Results 81 to 90 of about 68,163 (301)

ResearchConnect: An AI‐Powered Platform for Interdisciplinary Research Team Formation and Ideation Development

Advanced Intelligent Systems, EarlyView.
ResearchConnect is an AI‐powered platform that automates researcher profiling, interdisciplinary team formation, and early‐stage research ideation. By extracting keywords from papers and web sources, it quickly clusters researchers into coherent teams and generates collaborative ideas using large language models. Validation on NSF‐funded projects shows
Akshay Vilas Jadhav, Milad Masrouri, Zhao Qin   +2 more
wiley   +1 more source

Australian Sphingidae – DNA Barcodes Challenge Current Species Boundaries and Distributions [PDF]

, 2014
© 2014 Rougerie et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are ...
A Hausmann, A Hausmann, A Riedel, AD Austin, Axel Hausmann, Ben J. Mans, BR Scheffers, D Lane, D Romero, DC Lees, DC Lees, DR Vieites, EJV Nieukerken, HCJ Godfray, I Letunic, Ian J. Kitching, J Beck, J Marin, JCE Riotte, JD Holloway, Jean Haxaire, JF Landry, JM Padial, JP Tuttle, K Tamura, M Kimura, M Mutanen, MA Smith, MI Krzywinski, MS Moulds, NP Kristensen, P Darge, P Sharma, Paul D. N. Hebert, PD Hebert, PDN Hebert, PDN Hebert, PDN Hebert, PM Oliver, PS Cranston, PS Gehring, PZ Goldstein, R Brechlin, R Brechlin, R Rougerie, R Rougerie, RM May, Rodolphe Rougerie, S Ratnasingham, S Ratnasingham, S Wakamura, Scott E. Miller, SW James, T Vaglia, U Eitschberger   +54 more
core   +4 more sources

Differentiating the Clinical and Variant Spectrum of Hardikar Syndrome From Other MED12‐Related Developmental Disorders

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The rare X‐linked female‐restricted Hardikar syndrome (HDKR, OMIM # 301068) is characterized by multiple congenital anomalies including orofacial clefts, gastrointestinal, genitourinary, and cardiac anomalies, but cognitive and neurobehavioral development is rarely impaired.
Tinne Warmoeskerken, Miel Theunis, Kris Van den Bogaert, Koenraad Devriendt, Jeroen Breckpot   +4 more
wiley   +1 more source

New records, nomenclatural changes, and taxonomic notes for select North American leaf beetles (Coleoptera: Chrysomelidae) [PDF]

, 2001
New records, nomenclatural changes and taxonomic notes are presented for select North American leaf beetles (Coleoptera: Chrysomelidae). The following genera are newly recorded from the United States: Nesaecrepida Blake, 1964; Acallepitrix Bechyne, 1959;
Clark, Shawn M., Gilbert, Arthur J., Riley, Edward G.   +2 more
core   +1 more source

A Systematic Review of Adverse Childhood Experiences and Epigenetic Age Acceleration in Later Adult Life Measured With Second and Third‐Generation Epigenetic Clocks

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, EarlyView.
ABSTRACT We examined the relationship between adverse childhood experiences (ACEs) and epigenetic age acceleration (EAA) in adulthood as measured by second and third generation epigenetic clocks by performing a systematic review of the literature. The electronic databases MEDLINE and EMBASE were searched on 17 July 2023.
Matthew Green, Laura Horsfall, Azam Saied   +2 more
wiley   +1 more source

Clustering and Latent Semantic Indexing Aspects of the Nonnegative Matrix Factorization [PDF]

, 2011
This paper provides a theoretical support for clustering aspect of the nonnegative matrix factorization (NMF). By utilizing the Karush-Kuhn-Tucker optimality conditions, we show that NMF objective is equivalent to graph clustering objective, so ...
Mirzal, Andri
core  

Genome Sequencing in 19 Families With Bladder Exstrophy and Epispadias Complex Indicates Involvement of the ADGR‐Gene Family

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Bladder exstrophy and epispadias complex (BEEC) is one of the most severe congenital malformations of the urogenital tract, significantly impacting continence, sexual function, and renal function. To date, the only recurrent genetic aberration identified is the 22q.11.2 microduplication, but several candidate regions and genes including ...
Agneta Nordenskjöld, Samara Alm, Jesper Eisfeldt, Jia Cao, Magnus Anderberg, Gillian Barker, Hans Matsson, Gundela Holmdahl, Anna Lindstrand, Kristina Lagerstedt‐Robinson   +9 more
wiley   +1 more source

Corrections, clarifications, and additions to the 1996 checklist of the Alticinae of Central America : including Mexico (Coleoptera: Chrysomelidae) [PDF]

, 1998
In our checklist of the Alticinae of Central America and Mexico (Furth and Savini, 1996), there were some species whose status or generic combination needs clarification.
Furth, David G., Savini, Vilma
core   +1 more source

The Insistence of Blackness and the Persistence of Antiblackness in Ireland

Australian Journal of Social Issues, EarlyView.
ABSTRACT This paper positions Ireland as a critical site for examining the insistence of blackness and an antiblackness created and sustained through Irish ethnonationalist imaginaries and exclusionary processes. Drawing on connected sociologies and Irish Black Studies, this enquiry argues that antiblackness in Ireland operates as a generational force,
Philomena Mullen
wiley   +1 more source

Revision of the genus Teratolytta (Coleoptera: Meloidae)

European Journal of Entomology, 2006
The blister beetle genus Teratolytta, belonging to the tribe Lyttini, is revised and a classification is proposed. Two main sections of the genus - one including five groups of species and the other three groups - are tentatively defined.
Marco A. BOLOGNA, Andrea DI GIULIO
doaj   +1 more source