famula

...

2022/12/1

Co‐occurrence of congenital anomalies by maternal race/ethnicity among infants and fetuses with Down syndrome, 2013–2017: A US population‐based analysis

Birth defects research

Erin B Stallings

Jennifer L Isenburg

Dominique Heinke

Stephanie L Sherman

Russell S Kirby

...

2022/1/15

Descriptive analysis of seizures and comorbidities associated with fragile X syndrome

Molecular genetics & genomic medicine

Igor Albizua

Krista Charen

Lisa Shubeck

Amy Talboy

Elizabeth Berry‐Kravis

...

2022/8

Stephen T. Warren, Ph. D.(1953–2021): A remembrance

The American Journal of Human Genetics

David L Nelson

Janelle Clark

Kathryn Garber

Thomas Glover

Terry Hassold

...

2022/1/6

Identification of PSMB5 as a genetic modifier of fragile X–associated tremor/ataxia syndrome

Proceedings of the National Academy of Sciences

Ha Eun Kong

Junghwa Lim

Alexander Linsalata

Yunhee Kang

Indranil Malik

...

2022/5/31

Differences in Clinical Presentation, Severity, and Treatment of COVID-19 Among Individuals with Down Syndrome from India and High-Income Countries: Data from the Trisomy 21 …

Pinku Halder

Anke Hüls

Patrick T Feany

Nicole T Baumer

Mara Dierssen

...

2022/4/11

COVID-19 vaccination of individuals with Down syndrome—data from the Trisomy 21 Research Society Survey on safety, efficacy, and factors associated with the decision to Be …

Vaccines

Anke Hüls

Patrick T Feany

Sophia Isabella Zisman

Alberto CS Costa

Mara Dierssen

...

2022/3/29

Analyses stratified by maternal age and recombination further characterize genes associated with maternal nondisjunction of chromosome 21

Prenatal Diagnosis

Jonathan M Chernus

Stephanie L Sherman

Eleanor Feingold

2021/4

Spoken language outcome measures for treatment studies in Down syndrome: Feasibility, practice effects, test-retest reliability, and construct validity of variables generated …

Journal of neurodevelopmental disorders

Angela John Thurman

Jamie O Edgin

Stephanie L Sherman

Audra Sterling

Andrea McDuffie

...

2021/12

Refining the risk for fragile X–associated primary ovarian insufficiency (FXPOI) by FMR1 CGG repeat size

Genetics in Medicine

Emily Graves Allen

Krista Charen

Heather S Hipp

Lisa Shubeck

Ashima Amin

...

2021/9/1

Comparison of the Characteristics, Morbidity, and Mortality of COVID-19 and Other Viral and Bacterial Pneumonia in Individuals with Down Syndrome: A Retrospective Cohort Study …

Asúa DRd

M Mayer

MC Ortega

JM Borrel

Bermejo TdJ

...

2021/3/4

COVID-19 in children with Down syndrome: data from the Trisomy 21 Research Society Survey

Journal of clinical medicine

David Emes

Anke Hüls

Nicole Baumer

Mara Dierssen

Shiela Puri

...

2021/10/31

Comparison of COVID-19 and non-COVID-19 pneumonia in Down syndrome

Journal of clinical medicine

Diego Real de Asua

Miguel A Mayer

María del Carmen Ortega

Jose M Borrel

Teresa de Jesús Bermejo

...

2021/8/23

Medical vulnerability of individuals with Down syndrome to severe COVID-19–data from the Trisomy 21 Research Society and the UK ISARIC4C survey

EClinicalMedicine

Anke Hüls

Alberto CS Costa

Mara Dierssen

R Asaad Baksh

Stefania Bargagna

...

2021/3/1

Predictors of Comorbid Conditions in Women Who Carry an FMR1 Premutation

Frontiers in Psychiatry

Emily Graves Allen

Krista Charen

Heather S Hipp

Lisa Shubeck

Ashima Amin

...

2021/10/1

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