Schulze KV - Search Results

1

Novel parent-of-origin-specific differentially methylated loci on chromosome 16.

Schulze KV, Szafranski P, Lesmana H, Hopkin RJ, Hamvas A, Wambach JA, Shinawi M, Zapata G, Carvalho CMB, Liu Q, Karolak JA, Lupski JR, Hanchard NA, Stankiewicz P. Schulze KV, et al. Clin Epigenetics. 2019 Apr 8;11(1):60. doi: 10.1186/s13148-019-0655-8. Clin Epigenetics. 2019. PMID: 30961659 Free PMC article.

2

Aberrant DNA methylation as a diagnostic biomarker of diabetic embryopathy.

Schulze KV, Bhatt A, Azamian MS, Sundgren NC, Zapata GE, Hernandez P, Fox K, Kaiser JR, Belmont JW, Hanchard NA. Schulze KV, et al. Genet Med. 2019 Nov;21(11):2453-2461. doi: 10.1038/s41436-019-0516-z. Epub 2019 Apr 17. Genet Med. 2019. PMID: 30992551 Free article.

3

Edematous severe acute malnutrition is characterized by hypomethylation of DNA.

Schulze KV, Swaminathan S, Howell S, Jajoo A, Lie NC, Brown O, Sadat R, Hall N, Zhao L, Marshall K, May T, Reid ME, Taylor-Bryan C, Wang X, Belmont JW, Guan Y, Manary MJ, Trehan I, McKenzie CA, Hanchard NA. Schulze KV, et al. Nat Commun. 2019 Dec 19;10(1):5791. doi: 10.1038/s41467-019-13433-6. Nat Commun. 2019. PMID: 31857576 Free PMC article.

4

Biases in arginine codon usage correlate with genetic disease risk.

Schulze KV, Hanchard NA, Wangler MF. Schulze KV, et al. Genet Med. 2020 Aug;22(8):1407-1412. doi: 10.1038/s41436-020-0813-6. Epub 2020 May 6. Genet Med. 2020. PMID: 32371920 Free article.

5

Detection of low-level parental somatic mosaicism for clinically relevant SNVs and indels identified in a large exome sequencing dataset.

Domogala DD, Gambin T, Zemet R, Wu CW, Schulze KV, Yang Y, Wilson TA, Machol I, Liu P, Stankiewicz P. Domogala DD, et al. Among authors: schulze kv. Hum Genomics. 2021 Dec 20;15(1):72. doi: 10.1186/s40246-021-00369-6. Hum Genomics. 2021. PMID: 34930489 Free PMC article.

6

Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traits.

Yuan B, Schulze KV, Assia Batzir N, Sinson J, Dai H, Zhu W, Bocanegra F, Fong CT, Holder J, Nguyen J, Schaaf CP, Yang Y, Bi W, Eng C, Shaw C, Lupski JR, Liu P. Yuan B, et al. Among authors: schulze kv. Genome Med. 2022 Sep 30;14(1):113. doi: 10.1186/s13073-022-01113-y. Genome Med. 2022. PMID: 36180924 Free PMC article.

7

A first-generation genome-wide map of correlated DNA methylation demonstrates highly coordinated and tissue-independent clustering across regulatory regions.

Jajoo A, Hirschi O, Schulze K, Guan Y, Hanchard NA. Jajoo A, et al. Res Sq [Preprint]. 2023 May 15:rs.3.rs-2852818. doi: 10.21203/rs.3.rs-2852818/v1. Res Sq. 2023. PMID: 37333260 Free PMC article. Preprint.

8

Genetic Variants in Carbohydrate Digestive Enzyme and Transport Genes Associated with Risk of Irritable Bowel Syndrome.

Hong H, Schulze KV, Copeland IE, Atyam M, Kamp K, Hanchard NA, Belmont J, Ringel-Kulka T, Heitkemper M, Shulman RJ. Hong H, et al. Among authors: schulze kv. medRxiv [Preprint]. 2023 Sep 22:2023.09.20.23295800. doi: 10.1101/2023.09.20.23295800. medRxiv. 2023. PMID: 37790351 Free PMC article. Preprint.

9

Detection of Clinically Relevant Monogenic Copy-Number Variants by a Comprehensive Genome-Wide Microarray with Exonic Coverage.

Chau MHK, Anderson SA, Song R, Cooper L, Ward PA, Yuan B, Shaw C, Stankiewicz P, Cheung SW, Vossaert L, Wang Y, Owen NM, Smith J, Bacino CA, Schulze KV, Bi W. Chau MHK, et al. Among authors: schulze kv. Clin Chem. 2025 Jan 3;71(1):141-154. doi: 10.1093/clinchem/hvae188. Clin Chem. 2025. PMID: 39749505

10

Clinical characterization of individuals with the distal 1q21.1 microdeletion.

Edwards SD, Schulze KV, Rosenfeld JA, Westerfield LE, Gerard A, Yuan B, Grigorenko EL, Posey JE, Bi W, Liu P. Edwards SD, et al. Among authors: schulze kv. Am J Med Genet A. 2021 May;185(5):1388-1398. doi: 10.1002/ajmg.a.62104. Epub 2021 Feb 11. Am J Med Genet A. 2021. PMID: 33576134

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