David H. Ledbetter - Publications, H-index & Citations

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David H. Ledbetter

King Khalid University Hospital

112H-index

493Paper Count

5.8WCitation Count

Published Papers 135

Publication Date

Transforming Prenatal Care in a Highly Inbred Population: Impact of a Multidisciplinary Board

Prenatal Diagnosis

IF2.7

2026-05-01

PREAI

Alfalah, Abdullah H.; Alzaidan, Hamad; Alfares, Ahmed; Sulaiman, Raashda; Alharbi, Hana; Al-Hamed, Mohamed H.; Albanyan, Saleh; Ledbetter, David H.; Alqahtani, Yara; Aljanfawi, Wafa; Tohary, Mohammed; AlHabib, Lamees; Alakeel, Hajar; AlShammari, Randa; Alwazae, Meshari M.; Alqasir, Ibrahim; Kurdi, Wesam; Tulbah, Maha; Almass, Rawan; Alturki, Fatimah; Almutairi, Gawaher; Imtiaz, Faiqa; Al-Owain, Mohammed

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Testing the performance of polygenic scores for multiple traits to explain cerebral palsy in two independent cohorts

eBioMedicine

IF10.8

2026-03-14

OAAI

Jodi T. Thomas; Alexander S.F. Berry; Matthew T. Oetjens; Jesia G. Berry; Alastair H. MacLennan; Scott D. Gordon; Andrew T. Hale; Catherine M. Olsen; David C. Whiteman; Rebecca I. Torene; David H. Ledbetter; Nicholas G. Martin; Clare L. van Eyk; Jozef Gecz; Scott M. Myers; Brittany L. Mitchell; Mark A. Corbett

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Advancing Mental Health Research Through Strategic Integration of Transdiagnostic Dimensions and Genomics

BIOLOGICAL PSYCHIATRY

IF9

2025-03-01

PREAI

Doyle, Alysa E.; Bearden, Carrie E.; Gur, Raquel E.; Ledbetter, David H.; Martin, Christa L.; McCoy Jr, Thomas H.; Pasaniuc, Bogdan; Perlis, Roy H.; Smoller, Jordan W.; Davis, Lea K.

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A genome-first study of sex chromosome aneuploidies provides evidence of Y chromosome dosage effects on autism risk

NATURE COMMUNICATIONS

IF15.7

2024-10-15

OAAI

Berry, Alexander S. F.; Finucane, Brenda M.; Myers, Scott M.; Walsh, Lauren K.; Seibert, John M.; Martin, Christa Lese; Ledbetter, David H.; Oetjens, Matthew T.

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Systematic analysis of variants escaping nonsense-mediated decay uncovers candidate Mendelian diseases

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2024-01-01

OAAI

Torene, Rebecca I.; Sacoto, Maria J. Guillen; Millan, Francisca; Zhang, Zhancheng; Mcgee, Stephen; Oetjens, Matthew; Heise, Elizabeth; Chong, Karen; Sidlow, Richard; O'Grady, Lauren; Sahai, Inderneel; Martin, Christa L.; Ledbetter, David H.; Myers, Scott M.; Mitchell, Kevin J.; Retterer, Kyle

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Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing Guidelines: A Systematic Review and Meta-analysis

OBSTETRICAL & GYNECOLOGICAL SURVEY

IF3.6

2023-11-01

PREAI

Gonzalez-Mantilla, P. J.; Hu, Y.; Myers, S. M.; Finucane, B. M.; Ledbetter, D. H.; Martin, C. L.; Moreno-De-Luca, A.

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A novel application of spectrograms with machine learning can detect patient ventilator dyssynchrony

BIOMEDICAL SIGNAL PROCESSING AND CONTROL

IF4.9

2023-09-01

OAAI

Obeso, Ishmael; Yoon, Benjamin; Ledbetter, David; Aczon, Melissa; Laksana, Eugene; Zhou, Alice; Eckberg, R. Andrew; Mertan, Keith; Khemani, Robinder G.; Wetzel, Randall

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Diagnostic Yield of Exome Sequencing in Cerebral Palsy and Implications for Genetic Testing Guidelines A Systematic Review and Meta-analysis

JAMA PEDIATRICS

IF18

2023-05-01

PREAI

Gonzalez-Mantilla, Pedro J.; Hu, Yirui; Myers, Scott M.; Finucane, Brenda M.; Ledbetter, David H.; Martin, Christa L.; Moreno-De-Luca, Andres

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Untitled

AUTISM RESEARCH

IF5.6

2023-04-22

PREAI

Finucane, Brenda; Myers, Scott M.; Challman, Thomas D.; Martin, Christa Lese; Ledbetter, David H.

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Association of Supernumerary Sex Chromosome Aneuploidies With Venous Thromboembolism

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

IF55

2023-01-17

OAAI

Berry, Alexander S. F.; Finucane, Brenda M.; Myers, Scott M.; Abril, Angela; Kirchner, H. Lester; Ledbetter, David H.; Martin, Christa Lese; Oetjens, Matthew T.

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BRIEF REPORT Phenotypic shift in copy number variants: Evidence in 16p11.2 duplication syndrome

GENETICS IN MEDICINE

IF6.2

2023-01-01

OAAI

Taylor, Cora M.; Finucane, Brenda M.; Moreno-De-Luca, Andres; Walsh, Lauren K.; Martin, Christa Lese; Ledbetter, David H.

