Author

Judith F. Knops

Observed names: J F Knops, J Knops, J. Knops, J.F. Knops, Judith Knops

Observed institutions: University of Alabama, Vanderbilt University, LabCorp (United States), University of Alabama at Birmingham, UAB Medicine, Laboratoire de Génétique Médicale, Drexel University

OpenAlex ID: A5111476904

Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia

2005 · K A Kaiser-Rogers, D E McFadden, et al. · Journal of Medical Genetics · 189

PDF

Clonal Selection for Transcriptionally Active Viral Oncogenes during Progression to Cancer

2004 · Brian A. Van Tine, John C. Kappes, et al. · Journal of Virology · 132

Assignment of the human heart tetrodotoxin-resistant voltage-gated Na + channel α-subunit gene (SCN5A) to band 3p21

2008 · A.L. George, Jr., T.A. Varkony, et al. · Cytogenetics and Cell Genetics · 123

Chromosome abnormalities identified in 347 spontaneous abortions collected in Japan

2004 · Masaji Nagaishi, Tatsuo Yamamoto, et al. · Journal of obstetrics and gynaecology research · 110

Prenatal diagnosis of a jumping translocation

2008 · Kendall Annable, Alan E. Donnenfeld, et al. · Prenatal Diagnosis · 73

Terminal deletion of the long arm of chromosome 4 in a mother and two sons

1996 · Maria Descartes, Kim Keppler‐Noreuil, et al. · Clinical Genetics · 30

Morphological and Phenolic Variation in a Three Species Community of Red Oaks

1980 · Judith F. Knops, Richard J. Jensen · Bulletin of the Torrey Botanical Club · 25

Prospective study of 22q11 deletion analysis in fetuses with excess nuchal translucency

2006 · Alan E. Donnenfeld, Denise Cutillo, et al. · American Journal of Obstetrics and Gynecology · 19

In situ analysis of the transcriptional activity of integrated viral DNA using tyramide-FISH.

2001 · B A Van Tine, J Knops, et al. · PubMed · 19

Localization ofHuC(ELAVL3) to Chromosome 19p13.2 by Fluorescencein SituHybridization Utilizing a Novel Tyramide Labeling Technique

1998 · Brian A. Van Tine, Judith F. Knops, et al. · Genomics · 15

Assignment of a Human Voltage-Dependent Sodium Channel α-Subunit Gene (SCN6A) to 2q21-q23

1994 · Alfred L. George, Judith F. Knops, et al. · Genomics · 14

Localization ofHuman elav-like Neuronal Protein 1(Hel-N1) on Chromosome 9p21 by Chromosome Microdissection Polymerase Chain Reaction and Fluorescencein SituHybridization

1996 · Jian Han, Judith F. Knops, et al. · Genomics · 9

Molecular and cytogenetic investigation of complex tissue‐specific duplication and loss of chromosome 21 in a child with a monosomy 21 phenotype

1992 · Natalie Krasikov, Norma Takaesu, et al. · American Journal of Medical Genetics · 7

Journal size increases to four volumes per year Editorial Board additions

2008 · S.D. Wilton, H. Eyre, et al. · Cytogenetics and Cell Genetics · 1

Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocation

2001 · Lori L. Bassett, Ron C. Michaelis, et al. · American Journal of Medical Genetics · 1

Assignment 1 of human MFNG, manic fringe Drosophila homolog, to 22q13.1 using tyramide fluorescence in situ hybridization (T-FISH)

1999 · B.A. van Tine, J. Knops, et al. · Cytogenetic and Genome Research · 1

O45: VUS is not a four-letter word: A better understanding of copy-number variants of unknown significance from examining a large dataset

2026 · Stuart Schwartz, Alexandra Arreola, et al. · Genetics in Medicine Open

P858: Multiple deletions in chromosome 13 mediated by chromothripsis: A case report

2025 · Zach Ou, Judith Knops, et al. · Genetics in Medicine Open

P699: Understanding prenatal chromosomal abnormalities: Importance of both chromosomal and microarray aberrations

2025 · Robert Best, Alexandra Arreola, et al. · Genetics in Medicine Open

PDF

O55: Evaluation of a large cohort of spontaneous pregnancy losses: Intriguing findings from both chromosome and microarray studies

2025 · Stuart Schwartz, Alexandra Arreola, et al. · Genetics in Medicine Open

P592: Cytogenetic and microarray analysis of prenatally detected congenital heart defects (CHD): Diagnostic findings and variation among CHD subtypes

2024 · Stuart Schwartz, Alexandra Arreola, et al. · Genetics in Medicine Open

Dr. John L. Hamerton steps-down from the Associate Editorship

2008 · S.D. Wilton, H. Eyre, et al. · Cytogenetics and Cell Genetics

PDF

Identification of a 1q32.3-q42.1 duplication using chromosome microdissection generated painting probes

1994 · Jilong Han, Judith F. Knops, et al. · The American Journal of Human Genetics

A molecular cytogenetic study of imprinting effect in childhood acute lymphoblastic leukemia with the t(1;19)(q23;p13)

1994 · Judith F. Knops, Jing Han, et al. · The American Journal of Human Genetics

Works count: 24

Citation count: 768

H-index: 11

I10-index: 11