Alexander Ing

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 20

Top Topics

Knee Osteoarthritis

Photodynamic Therapy

Mitochondrial Dna

Top Venues

American journal of medical genetics. Part A

Cold Spring Harbor molecular case studies

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)
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)
Alexander Ing, Alissa Wlodaver, Dawn Kirschmann, Erica Toledo, Christopher McCabe, Sabah Kadri, Mary Kate McIntyre, Joanne Salazar, Kristina Firestein, Joel Charrow, Victoria Sanders, Theresa A Laguna, Kai Lee Yap
Transcript analysis for variant classification resolution in a child with primary ciliary dyskinesia. Cold Spring Harbor molecular case studies 7 (1) (2021)