Search Results - "Epstein MP"

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.

Authors: Trevino CE Holleman AM Corbitt H et al.

Source: Scientific reports [Sci Rep] 2021 Jul 20; Vol. 11 (1), pp. 15164. Date of Electronic Publication: 2021 Jul 20.

Publication Type: Published Erratum

Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN: 2045-2322 (Electronic) Linking ISSN: 20452322 NLM ISO Abbreviation: Sci Rep Subsets: MEDLINE; PubMed not MEDLINE

Identifying condition-related cell-cell communication events using supervised tensor analysis.

Authors: Dai Q Yang J Epstein MP

Source: American journal of human genetics [Am J Hum Genet] 2026 Jul 02; Vol. 113 (7), pp. 1495-1508. Date of Electronic Publication: 2026 Jun 04.

Publication Type: Journal Article

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Expectations for papers performing Mendelian randomization analyses.

Authors: Williams SM Tang H Cooper GM et al.

Source: PLoS genetics [PLoS Genet] 2025 Jul 17; Vol. 21 (7), pp. e1011767. Date of Electronic Publication: 2025 Jul 17 (Print Publication: 2025).

Publication Type: Editorial

Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE; In Process

Multi-tissue transcriptome-wide association study identifies 29 risk genes associated with attention-deficit/hyperactivity disorder.

Authors: Abrishamcar S Dai Q Yang J et al.

Source: MedRxiv : the preprint server for health sciences [medRxiv] 2026 Feb 22. Date of Electronic Publication: 2026 Feb 22.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE

Integrative transcriptome-wide association analyses reveal PRKCG-linked GABAergic dysfunction in Fragile X-associated tremor/ataxia syndrome.

Authors: Jin Y Cao Y Ma W et al.

Source: Nature communications [Nat Commun] 2026 Jan 08; Vol. 17 (1), pp. 1418. Date of Electronic Publication: 2026 Jan 08.

Publication Type: Journal Article

Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios.

Authors: Robinson KR Curtis SW Paschall JE et al.

Source: American journal of human genetics [Am J Hum Genet] 2025 Nov 06; Vol. 112 (11), pp. 2679-2692. Date of Electronic Publication: 2025 Oct 06.

Publication Type: Journal Article; Research Support, N.I.H., Extramural

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Multiancestry brain pQTL fine-mapping and integration with genome-wide association studies of 21 neurologic and psychiatric conditions.

Authors: Wingo AP Liu Y Vattathil SM et al.

Source: Nature genetics [Nat Genet] 2025 Sep; Vol. 57 (9), pp. 2156-2165. Date of Electronic Publication: 2025 Sep 08.

Publication Type: Journal Article

Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE

CADET: Enhanced transcriptome-wide association analyses in admixed samples using eQTL summary data.

Authors: Head ST Dai Q Schildkraut J et al.

Source: American journal of human genetics [Am J Hum Genet] 2025 Jul 03; Vol. 112 (7), pp. 1580-1596. Date of Electronic Publication: 2025 Jun 13.

Publication Type: Journal Article; Research Support, N.I.H., Extramural

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Identifying condition-related cell-cell communication events using supervised tensor analysis.

Authors: Dai Q Yang J Epstein MP

Source: BioRxiv : the preprint server for biology [bioRxiv] 2025 Jun 19. Date of Electronic Publication: 2025 Jun 19.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101680187 Publication Model: Electronic Cited Medium: Internet ISSN: 2692-8205 (Electronic) Linking ISSN: 26928205 NLM ISO Abbreviation: bioRxiv Subsets: PubMed not MEDLINE

Proteome-wide association studies using summary pQTL data of brain, CSF, and plasma identify 30 risk genes of Alzheimer's disease dementia.

Authors: Hu T Liu Q Dai Q et al.

Source: Alzheimer's research & therapy [Alzheimers Res Ther] 2025 Jun 18; Vol. 17 (1), pp. 135. Date of Electronic Publication: 2025 Jun 18.

