Ave M. Lachiewicz

2.7k total citations
38 papers, 1.9k citations indexed

About

Ave M. Lachiewicz is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology. According to data from OpenAlex, Ave M. Lachiewicz has authored 38 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 26 papers in Cognitive Neuroscience and 10 papers in Molecular Biology. Recurrent topics in Ave M. Lachiewicz's work include Genetics and Neurodevelopmental Disorders (32 papers), Autism Spectrum Disorder Research (25 papers) and Congenital heart defects research (6 papers). Ave M. Lachiewicz is often cited by papers focused on Genetics and Neurodevelopmental Disorders (32 papers), Autism Spectrum Disorder Research (25 papers) and Congenital heart defects research (6 papers). Ave M. Lachiewicz collaborates with scholars based in United States, Australia and Sweden. Ave M. Lachiewicz's co-authors include Deborah V. Dawson, Gail A. Spiridigliozzi, Elizabeth Berry‐Kravis, Allyn McConkie‐Rosell, Randi J. Hagerman, Jeannie Visootsak, Carol Delahunty, Walter E. Kaufmann, David Hessl and Jonathan Picker and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Journal of the American Academy of Child & Adolescent Psychiatry.

In The Last Decade

Ave M. Lachiewicz

38 papers receiving 1.8k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ave M. Lachiewicz United States	23	1.6k	1.2k	784	242	153	38	1.9k
Jennifer Reichert United States	15	1.5k 1.0×	1.6k 1.3×	869 1.1×	166 0.7×	256 1.7×	17	2.3k
Jeannie Visootsak United States	26	2.0k 1.3×	1.1k 0.9×	1.2k 1.6×	212 0.9×	173 1.1×	54	2.7k
Evald Sæmundsen Iceland	16	1.3k 0.8×	1.2k 1.0×	566 0.7×	380 1.6×	358 2.3×	26	2.0k
Sarojini Budden United States	22	1.2k 0.8×	794 0.7×	788 1.0×	271 1.1×	237 1.5×	30	1.7k
Sarika U. Peters United States	29	2.1k 1.3×	915 0.8×	1.3k 1.6×	208 0.9×	213 1.4×	63	2.7k
Guiomar Oliveira Portugal	20	751 0.5×	1.0k 0.8×	427 0.5×	173 0.7×	291 1.9×	91	1.6k
Daniel Braunschweig United States	16	817 0.5×	1.1k 1.0×	303 0.4×	142 0.6×	278 1.8×	16	1.8k
Donna M. Werling United States	12	735 0.5×	978 0.8×	383 0.5×	254 1.0×	230 1.5×	18	1.6k
Richard J. Simensen United States	21	1.2k 0.8×	638 0.5×	912 1.2×	103 0.4×	52 0.3×	50	1.9k
T. Webb United Kingdom	24	2.1k 1.4×	940 0.8×	904 1.2×	152 0.6×	56 0.4×	60	2.4k

Countries citing papers authored by Ave M. Lachiewicz

Since Specialization

Citations

This map shows the geographic impact of Ave M. Lachiewicz'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 Ave M. Lachiewicz with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ave M. Lachiewicz more than expected).

Fields of papers citing papers by Ave M. Lachiewicz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ave M. Lachiewicz. 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 Ave M. Lachiewicz. The network helps show where Ave M. Lachiewicz may publish in the future.

Co-authorship network of co-authors of Ave M. Lachiewicz

This figure shows the co-authorship network connecting the top 25 collaborators of Ave M. Lachiewicz. A scholar is included among the top collaborators of Ave M. Lachiewicz 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 Ave M. Lachiewicz. Ave M. Lachiewicz 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

Lachiewicz, Ave M., Tracy Stackhouse, Howard Andrews, et al.. (2023). Sensory Symptoms and Signs of Hyperarousal in Individuals with Fragile X Syndrome: Findings from the FORWARD Registry and Database Multisite Study. Journal of Autism and Developmental Disorders. 54(11). 4259–4277. 4 indexed citations

Spiridigliozzi, Gail A., Tatyana Adayev, Allyn McConkie‐Rosell, et al.. (2023). High performing male with fragile X syndrome with an unmethylated FMR1 full mutation: The relevance of clinical and genetic correlations. SHILAP Revista de lepidopterología. 11(6). e7371–e7371. 3 indexed citations

Markunas, Christina A., Ann L. Collins, Melanie E. Garrett, et al.. (2010). Genetic variants in SLC9A9 are associated with measures of Attention-deficit/hyperactivity disorder symptoms in families. Psychiatric Genetics. 20(2). 73–81. 37 indexed citations