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Prevalence and Penetrance of Rare Pathogenic Variants in Neurodevelopmental Psychiatric Genes in a Health Care System Population

AMERICAN JOURNAL OF PSYCHIATRY

IF14.7

2023-01-01

OAAI

Shimelis, Hermela; Oetjens, Matthew T.; Walsh, Lauren K.; Wain, Karen E.; Znidarsic, Masa; Myers, Scott M.; Finucane, Brenda M.; Ledbetter, David H.; Martin, Christa Lese

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Frequency of truncating FLCN variants and Birt-Hogg-Dube-associated phenotypes in a health care system population

GENETICS IN MEDICINE

IF6.2

2022-09-01

OAAI

Savatt, Juliann M.; Shimelis, Hermela; Moreno-De-Luca, Andres; Strande, Natasha T.; Oetjens, Matthew T.; Ledbetter, David H.; Martin, Christa Lese; Myers, Scott M.; Finucane, Brenda M.

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Medical manifestations and health care utilization among adult MyCode participants with neurodevelopmental psychiatric copy number variants

GENETICS IN MEDICINE

IF6.2

2022-03-01

OAAI

Finucane, Brenda; Oetjens, Matthew T.; Johns, Alicia; Myers, Scott M.; Fisher, Ciaran; Habegger, Lukas; Maxwell, Evan K.; Reid, Jeffrey G.; Ledbetter, David H.; Kirchner, H. Lester; Martin, Christa Lese

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Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology

AMERICAN JOURNAL OF PSYCHIATRY

IF14.7

2022-03-01

OAAI

Jacquemont, Sebastien; Huguet, Guillaume; Klein, Marieke; Chawner, Samuel J. R. A.; Donald, Kirsten A.; van den Bree, Marianne B. M.; Sebat, Jonathan; Ledbetter, David H.; Constantino, John N.; Earl, Rachel K.; McDonald-McGinn, Donna M.; van Amelsvoort, Therese; Swillen, Ann; O'Donnell-Luria, Anne H.; Glahn, David C.; Almasy, Laura; Eichler, Evan E.; Scherer, Stephen W.; Robinson, Elise; Bassett, Anne S.; Martin, Christa Lese; Finucane, Brenda; Vorstman, Jacob A. S.; Bearden, Carrie E.; Gur, Raquel E.

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Early cancer diagnoses through BRCA1/2 screening of unselected adult biobank participants (vol 20, pg 554, 2018)

GENETICS IN MEDICINE

IF6.2

2021-12-01

OAAI

Buchanan, Adam H.; Manickam, Kandamurugu; Meyer, Michelle N.; Wagner, Jennifer K.; Hallquist, Miranda L. G.; Williams, Janet L.; Rahm, Alanna Kulchak; Williams, Marc S.; Chen, Zong-Ming E.; Shah, Chaitali K.; Garg, Tullika K.; Lazzeri, Amanda L.; Schwartz, Marci L. B.; Lindbuchler, D' Andra M.; Fan, Audrey L.; Leeming, Rosemary; Servano, Pedro O., III; Smith, Ashlee L.; Vogel, Victor G.; Abul-Husn, Noura S.; Dewey, Frederick E.; Lebo, Matthew S.; Mason-Suares, Heather M.; Ritchie, Marylyn D.; Davis, F. Daniel; Carey, David J.; Feinberg, David T.; Faucett, W. Andrew; Ledbetter, David H.; Murray, Michael F.

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DELETERIOUS SHIFT IN FUNCTIONAL PERFORMANCE EXPLAINS CLINICAL VARIABILITY IN RARE GENETIC NEURODEVELOPMENTAL PSYCHIATRIC DISORDERS

EUROPEAN NEUROPSYCHOPHARMACOLOGY

IF6.7

2021-10-01

PREAI

Ledbetter, David; Finucane, Brenda; Taylor, Cora; de Luca, Andres Morena; Myers, Scott; Martin, Christa

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Recontacting registry participants with genetic updates through GenomeConnect, the ClinGen patient registry

GENETICS IN MEDICINE

IF6.2

2021-09-01

OAAI

Savatt, Juliann M.; Azzariti, Danielle R.; Ledbetter, David H.; Palen, Emily; Rehm, Heidi L.; Riggs, Erin Rooney; Martin, Christa Lese

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Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy

OBSTETRICAL & GYNECOLOGICAL SURVEY

IF3.6

2021-07-01

PREAI

Moreno-De-Luca, Andres; Millan, Francisca; Pesacreta, Denis R.; Elloumi, Houda Z.; Oetjens, Matthew T.; Teigen, Claire; Wain, Karen E.; Scuffins, Julie; Myers, Scott M.; Torene, Rebecca I.; Gainullin, Vladimir G.; Arvai, Kevin; Kirchner, H. Lester; Ledbetter, David H.; Retterer, Kyle; Martin, Christa L.

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Diagnostic genetic testing for neurodevelopmental psychiatric disorders: closing the gap between recommendation and clinical implementation

CURRENT OPINION IN GENETICS & DEVELOPMENT

IF3.6

2021-06-01

OAAI

Finucane, Brenda M.; Ledbetter, David H.; Vorstman, Jacob A. S.

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Research Directions