LawrenceC.LaymanMD

PubMed

• Heterozygous ZNHIT3 variants within the 17q12 recurrent deletion region are associated with Mayer-Rokitansky-Kuster Hauser (MRKH) syndrome.
  Quansheng Du, Lynn P Chorich, Zoe A Hawkins, Megan E Sullivan, Eun Kyung Ko, Hyung-Goo Kim, James Knight, Michael Friez, John A Phillips 3rd, Soumia Brakta, Hugh S Tay...> ;Molecular and Cellular Endocrinology. 2024 Apr 8
• Prevalence of pathogenic variants and digenic disease in patients diagnosed with normosmic hypogonadotropic hypogonadism/Kallmann Syndrome.
  Robert A Roman, Lynn Chorich, Zoe Hawkins, Soo-Hyun Kim, Hyung-Goo Kim, Alexandra Poch, Michael P Dougherty, Lawrence C Layman> ;Molecular and Cellular Endocrinology. 2024 Apr 7
• 1 citations
  Endogenous estradiol contributes to vascular endothelial dysfunction in premenopausal women with type 1 diabetes.
  Abigayle B Simon, Cassandra C Derella, Marsha Blackburn, Jeffrey Thomas, Lawrence C Layman, Matthew S Nicholson, Jennifer Waller, Ahmed Elmarakby, Karim M Saad, Ryan A...> ;Cardiovascular Diabetology. 2023 Sep 7
• 1 citations
  Coordination of canonical and noncanonical Hedgehog signalling pathways mediated by WDR11 during primordial germ cell development.
  Jiyoung Lee, Yeonjoo Kim, Paris Ataliotis, Hyung-Goo Kim, Dae-Won Kim, Dorothy C Bennett, Nigel A Brown, Lawrence C Layman, Soo-Hyun Kim> ;Scientific Reports. 2023 Jul 29
• Investigation of subfertility in the female Nsmf knockout mouse.
  Erica D Louden, Michael P Dougherty, Lynn P Chorich, Ali Eroglu, Lawrence C Layman> ;F&S Science. 2023 Nov 1
• 8 citations
  Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic Testing.
  Nikhil S Sahajpal, Ashis K Mondal, Timothy Fee, Benjamin Hilton, Alex R Hastie, Alka Chaubey, Barbara R DuPont, Ravindra Kolhe, Layman, L.> ;The Journal of Molecular Diagnostics. 2023 Apr 1
• 2 citations
  Rare structural variants, aneuploidies, and mosaicism in individuals with Mullerian aplasia detected by optical genome mapping.
  Soumia Brakta, Zoe A Hawkins, Nikhil Sahajpal, Natalie Seman, Dina Kira, Lynn P Chorich, Hyung-Goo Kim, Hongyan Xu, John A Phillips 3rd, Ravindra Kolhe, Layman, L.> ;Human Genetics. 2023 Apr 1
• Adolescent With Concomitant Transverse and Longitudinal Vaginal Septa.
  Kyler Perry, Sherita A King, Christine Callaway, Larisa Gavrilova-Jordan, Lawrence Layman, Jeffrey Donohoe> ;Urology. 2023 Apr 1
• 1 citations
  Identification of two novel autism genes,and, in Qatar simplex families through exome sequencing.
  Vijay Gupta, Afif Ben-Mahmoud, Bonsu Ku, Dinesh Velayutham, Zainab Jan, Abdi Yousef Aden, Ahmad Kubbar, Fouad Alshaban, Lawrence W Stanton, Puthen Veettil Jithesh, Hyu...> ;Frontiers in Psychiatry. 2023 Jan 1
• 2 citations
  Optical Genome Mapping and Single Nucleotide Polymorphism Microarray: An Integrated Approach for Investigating Products of Conception.
  Sahajpal, N., Mondal, A., Ananth, S., Pundkar, C., Jones, K., Williams, C., Fee, T., Weissman, A., Tripodi, G., Oza, E., Gavrilova-Jordan, L., Omar, N., Hastie, A., Du...> ;Genes. 2022 Apr 3
• 4 citations
  A rigorousgenomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders.
  Ben-Mahmoud, A., Jun, K., Gupta, V., Shastri, P., de la Fuente, A., Park, Y., Shin, K., Kim, C., da Cruz, A., Pinto, I., Minasi, L., Silva da Cruz, A., Faivre, L., Cal...> ;Frontiers in Molecular Neuroscience. 2022 Jan 1
• 11 citations
  Genetics of hypogonadotropic Hypogonadism-Human and mouse genes, inheritance, oligogenicity, and genetic counseling.
  Erica Louden, Alexandra Poch, Hyung-Goo Kim, Afif Ben-Mahmoud, Soo-Hyun Kim, Lawrence C. Layman> ;Molecular and Cellular Endocrinology. 2021 Aug 20
• Twenty-year follow-up of the facial phenotype of Brazilian patients with Sotos syndrome.
