Andy Drackley

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 20

Top Topics

Photodynamic Therapy

Peripheral Nerve

Mitochondrial Dna

Top Venues

American journal of medical genetics. Part A

American journal of medical genetics. Part C, Seminars in medical genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Sharon H Zhao, Kai Lee Yap, Valerie Allegretti, Andy Drackley, Alexander Ing, Adam Gordon, Andrew Skol, Patrick McMullen, Brenda L Bohnsack, Sudhi P Kurup, Hantamalala Ralay Ranaivo, Jennifer L Rossen
A Case of Non-Syndromic Congenital Cataracts Caused by a Novel MAF Variant in the C-Terminal DNA-Binding Domain-Case Report and Literature Review. Genes 15 (6) (2024)
Sharon H Zhao, Kai Lee Yap, Valerie Allegretti, Andy Drackley, Alexander Ing, Adam Gordon, Andrew Skol, Patrick McMullen, Brenda L Bohnsack, Sudhi P Kurup, Hantamalala Ralay Ranaivo, Jennifer L Rossen
A Case of Non-Syndromic Congenital Cataracts Caused by a Novel MAF Variant in the C-Terminal DNA-Binding Domain-Case Report and Literature Review. Genes 15 (6) (2024)
Kunal Kanwar, Saffiya Bashey, Brenda L Bohnsack, Andy Drackley, Alexander Ing, Safa Rahmani, Hantamalala Ralay Ranaivo, Patrick McMullen, Andrew Skol, Kailee Yap, Valerie Allegretti, Jennifer L Rossen
Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysis. American journal of medical genetics. Part A (2024)
Kunal Kanwar, Saffiya Bashey, Brenda L Bohnsack, Andy Drackley, Alexander Ing, Safa Rahmani, Hantamalala Ralay Ranaivo, Patrick McMullen, Andrew Skol, Kailee Yap, Valerie Allegretti, Jennifer L Rossen
Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysis. American journal of medical genetics. Part A 194 (8) (2024)
Andy Drackley, Merlene Peter, Pamela Rathbun, Alexander Ing, Carlos E Prada, Kai Lee Yap
Homozygosity for disease-causing variants in AMT and GLDC in a patient with severe nonketotic hyperglycinemia. American journal of medical genetics. Part A 194 (8) (2024)
Kunal Kanwar, Saffiya Bashey, Brenda L Bohnsack, Andy Drackley, Alexander Ing, Safa Rahmani, Hantamalala Ralay Ranaivo, Patrick McMullen, Andrew Skol, Kailee Yap, Valerie Allegretti, Jennifer L Rossen
Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysis. American journal of medical genetics. Part A 194 (8) (2024)
Andy Drackley, Merlene Peter, Pamela Rathbun, Alexander Ing, Carlos E Prada, Kai Lee Yap
Homozygosity for disease-causing variants in AMT and GLDC in a patient with severe nonketotic hyperglycinemia. American journal of medical genetics. Part A 194 (8) (2024)
Jenny P Garzon, Andrea Patete, Lindsey Aschbacher-Smith, Dima Qu'd, Geraldine Kelly-Mancuso, Carolyn R Serbinski, Allison Goetsch Weisman, Madison Hankins, Michael Sawin, Katherine Kim, Andy Drackley, Janice Zeid, K Nicole Weaver, Robert J Hopkin, Howard M Saal, Joel Charrow, Elizabeth Schorry, Robert Listernick, Brittany N Simpson, Carlos E Prada
Expanding the phenotype of neurofibromatosis type 1 microdeletion syndrome. American journal of medical genetics. Part C, Seminars in medical genetics (2024)
Andy Drackley, Merlene Peter, Pamela Rathbun, Alexander Ing, Carlos E Prada, Kai Lee Yap
