Lawrence C. Layman

2.9k total citations
54 papers, 1.8k citations indexed

About

Lawrence C. Layman is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Lawrence C. Layman has authored 54 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 29 papers in Molecular Biology and 17 papers in Reproductive Medicine. Recurrent topics in Lawrence C. Layman's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Sexual Differentiation and Disorders (12 papers) and Hypothalamic control of reproductive hormones (12 papers). Lawrence C. Layman is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (21 papers), Sexual Differentiation and Disorders (12 papers) and Hypothalamic control of reproductive hormones (12 papers). Lawrence C. Layman collaborates with scholars based in United States, South Korea and Qatar. Lawrence C. Layman's co-authors include Hyung‐Goo Kim, Paul G. McDonough, Yiping Shen, Ricardo Azziz, Sandra P.T. Tho, Richard H. Reindollar, Lynn P. Chorich, Saleh Heneidi, Yen-Hao Chen and Gregorio D. Chazenbalk and has published in prestigious journals such as New England Journal of Medicine, The Journal of Clinical Endocrinology & Metabolism and Diabetes.

In The Last Decade

Lawrence C. Layman

51 papers receiving 1.6k citations

Peers

Lawrence C. Layman

GENET

PHEOH

Virpi Töhönen Sweden

Lawrence C. Layman United States

Céline J. Guigon France

JoAnne S. Richards United States

Constance Chen United States

Yugong Ho United States

Albert de la Chapelle Finland

Kenshiro Hara Japan

Jean‐Pierre Siffroi France

Yoshikatsu Uematsu Japan

Virpi Töhönen Sweden

Lawrence C. Layman

445 ×0.5

GENET

980 ×1.2

257 ×0.4

312 ×0.9

PHEOH

106 ×0.5

Citations per year, relative to Lawrence C. Layman Lawrence C. Layman (= 1×) peers Virpi Töhönen

Countries citing papers authored by Lawrence C. Layman

Since Specialization

Citations

This map shows the geographic impact of Lawrence C. Layman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Lawrence C. Layman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lawrence C. Layman more than expected).

Fields of papers citing papers by Lawrence C. Layman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lawrence C. Layman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Lawrence C. Layman. The network helps show where Lawrence C. Layman may publish in the future.

Co-authorship network of co-authors of Lawrence C. Layman

This figure shows the co-authorship network connecting the top 25 collaborators of Lawrence C. Layman. A scholar is included among the top collaborators of Lawrence C. Layman based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Lawrence C. Layman. Lawrence C. Layman is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Kishikawa, Shotaro, Vijay Gupta, Natalia T. Leach, et al.. (2023). A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome. Scientific Reports. 13(1). 12984–12984. 2 indexed citations

Lee, Jiyoung, Yeon-Joo Kim, Paris Ataliotis, et al.. (2023). Coordination of canonical and noncanonical Hedgehog signalling pathways mediated by WDR11 during primordial germ cell development. Scientific Reports. 13(1). 12309–12309. 3 indexed citations

Labonne, Jonathan D. J., Terri M. Driessen, Il‐Keun Kong, et al.. (2020). Comparative Genomic Mapping Implicates LRRK2 for Intellectual Disability and Autism at 12q12, and HDHD1, as Well as PNPLA4, for X-Linked Intellectual Disability at Xp22.31. Journal of Clinical Medicine. 9(1). 274–274. 18 indexed citations

Osborn, Daniel P. S., Ji‐Young Lee, Masatake Araki, et al.. (2017). WDR11‐mediated Hedgehog signalling defects underlie a new ciliopathy related to Kallmann syndrome. EMBO Reports. 19(2). 269–289. 40 indexed citations

Quaynor, Samuel D., Soo‐Hyun Kim, Hyung‐Goo Kim, et al.. (2016). Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome. Molecular and Cellular Endocrinology. 437. 86–96. 54 indexed citations

Labonne, Jonathan D. J., Yiping Shen, Il‐Keun Kong, et al.. (2016). Comparative deletion mapping at 1p31.3-p32.2 implies NFIA responsible for intellectual disability coupled with macrocephaly and the presence of several other genes for syndromic intellectual disability. Molecular Cytogenetics. 9(1). 24–24. 26 indexed citations

Labonne, Jonathan D. J., Julie R. Jones, Priya Anand, et al.. (2015). Concomitant partial exon skipping by a unique missense mutation of RPS6KA3 causes Coffin–Lowry syndrome. Gene. 575(1). 42–47. 8 indexed citations

Nguyen, Lam Son, Hyung‐Goo Kim, Jill A. Rosenfeld, et al.. (2013). Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders. Human Molecular Genetics. 22(9). 1816–1825. 116 indexed citations

Kim, Hyung‐Goo, et al.. (2013). Identification of HESX1 mutations in Kallmann syndrome. Fertility and Sterility. 99(7). 1831–1837. 24 indexed citations

10.

Quaynor, Samuel D., et al.. (2013). Differential expression of nasal embryonic LHRH factor (NELF) variants in immortalized GnRH neuronal cell lines. Molecular and Cellular Endocrinology. 383(1-2). 32–37. 5 indexed citations

11.

Layman, Lawrence C., Sandra P.T. Tho, Andrew Clark, Anita S. Kulharya, & Paul G. McDonough. (2008). Phenotypic spectrum of 45,X/46,XY males with a ring Y chromosome and bilaterally descended testes. Fertility and Sterility. 91(3). 791–797. 52 indexed citations

12.

Layman, Lawrence C.. (2003). Genetic causes of human infertility. Endocrinology and Metabolism Clinics of North America. 32(3). 549–572. 15 indexed citations

13.

Layman, Lawrence C.. (2002). Human gene mutations causing infertility. Journal of Medical Genetics. 39(3). 153–161. 81 indexed citations

14.

Layman, Lawrence C.. (2000). Mutations in the Follicle-Stimulating Hormone-Beta (FSHβ) and FSH Receptor Genes in Mice and Humans. Seminars in Reproductive Medicine. 18(1). 5–10. 29 indexed citations

15.

Layman, Lawrence C.. (1999). Genetics of human hypogonadotropic hypogonadism. American Journal of Medical Genetics. 89(4). 240–248. 38 indexed citations

16.

Taylor, Hugh S., et al.. (1999). Mutation analysis of the EMX2 gene in Kallmann’s syndrome. Fertility and Sterility. 72(5). 910–914. 9 indexed citations

17.

Layman, Lawrence C., et al.. (1998). Use of denaturing gradient gel blots to screen for point mutations in the factor VIII gene. Human Mutation. 12(6). 393–402. 6 indexed citations

18.

Layman, Lawrence C., Eun Jig Lee, Anne B. Namnoum, et al.. (1997). Delayed Puberty and Hypogonadism Caused by Mutations in the Follicle-Stimulating Hormone β-Subunit Gene. New England Journal of Medicine. 337(9). 607–611. 179 indexed citations

19.

Layman, Lawrence C., et al.. (1995). The follicle-stimulating hormone receptor gene is polymorphic in premature ovarian failure and normal controls. Fertility and Sterility. 64(3). 518–524. 45 indexed citations

20.

Layman, Lawrence C., et al.. (1992). Gonadotropin-releasing hormone-associated peptide gene sequences in women with hyperprolactinemia. Fertility and Sterility. 58(5). 908–913. 1 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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