  Matheus Augusto Araujo Castro, Juliana Heather Vedovato dos Santos, Rachel Sayuri Honjo, Guilherme L. Yamamoto, Débora Romeo Bertola, Anna C.E. Hurst, Lynn P. Chorich,...> ;American Journal of Medical Genetics. Part A. 2021 Aug 18
• 13 citations
  Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer–Rokitansky–Küster–Hauser Syndrome
  Sasha Mikhael, Sonal Dugar, Madison Morton, Lynn P. Chorich, Kerlene Berwick Tam, Amy C. Lossie, Hyung-Goo Kim, James R. Knight, Hugh S. Taylor, Souhrid Mukherjee, Joh...> ;Human Genetics. 2021 Jan 19
• 8 citations
  Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.
  Julia Doll, Barbara Vona, Linda Schnapp, Franz Rüschendorf, Imran Khan, Saadullah Khan, Noor Muhammad, Sher Alam Khan, Hamed Nawaz, Ajmal Khan, Naseer Ahmad, Susanne M...> ;Genes. 2020 Nov 11
• Would combined glucocorticoid and gonadotropin therapy improve pregnancy rates in women with primary ovarian insufficiency
  Lawrence C. Layman> ;F&S Reports. 2020 Oct 22
• 12 citations
  Comparative Genomic Mapping Implicates LRRK2 for Intellectual Disability and Autism at 12q12, and HDHD1, as Well as PNPLA4, for X-Linked Intellectual Disability at Xp2...
  Jonathan D J Labonne, Terri M. Driessen, Marvin E Harris, Il-Keun Kong, Soumia Brakta, John Graham Theisen, Modibo Sangare, Lawrence C. Layman, Cheol-Hee Kim, Janghoo ...> ;Journal of Clinical Medicine. 2020 Jan 19
• 15 citations
  The Use of Whole Exome Sequencing in a Cohort of Transgender Individuals to Identify Rare Genetic Variants.
  J. Graham Theisen, Viji Sundaram, Mary S. Filchak, Lynn P. Chorich, Megan E. Sullivan, James R. Knight, Hyung-Goo Kim, Lawrence C. Layman> ;Scientific Reports. 2019 Dec 27
• 25 citations
  Disruption of PHF21A causes syndromic intellectual disability with craniofacial anomalies, epilepsy, hypotonia, and neurobehavioral problems including autism
  Hyung-Goo Kim, Jill A. Rosenfeld, Daryl A. Scott, Gerard Bénédicte, Jonathan D J Labonne, Jason Brown, Marianne McGuire, Sonal Mahida, Sakkubai Naidu, Jacqueline Gutie...> ;Molecular Autism. 2019 Oct 22
• 4 citations
  Academic pursuits in board-certified reproductive endocrinologists
  Lawrence C. Layman, Eve C. Feinberg, Bradley S. Hurst, Scott J. Morin, Jamie L Morris, Margareta D. Pisarska, Yolanda R. Smith, Thomas M Price> ;Fertility and Sterility. 2018 Sep 1
• 9 citations
  Copy number variation and regions of homozygosity analysis in patients with MÜLLERIAN aplasia
  Durkadin Demir Eksi, Yiping Shen, Munire Erman, Lynn P. Chorich, Megan E. Sullivan, Meric Bilekdemir, Elanur Yilmaz, Guven Luleci, Hyung Goo Kim, Özgül M. Alper, Lawre...> ;Molecular Cytogenetics. 2018 Feb 3
• 7 citations
  JAK/STAT signaling pathway gene expression is reduced following Nelf knockdown in GnRH neurons
  Eunkyung Ko, Lynn P. Chorich, Megan E. Sullivan, Richard S. Cameron, Lawrence C. Layman> ;Molecular and Cellular Endocrinology. 2017 Oct 16
• 6 citations
  Berberine Inhibits Uterine Leiomyoma Cell Proliferation via Downregulation of Cyclooxygenase 2 and Pituitary Tumor-Transforming Gene 1.
  Tung Yueh Chuang, Jie Min, Hsiao Li Wu, Cristina McCrary, Michael P. Diamond, Ricardo Azziz, Ayman Al-Hendy, Yen Hao Chen> ;Reproductive Sciences. 2017 Jul 1
• 29 citations
  Genetic analysis of Mayer-Rokitansky-Kuster-Hauser syndrome in a large cohort of families.
  Lacey S. Williams, Durkadin Demir Eksi, Yiping Shen, Amy C. Lossie, Lynn P. Chorich, Megan E. Sullivan, John A. Phillips, Munire Erman, Hyung Goo Kim, Özgül M. Alper, ...> ;Fertility and Sterility. 2017 Jul 1
• 7 citations
  Genetic basis of eugonadal and hypogonadal female reproductive disorders.
  Tatiana Trofimova, Daria Lizneva, Larisa Suturina, Walidah Walker, Yen Hao Chen, Ricardo Azziz, Lawrence C. Layman> ;Best Practice & Research. Clinical Obstetrics & Gynaecology. 2017 May 9
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