Lachiewicz, Ave M., et al.. (2010). Indicators of anxiety and depression in women with the fragile X premutation: assessment of a clinical sample. Journal of Intellectual Disability Research. 54(7). 597–610. 22 indexed citations

Kollins, Scott H., Melanie E. Garrett, F. Joseph McClernon, et al.. (2009). Effects of Postnatal Parental Smoking on Parent and Teacher Ratings of ADHD and Oppositional Symptoms. The Journal of Nervous and Mental Disease. 197(6). 442–449. 15 indexed citations

Kollins, Scott H., et al.. (2008). SNPs in dopamine D2 receptor gene (DRD2) and norepinephrine transporter gene (NET) are associated with continuous performance task (CPT) phenotypes in ADHD children and their families. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(8). 1580–1588. 55 indexed citations

McConkie‐Rosell, Allyn, Gail A. Spiridigliozzi, Jennifer A. Sullivan, Deborah V. Dawson, & Ave M. Lachiewicz. (2002). Carrier testing in fragile X syndrome: When to tell and test. American Journal of Medical Genetics. 110(1). 36–44. 24 indexed citations

Tassone, Flora, Randi J. Hagerman, Danuta Z. Loesch, et al.. (2000). Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels ofFMR1 messenger RNA. American Journal of Medical Genetics. 94(3). 232–236. 120 indexed citations

McConkie‐Rosell, Allyn, Gail A. Spiridigliozzi, Jennifer A. Sullivan, Deborah V. Dawson, & Ave M. Lachiewicz. (2000). Carrier testing in fragile X syndrome: Effect on self-concept. American Journal of Medical Genetics. 92(5). 336–342. 27 indexed citations

10.

McConkie‐Rosell, Allyn, Gail A. Spiridigliozzi, Jennifer A. Sullivan, Deborah V. Dawson, & Ave M. Lachiewicz. (2000). Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping. American Journal of Medical Genetics. 98(1). 37–45. 29 indexed citations

11.

Hatton, Deborah D., et al.. (1998). Ocular status of boys with fragile X syndrome: A prospective study. Journal of American Association for Pediatric Ophthalmology and Strabismus. 2(5). 298–302. 21 indexed citations

12.

McConkie‐Rosell, Allyn, Gail A. Spiridigliozzi, Timothy Iafolla, Jack Tarleton, & Ave M. Lachiewicz. (1997). Carrier testing in the fragile X syndrome: Attitudes and opinions of obligate carriers. American Journal of Medical Genetics. 68(1). 62–69. 48 indexed citations

13.

Lachiewicz, Ave M., Gail A. Spiridigliozzi, Allyn McConkie‐Rosell, et al.. (1996). A fragile X male with a broad smear on southern blot analysis representing 100–500 CGG repeats and no methylation at theEagI site of the FMR-1 gene. American Journal of Medical Genetics. 64(2). 278–282. 18 indexed citations

14.

Dykens, Elisabeth M., Sharon Ort, Ira S. Cohen, et al.. (1996). Trajectories and profiles of adaptive behavior in males with fragile X syndrome: Multicenter studies. Journal of Autism and Developmental Disorders. 26(3). 287–301. 42 indexed citations

15.

Lachiewicz, Ave M. & Deborah V. Dawson. (1994). Behavior problems of young girls with fragile X syndrome: Factor scores on the Conners' parent's questionnaire. American Journal of Medical Genetics. 51(4). 364–369. 34 indexed citations

16.

Albright, Susan G., Ave M. Lachiewicz, Jack Tarleton, et al.. (1994). Fragile X phenotype in a patient with a large de novo deletion in Xq27‐q28. American Journal of Medical Genetics. 51(4). 294–297. 17 indexed citations

17.

McConkie‐Rosell, Allyn, Ave M. Lachiewicz, Gail A. Spiridigliozzi, et al.. (1993). Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.. PubMed. 53(4). 800–9. 138 indexed citations

18.

Lachiewicz, Ave M., et al.. (1991). Association of the Robin sequence with the fragile X syndrome. American Journal of Medical Genetics. 41(3). 275–278. 6 indexed citations

19.

Lachiewicz, Ave M., et al.. (1991). Townes—Brocks syndrome in two mentally retarded youngsters. American Journal of Medical Genetics. 41(1). 1–4. 21 indexed citations

20.

Lachiewicz, Ave M., Richard Sibley, & Alfred F. Michael. (1985). Hereditary renal disease and preauricular pits: Report of a kindred. The Journal of Pediatrics. 106(6). 948–950. 4 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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