Homozygosity for disease-causing variants in AMT and GLDC in a patient with severe nonketotic hyperglycinemia. American journal of medical genetics. Part A (2024)
Andy Drackley, Merlene Peter, Pamela Rathbun, Alexander Ing, Carlos E Prada, Kai Lee Yap
Homozygosity for disease-causing variants in AMT and GLDC in a patient with severe nonketotic hyperglycinemia. American journal of medical genetics. Part A 194 (8) (2024)
Anne M McRae, Jaime Duncan, Andy Drackley, Alexander Ing, Valerie Allegretti, Carolyn R Serbinski, Angelique Mercier, Carlos E Prada, Sarah Jurgensmeyer
Further Delineation of the Proximal 16p11.2 Microdeletion Syndrome: Novel Findings Among 22 New Individuals. American journal of medical genetics. Part A (2024)
Sharon H Zhao, Kai Lee Yap, Valerie Allegretti, Andy Drackley, Alexander Ing, Adam Gordon, Andrew Skol, Patrick McMullen, Brenda L Bohnsack, Sudhi P Kurup, Hantamalala Ralay Ranaivo, Jennifer L Rossen
A Case of Non-Syndromic Congenital Cataracts Caused by a Novel MAF Variant in the C-Terminal DNA-Binding Domain-Case Report and Literature Review. Genes 15 (6) (2024)
Andy Drackley, Lenika De Simone, Nancy L Kuntz, Safa Rahmani, Alexander Ing, Vamshi K Rao, Pamela Rathbun, Kai Lee Yap
Expansion of the phenotypic spectrum associated with pathogenic missense variation in DHX16. American journal of medical genetics. Part A (2023)
Kyle S Chan, Brenda L Bohnsack, Alexander Ing, Andy Drackley, Valerie Castelluccio, Kevin X Zhang, Hanta Ralay-Ranaivo, Jennifer L Rossen
Diagnostic Yield of Genetic Testing for Ocular and Oculocutaneous Albinism in a Diverse United States Pediatric Population. Genes 14 (1) (2023)
Kyle S Chan, Brenda L Bohnsack, Alexander Ing, Andy Drackley, Valerie Castelluccio, Kevin X Zhang, Hanta Ralay-Ranaivo, Jennifer L Rossen
Diagnostic Yield of Genetic Testing for Ocular and Oculocutaneous Albinism in a Diverse United States Pediatric Population. Genes 14 (1) (2023)
Jennifer L Rossen, Brenda L Bohnsack, Kevin X Zhang, Alexander Ing, Andy Drackley, Valerie Castelluccio, Hanta Ralay-Ranaivo
Evaluation of Genetic Testing in a Cohort of Diverse Pediatric Patients in the United States with Congenital Cataracts. Genes 14 (3) (2023)
Jennifer L Rossen, Brenda L Bohnsack, Kevin X Zhang, Alexander Ing, Andy Drackley, Valerie Castelluccio, Hanta Ralay-Ranaivo
Evaluation of Genetic Testing in a Cohort of Diverse Pediatric Patients in the United States with Congenital Cataracts. Genes 14 (3) (2023)
Kyle S Chan, Brenda L Bohnsack, Alexander Ing, Andy Drackley, Valerie Castelluccio, Kevin X Zhang, Hanta Ralay-Ranaivo, Jennifer L Rossen
Diagnostic Yield of Genetic Testing for Ocular and Oculocutaneous Albinism in a Diverse United States Pediatric Population. Genes 14 (1) (2023)
Jennifer L Rossen, Brenda L Bohnsack, Kevin X Zhang, Alexander Ing, Andy Drackley, Valerie Castelluccio, Hanta Ralay-Ranaivo
Evaluation of Genetic Testing in a Cohort of Diverse Pediatric Patients in the United States with Congenital Cataracts. Genes 14 (3) (2023)
Kyle S Chan, Brenda L Bohnsack, Alexander Ing, Andy Drackley, Valerie Castelluccio, Kevin X Zhang, Hanta Ralay-Ranaivo, Jennifer L Rossen
Diagnostic Yield of Genetic Testing for Ocular and Oculocutaneous Albinism in a Diverse United States Pediatric Population. Genes 14 (1) (2023)