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| Research Topics: |
| INDEX |
| AI-chat 1 |
| PRIME 37 |
| aging 12 |
| body 2 |
| brain 17 |
| brainwave 3 |
| cancer 7 |
| climate 3 |
| cognition 10 |
| covid-19 6 |
| crime 3 |
| culture 3 |
| diabetes 6 |
| diagnostics 2 |
| disease 3 |
| drugs 1 |
| energy 1 |
| exercise 3 |
| eyes 1 |
| genetics 12 |
| gut 3 |
| heart 15 |
| immune 8 |
| kidneys 5 |
| language 2 |
| metabolism 2 |
| microbiome 2 |
| nutrition 11 |
| obesity 2 |
| physical 2 |
| politics 2 |
| pollution 2 |
| population 2 |
| practice 2 |
| privacy 2 |
| psychology 14 |
| quantum 1 |
| reproduction 2 |
| rights 1 |
| sleep 2 |
| space 1 |
| tech 2 |
| unk |
| vaccine 2 |
| virus 2 |
| war-confl |
| war-cyber 1 |
|
Scanned: 3012 Evaluated: 322 Selected: 92 |
| GENETICS   POPULATION   REPRODUCTION | |||||||||||||||||||
Mep32-021 | Population Differences in the Epidemiology, Phenotype, and Genetics of Hirschsprung Disease in the United States | ||||||||||||||||||
| Quote: | Genetically, the major difference in Blacks is the unique association with noncoding regulatory variation at the SOX10 gene not observed in Whites. Meaning These findings uncover significant population differences in incidence and clinical presentation, but limited qualitative but greater quantitative genetic differences, in Hirschsprung disease. Beyond being useful for understanding HSCR natural history and for genetic counseling, it begs for research on the causes of the variable frequency and presentations across populations. | ||||||||||||||||||
| Abstract: | https://www.medrxiv.org/content/10.64898/2026.08.10.26360052v1 | ||||||||||||||||||
| Full Text: | https://www.medrxiv.org/content/10.64898/2026.08.10.26360052v1.full-text | ||||||||||||||||||
| Search Similar: | Brave Mojeek Startpage Dogpile Bing Googl Lycos Utub Yaho | ||||||||||||||||||
| Search Authors: | Mingzhou Fu Hanna E Berk-Rauch Monica Erazo Sumantra Chatterjee Aravinda Chakravarti, | ||||||||||||||||||
| Search Words: |
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| AGING   REPRODUCTION | |||||||||||||||||||
Mge32-002 | The Xella Clock: a female-specific epigenetic aging clock optimized for menstrual fluid and endometrial tissue | ||||||||||||||||||
| Quote: | Our model, the Xella Clock, outperforms other widely used epigenetic aging clocks at predicting chronological age from MF data and on endometrial tissue. The model is a useful tool for advancing the study of female reproductive aging and can be used to examine associations between endometrial age acceleration and clinical factors. | ||||||||||||||||||
| Abstract: | https://www.medrxiv.org/content/10.64898/2026.08.07.26359971v1 | ||||||||||||||||||
| Full Text: | https://www.medrxiv.org/content/10.64898/2026.08.07.26359971v1.full-text | ||||||||||||||||||
| Search Similar: | Brave Mojeek Startpage Dogpile Bing Googl Lycos Utub Yaho | ||||||||||||||||||
| Search Authors: | Ananya Pavuluri Billie Gould Amit Indap Nadiia Salakh Kelly Lacob Adriana Dantas Olga Sazonova Jesus Ching, | ||||||||||||||||||
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Javilk's Research Links Newsletter for Week 32 Updated 08/15/2026-01:24:35 AM What interests you? What have you found? Tell me! Drop me a note to subscribe or submit something. |