Publication Type: Journal Article

Journal Info: Publisher: BioMed Central Ltd Country of Publication: England NLM ID: 101511643 Publication Model: Electronic Cited Medium: Internet ISSN: 1758-9193 (Electronic) NLM ISO Abbreviation: Alzheimers Res Ther Subsets: MEDLINE

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 trios.

Authors: Robinson KR Curtis SW Paschall JE et al.

Source: MedRxiv : the preprint server for health sciences [medRxiv] 2025 Mar 04. Date of Electronic Publication: 2025 Mar 04.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE

Rare variants in PRKCI cause Van der Woude syndrome and other features of peridermopathy.

Authors: Robinson K Singh SK Walkup RB et al.

Source: MedRxiv : the preprint server for health sciences [medRxiv] 2025 Jan 17. Date of Electronic Publication: 2025 Jan 17.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE

Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of bias.

Authors: Ellis CA Oliver KL Harris RV et al.

Source: American journal of human genetics [Am J Hum Genet] 2024 Sep 05; Vol. 111 (9), pp. 1805-1809. Date of Electronic Publication: 2024 Aug 20.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Omnibus proteome-wide association study identifies 43 risk genes for Alzheimer disease dementia.

Authors: Hu T Parrish RL Dai Q et al.

Source: American journal of human genetics [Am J Hum Genet] 2024 Sep 05; Vol. 111 (9), pp. 1848-1863. Date of Electronic Publication: 2024 Jul 29.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Proteome-wide association studies using summary pQTL data of three tissues identified 30 risk genes of Alzheimer's disease dementia.

Authors: Hu T Liu Q Dai Q et al.

Source: MedRxiv : the preprint server for health sciences [medRxiv] 2024 Sep 04. Date of Electronic Publication: 2024 Sep 04.

Publication Type: Journal Article; Preprint

Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE

Cis- and trans-eQTL TWASs of breast and ovarian cancer identify more than 100 susceptibility genes in the BCAC and OCAC consortia.

Authors: Head ST Dezem F Todor A et al.

Source: American journal of human genetics [Am J Hum Genet] 2024 Jun 06; Vol. 111 (6), pp. 1084-1099. Date of Electronic Publication: 2024 May 08.

Publication Type: Journal Article

Journal Info: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

Novel Variance-Component TWAS method for studying complex human diseases with applications to Alzheimer's dementia.

Authors: Tang S Buchman AS De Jager PL et al.

Source: PLoS genetics [PLoS Genet] 2021 Apr 02; Vol. 17 (4), pp. e1009482. Date of Electronic Publication: 2021 Apr 02 (Print Publication: 2021).

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101239074 Publication Model: eCollection Cited Medium: Internet ISSN: 1553-7404 (Electronic) Linking ISSN: 15537390 NLM ISO Abbreviation: PLoS Genet Subsets: MEDLINE

Cis- and trans-eQTL TWAS of breast and ovarian cancer identify more than 100 risk associated genes in the BCAC and OCAC consortia.

Authors: Head ST Dezem F Todor A et al.

Source: BioRxiv : the preprint server for biology [bioRxiv] 2023 Nov 13. Date of Electronic Publication: 2023 Nov 13.

Publication Type: Preprint; Journal Article

Journal Info: Country of Publication: United States NLM ID: 101680187 Publication Model: Electronic Cited Medium: Internet ISSN: 2692-8205 (Electronic) Linking ISSN: 26928205 NLM ISO Abbreviation: bioRxiv Subsets: PubMed not MEDLINE

Rare variants found in clinical gene panels illuminate the genetic and allelic architecture of orofacial clefting.

Authors: Diaz Perez KK Curtis SW Sanchis-Juan A et al.

Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2023 Oct; Vol. 25 (10), pp. 100918. Date of Electronic Publication: 2023 Jun 15.

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE

Rare genetic variants in SEC24D modify orofacial cleft phenotypes.

Authors: Curtis SW Carlson JC Beaty TH et al.

Source: MedRxiv : the preprint server for health sciences [medRxiv] 2023 Mar 27. Date of Electronic Publication: 2023 Mar 27.

Publication Type: Preprint; Journal Article

Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE